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Saturday, 29 October 2011

Pharmaceutical Expo 2011 - Pharma Exhibition 2011 (Banglore) - 16 December 2011

Name:        PHARMAceutical Expo 2011
Date:          16 Dec 2011 - 18 Dec 2011
Venue:       Banglore International Exhibition Center, Banglore, India
Organizer: Federation of Indian Chamber of Commerce and Pharmaceutical Congress

About Pharmaceutical Expo 2011:

Federation of Indian Chamber of Commerce and Industry (FICCI) concurrent with the 63rd Indian Pharmaceutical Congress (IPC) organizing PHARMACEUTICAL  EXPO 2011 at Bangalore International Exhibition Center, Bangalore from December 16-18, 2011. 



Highlights:
  • 10,000 sq mtrs of exhibition area
  • More than 200 exhibitors
  • Only focused event on Pharmaceutical Industry
  • More than 8000 delegates attending the congress, that means a focused target audience for the exhibition
  • Networking opportunities
  • Excellent facilities of Business Centre, Lounge, Exhibitors Restaurant, Snack Counters, Drinking Water, Information Desk, Travel & Transport Desk, Business Information Centre, etc.

For more info "Click Here"


Friday, 21 October 2011

Nano Medicine 2011 - BIT's 2nd Annual World Congress of NanoMedicine-2011

Name:        BIT's 2nd Annual World Congress of NanoMedicine-2011
Date:          3 Nov 2011 - 5 Nov 2011
Venue:       Shenzhen Convention & Exhibition Center
Organizer: BIT Life Sciences
email:         eva@bitconferences.com


High lights of Nano Medicine 2011 - conference

  • 1 Plenary Forum from a panel of leading experts in Nanomedicine
  • 6 Parallel Scientific symposia with 91 Sessions on breaking research to industrial development
  • 300-400 Oral Presentations by top level engineers and scientists in Nanomedicine
  • 50+ Poster presentations for updating current Nanomedical R & D
  • 1 Product and Service Exhibition with 40-50 Companies along the meeting period
  • 1000+ Participants from active groups and parties in Nanotechnology and Medicine
  • 2 Social Events for network with potential partners and customers
  • 1 Tech Tour to the beautiful cities in China
Nano Medicine market Trends:

The world nanomedicine market is suggested to surpass $160 Billion by the year 2015. This huge market demand has provided unprecedented space for innovators and industrial developmers to push the limit of Nanotechnology fully applied for diversified medical fields as many as possible. This congress including six parallel scientific symposia will energize your great passions to showcase the most recently breaking research, discovery and industrial milestones in Nanomedicinal R & D and Business development. As a co-current meeting to BIT’s 9th Drug Discovery Congress, i.e. IDDST-2011, and the 1st Drug Delivery System Congress, this year Nanomedicine congress will offer you huge opportunities for catching the fast growing market trend and collaborative business potential through the dynamic scientific and social activities along the events with our colleagues.
(Source: Bit Conference)



Wednesday, 21 September 2011

IV International conference - Extractables and Leachables for Pharmaceutical Products 2011

Exhibition for Pharma Products "Extractables and Leachables"



Pharma Industry Exhibition Name: Extractables and Leachables for Pharmaceutical Products 2011
Venue: Dublin, Ireland
Date: 27 - 28 Sept 2011
Contact No: + 44 (0)1939 250383
Conference Language: English


The " Extractables and Leachables for Pharmaceutical Products 2011" would be helpful for Pharma manufacturers. This Pharma Exhibition covers


  •     Regulatory updates on extractables and leachables
  • Strategies for minimising risk
  •  Medical grade polymers
  • Implantables and their packaging
  • Innovations in processing technologies
  • Managing risk with extractables and leachables
  • Controlled extraction studies and routine extractables testing
  • Leachables studies
  •  Analytical techniques used to determine leachables and extractables
  • Biological evaluation by chemical characterisation
  • E&L implications on raw material suppliers
  • The convertor’s role in E&Ls
  • Drug manufacturers’ E&L considerations
  • N-1, N-2, N-3 case studies    



Friday, 26 August 2011

World Meet Of The Pharma & Biotech Industry In India


Name : World Meet Of The Pharma & Biotech Industry In India

Date: Feb 23-26,2011
Venue: Bombay exhibition centre,NSE complex,Goregaon,Mumbai,India


PHARMA WORLD EXPO 2011 will be 25th exhibitions, and is expected to witness record participation.
The event, supported by CHEMTECH Foundation, will display state-of-the-art technologies, equipment, accessories and services from national and international players in each sector. The concurrent International Conferences will deleberate on issues of topical interest to practising professionals.

Catalysing Industrial Growth


The evolution and the growth of Indian Pharmaceutical and Biotech industries have been both reflected and catalyzed by CHEMTECH.

Industry Poised for High Growth


The Rs 25,000 crore (USD 5 billion) Pharma Industry has an average growth rate of 9% over the last 5 years, with exports of USD 1.75 billion. The industry is a net exporter having 8% market share (in volume terms) of the USD 340 billion global market. It is rapidly restructuring to the post-2005 product patent regime.
With liberalized economy, the Pharma multinationals are expanding operations in India and Indian companies are increasingly setting up operations and entering into joint ventures in other countries.
India has some 800 companies in the biotech sector, but over 25 companies operating in the third generation modern biotechnology. With governments are backing the industry, a sizeable number of biotech parks are coming up. India, therefore, will continue to have an exponential growth in this sector as investments in research.

Wednesday, 10 August 2011

2nd Annual Medical Management in Medicare Advantage: Payer/Provider Collaborative Care Summit

Pharmaceutical Exhibition Name: 2nd Annual Medical Management in Medicare Advantage: Payer/Provider Collaborative Care Summit 
Date: August 25-26, 2011
Venue: Hyatt Regency Mission Bay Spa and Marina, San Diego, CA






Summit Details: 


More than 200 attendees at our establish event, our Collaborative Care Summit has established itself as one of the prestigious  Medical Management conferences. Our 2011 program will keep going to allow the "next generation" medical management tactics that Health Plans, Hospitals and Physician Group's require in the current economic climate.


As the chronically ill catch up with more of the Medicare Advantage population, hospital readmissions have become a significant financial challenge. Plans must have a medical management strategy i.e. grounded in:

  • Evidence-based clinical practices
  • Predictive outcomes modeling
  • Member engagement
  • Multi-disciplinary professional collaboration 

Our event will discuss:

  • Accountable Care Organizations
  • Medical Homes 
  • Transitional Care 
  • And more!
For More Info Please Click On this Link or Click Here to get Info as mail

Link:


Tuesday, 9 August 2011

Pharma Industry Survey: Still not budgeting precisely - Pharma Survey - 57% still relying on Excel spreadsheets


The pharmaceutical industry is spending $68 billion per annum on research and development, but that isn’t stopping it from continuing to cling to Excel spreadsheets as the preferred planning tool for trials.
That’s according to a new survey from ClearTrial, a company that makes budgeting software for the life sciences industry. Of the survey’s 187 responses from pharma companies large and small, 57% reported using Microsoft Excel as the predominant method for clinical study forecasting and budgeting. Not surprisingly, then, only 21% of respondents said they were highly confident in their budget forecasts.
“The tools in the industry are pretty inadequate for the type of planning that is occurring; these trials are millions or tens of millions of dollars,” said Andy Grygiel, marketing manager for ClearTrial.
Half of the respondents reported an 11% difference between what they originally thought a trial would cost and what it actually ended up costing the company. And 20% said their cost variance was 16% or more.
When ClearTrial launched in 2004, said Grygiel, there was little interest among pharma companies in taking innovative measures to budget for trials. The money was flowing and no one was too worried about accurate budgeting, he said. But flash forward seven years to a post-recession world, and Grygiel says he thought he’d see something different. Unfortunately, he hasn’t. Pharma and device companies still hold fast to tools that clearly aren’t hitting the mark—for budgeting and forecasting or anything else.
Said Grygiel, beyond Excel spreadsheets, many in the industry are also fond of spawning their own software in-house to handle operations such as budgeting. Many others purchase an off-the-shelf program and try to tailor it to conform to the vagaries of clinical trials. Others look to benchmarking databases to help them figure out what a trial will cost, doing what Grygiel calls “what-if analysis.” None of these are working well.
Those who watch the industry say this is no shocker. “I’m not surprised; the clinical research drug industry has not been a leader in adopting new technology,” said Michael Martorelli, director at investment banking firm Fairmount Partners, consultant to the CRO industry, a long-time watcher of the space and an adjunct professor of finance at Drexel University.
Initially, he said, the pharmaceutical industry was so flush, there was no need to tinker with technology that might make it more efficient. Since all that has begun to change, though, adoption of technology has been slow due to a few confounding factors. Unlike other industries that have seen much earlier adoption of technology, drug developers are heavily regulated, and have to get much of what they’re doing approved by the FDA before it happens. This has made many drug companies less likely to move toward the full-scale operational change that would come with broad, sweeping new software systems, said Martorelli. In addition, he added, the drug development process involves so many players, each with their own software and/or operational processes that don’t necessarily communicate with each other—that it can be tempting for sponsors to just take the easy route, using Excel spreadsheets or their own home-grown systems.
“Another factor,” said Martorelli, “is the long-term nature of the industry’s projects. A trial might take 15 years from start to finish, and adopting new technology in the middle of it can present a daunting mess.” Many sponsors are using new technology for their new trials, but staying old-school (think Excel) for their older ones, thus creating a mishmash of operational styles even within one company, he said.
Another spreadsheet-driven gap that the survey unearthed lie in planning efficiency. Eighty three percent of respondents said that they required at least one to two weeks to create a ballpark budget for a clinical study, while half said they needed three weeks or more. And 62% of respondents reported requiring at least three weeks to roll up individual study budgets into a budget portfolio. This, said Grygiel, is largely a result of not having necessary documents and tools for research at one’s fingertips, but rather spread about in paper files.
The industry’s insistence on clinging to old ways when it comes to budgeting and forecasting puts it 10 to 15 years behind similar industries, said Grygiel. The pharma industry, in contrast, has been very conservative about change, especially when it comes to adopting new tools whose return on investment can take awhile to see, said Grygiel.
The tide may be turning, though, if very gradually. Grygiel said he’s seeing a slowly growing focus on better budget forecasting and thus an uptick in ClearTrial’s business.
“At one time there wasn’t the tight scrutiny on budgets that there is now, but now companies are looking at ways to become more efficient,” he said. “They’re looking closely at budgets, and the tolerance of variance in budgets has really come down.”
The survey, titled “Industry Survey: Clinical Study Budgeting Practices and Metrics,” garnered responses from managers and 187 executives in clinical operations, outsourcing, finance and project management from 75 pharma and medical device companies in the U.S., Europe and Japan. Grygiel said ClearTrial plans to do the survey every year to carefully track improvement—or the lack thereof.

Source: Center Watch


Monday, 1 August 2011

PHARMAceutical Expo 2011- EXHIBITION ON PHARMA INDUSTRY

Pharma Exhibition Name: Pharmaceutical Expo 2011
Date: 16 Dec 2011 - 18 Dec 2011
Venue: Banglore International Exhibition Center, Banglore, India.

PHARMaceutical EXPO 2011 brings home the bacon an opportunity to the taking part companies to exhibit their products and services to the business visitors of across the world. The event will be attended by to a greater extent  6000 delegates and top management of the industry.




Organizers of Pharmaceutical Expo 2011: 

Indian Pharmaceutical Congress (IPC)
FICCI Federation of Indian Chamber of Commerce & Industry ( FICCI )

Contact for enquiries:

Mr. Kamal Bhardwaj, 
Senior Assistant Director
Mob: 9899392930
Email: kamal@ficci.com

Mr.Varun Shekhar Mittal
Research Associate
Mob: +91 7428118390
Email: varun.mittal@ficci.com   

Federation of Indian Chambers of Commerce and Industry
Federation House
Tansen Marg
New Delhi – 110001
Tel: 011 23357353, 23738760-70


Link For Exhibitor Registration: http://pharmaexpo.in/visitor-registration.php
Link For Visitor Registration: http://pharmaexpo.in/visitor-registration.php

 Source: PharmaExpo











Friday, 8 July 2011

Pharmaceutical and Clinical Trial Logistics Asia Pacific - Conference - Pharma Exhibition Info -

Title: Pharmaceutical and Clinical Trial Logistics Asia Pacific - Conference
Date: 18 July 2011 & 19 July 2011
Venue: Grand Copthorne Waterfront Hotel
              392 Havelock Road, Singapore, 169663

About  Pharmaceutical and Clinical Trial Logistics Asia Pacific - Conference
As supply departments face increasing pressure to justify and bring down prices, the focus on efficiency is becoming ever more important. Expeditiously gains to be had from forecasting right through to delivery, it's identical requirement to understand and defeat the challenges such as export delays, regulatory hurdles, and unexpected logistical problems.

Also among the key cause for high R&D costs is due to logistical failures admitting failure to recruit patients on time. The developed world is searching ways to avoid this is by moving clinical trials to emerging markets such as Asia. However by moving clinical trials to these regions other logistical problems emerge such as regulation, customs, quality assurance etc. 



 Pharmaceutical and Clinical Trial Logistics Asia Pacific - Conference will focus on all those key issues.                                                                                                                                        Pharmaceutical and Clinical Trial Logistics Asia Pacific event will discuss best strategies in achieving reliable and cost-effective supply chain and logistics systems currently being developed in the APAC region.


Why   Pharmaceutical and Clinical Trial Logistics Asia Pacific
  • Identify inefficiencies in your supply chain and develop strategies to streamline them
  • Understand the legislative requirements around pharma-logistics in the APAC region
  • Learn from and network with senior industry experts in this area
  • Explore lean manufacturing and effective supply chain management processes to expedite your processes
Who to  Pharmaceutical and Clinical Trial Logistics Asia Pacific Conference
  • Heads of Supply Chain
  • Heads of Logistics
  • Heads of Clinical Supply Operations
  • Heads of Clinical Trials Logistics
  • Heads of Clinical/Investigational Supplies
  • Heads of Shipping and Distribution
  • Heads of Clinical Labelling / Packaging
  • Heads of Clinical Trials Material Management
  • Heads of Clinical Supplies Manufacturing
  • Heads of Clinical Quality Assurance/Quality Control
  • Heads of Regulatory Affairs
  • Sourcing and Procurement Managers
For More Details and Registration "Please Click Here"


Monday, 4 July 2011

Novartis picks up FDA approval for Arcapta(TM) Neohaler(TM) - Arcapta(TM) - Neohaler(TM)

 A multinational pharmaceutical company Novartis foretold that the US Food and Drug Administration (FDA) has sanctioned once-daily Arcapta(TM) Neohaler(TM) (indacaterol inhalation powder) 75 mcg (microgram) for the long-term care bronchodilator treatment of airflow obstruction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and/or pulmonary emphysema. Arcapta isn't indicated for acute deteriorations of COPD or to cover bronchial asthma.
The determination makes Arcapta, formerly called QAB149, the 1st once-daily therapy in the long-acting beta2-agonist (LABA) class to be approved in the US for maintenance treatment of airflow obstruction in COPD patients.

"With millions of Americans experienced to be affected by COPD, the approval of Arcapta is beneficial news for patients," stated John W. Walsh, president and co-founder of the US-based COPD Foundation. "Afresh once-daily medicine is a welcome improver to the treatment selections for people suffering with this serious and debilitating disease."
Novartis Campus

Arcapta 75 mcg was analysed in a total of 641 COPD patients in two key phase III clinical trial durable 12 weeks. Results at week 12 bore witness that Arcapta significantly amended lung function at 24 hours equated to placebo. Lung function betterments were seen 5 minutes after the 1st dose and systematically maintained over 12 weeks. . Arcapta as well significantly brought down the need for patients to use daily rescue medication. Additionally, Arcapta improved health-related quality of life compared to placebo, as measured with the St George's Respiratory Questionnaire (SGRQ) . The SGRQ is widely used in clinical trials to measure symptoms, actions, and affect of COPD on daily life as reported by patients.

The clinical trial program supporting US submission evaluated safety in 2,516 patients who found Arcapta for at least 12 weeks at doses of 75 mcg or more, with results supporting the safety and tolerability profile of Arcapta. The basic harmful reactions in 449 patients taking Arcapta 75 mcg (i.e. those accounted in more than 2% of patients and with higher incidence than placebo) were cough, nasopharyngitis, headache, sickness and oropharyngeal pain.

"Novartis is concentrated on adding innovative, safe and effective COPD medicines to patients and medicos," said Trevor Mundel, MD, Global Head of Development in the Pharmaceuticals Division of Novartis. "Indacaterol is the cornerstone of our respiratory portfolio and this US ahttp://www.blogger.com/post-edit.g?blogID=876280343763131026&postID=4281756857749519552pproval represents a significant clinical and regulatory milestone."

Indacaterol was 1st sanctioned in November 2009 in the European Union under the brand-name Onbrez® Breezhaler®. It's now sanctioned in more than 60 countries for the treatment of COPD, and is available in more than 30 countries with additional launches planned during 2011. The Arcapta US launch is planned for the beginning quarter of 2012.

COPD is a progressive and dangerous lung disease that makes it difficult to breathe. More than 12 million people in the US are affected, while another estimated 12 million people are believed to have the disease but remain undiagnosed. COPD ranks as the third leading cause of death in the US,  and is a major cause of serious long-term disability. Worldwide, COPD is approximated to affect a total of 210 million people.

Source: World Pharma News

Sunday, 26 June 2011

ASCO Launches Cancer.Net Mobile, a New App for iPhone, iPad, and iPod Touch


The American Society of Clinical Oncology (ASCO), the world's leading professional organization representing cancer physicians, released Cancer.Net Mobile for the iPhone, iPad, and iPod Touch - a free app designed by oncologists to help people with cancer and their caregivers plan and manage cancer treatment and care. The app includes comprehensive, doctor-approved information on more than 120 cancer types, together with a package of interactive tools for patients. Cancer.Net Mobile is available for download in Apple's App Store and is the mobile companion to ASCO's award-winning Cancer.Net website.
"Cancer.Net Mobile puts up-to-date, accurate cancer information and interactive tools at the fingertips of people living with cancer and their families and caregivers, wherever they are," said ASCO CEO Allen S. Lichter, MD. "Cancer.Net Mobile was developed by leading cancer doctors with patients and their caregivers in mind, to help them take charge of their cancer care and get the most out of doctor's visits."


In addition to its comprehensive cancer guides covering more than 120 common and rare types of cancer, Cancer.Net Mobile includes interactive tools for patients and caregivers to:

Keep track of questions to ask their doctors, record voice answers, and choose from frequently-asked questions suggested by Cancer.Net experts
Save important information about prescribed medications, including photos of medicine labels and bottles (on camera-enabled devices)
Track the time and severity of symptoms and side effects during treatment, to aid in reporting them during doctor’s visits
Learn about new cancer care topics through weekly podcast and video interviews with ASCO member physicians
Cancer.Net Mobile offers a portable version of the extensive cancer information library available on the Cancer.Net website, with expert information about treating cancer, managing side effects, managing the cost of care, and coping with a cancer diagnosis. All Cancer.Net content is reviewed for accuracy and completeness by an editorial board composed of more than 150 medical, surgical, radiation, and pediatric oncologists; oncology nurses; social workers; and patient advocates. This ensures that the cancer information provided reflects the latest advances in cancer science and clinical practice. Cancer.Net is supported by the Conquer Cancer Foundation of ASCO.

Cancer.Net Mobile is available for download in Apple's App Store at http://itunes.com/apps/cancernetmobile (iTunes required). It is compatible with iPhone, iPad, and iPod Touch devices running iOS version 3.2 or later. Cancer.Net Mobile is a free tool provided by ASCO. Cancer.Net Mobile app updates will be issued regularly as the cancer guide content is updated.

About ASCO
The American Society of Clinical Oncology (ASCO) is the world's leading professional organization representing physicians who care for people with cancer. With nearly 30,000 members, ASCO is committed to improving cancer care through scientific meetings, educational programs, and peer-reviewed journals.

About the Conquer Cancer Foundation
The Conquer Cancer Foundation is working to create a world free from the fear of cancer by funding breakthrough research, by sharing knowledge with physicians and patients worldwide, and by supporting initiatives to ensure that all people have access to high-quality cancer care. Working in close collaboration with a global network of top scientists and clinicians, as well as leading advocacy and research organizations, the Foundation draws on the passion and expertise of the nearly 30,000 oncology professionals who are members of its partner organization, the American Society of Clinical Oncology (ASCO).

The British Pharmaceutical Industry Issues Social Media Guidance for Adverse Event Reporting


Once again the Brits have beaten the US in issuing useful guidelines for social media use by the pharmaceutical industry! As I reported back in April, 2011, the Prescription Medicines Code of Practice Authority (PMCPA), which oversees the self-regulatory code of the Association of the British Pharmaceutical Industry (ABPI), published "informal guidance" providing the drug industry advice on how to use online communications (see here).

I learned today from a tweet by @dawidge (a Pfizer employee) that the ABPI Pharmacovigilance Expert Network (PEN) published GUIDANCE NOTES ON THE MANAGEMENT OF ADVERSE EVENTS AND PRODUCT COMPLAINTS FROM PHARMACEUTICAL COMPANY SPONSORED WEBSITES (find the document here).

The guidance addresses three different ways that pharmaceutical companies may learn of adverse events (AEs) through social media:
"Listening in" -- Monitoring social media sites allows a company to "listen to" or "see" what the public are discussing, saying or sharing about the company itself, diseases, conditions, and treatment options.
"Giving out" -- Many social media sites allow companies to initiate one-way communications to deal significant messages with the public, where interactive dialogue is not permitted or practical.
"Engaging with" -- Engaging, exchanging and participating in interactive communication with the public. This type of activity is performed in both company and non-company sponsored sites.
I found a couple of interesting suggestions in these guidelines:

Companies Should Declare Involvement and Responsibilities
The guidelines state that "The company’s involvement in the social media site must be transparent to the users." Even when just "listening in," the company "should declare its presence by registering on the site using the company name." The ABPI concedes that "this may not be practicable or possible for buzz-monitoring type activities" that are usually carried out by third parties. "In addition," says ABPI, "it is also recommended that the company disclose the length of time it intends to sponsor the site (if known) and how it intends to screen and use any user-generated content."

ABPI also recommends that regulated companies "ensure that all staff involved in the social media channel are appropriately trained for performing pharmacovigilance related activities." That would include moderators and third-parties hired by the companies.

These are EXACTLY the kinds of disclosures from pharmaceutical companies that I suggested in a previous Pharma Marketing Blog post (see "Fair Social Media Practice Principles: Rules for Third-Party Engagement in Patient/Physician Social Networks" and respond to my survey).

Collecting AEs on Social Media Sites
ABPI recommends that company owned sites "be designed to facilitate the pharmacovigilance process" through use of "free text fields" and access to "internal/external reporting based tools which allow users to report suspected adverse drug reactions." One such tool might be a Adverse Event Reporting Widget (see "Using Social Media in a Crisis: Distribute a Product Safety Widget Is One Idea").

ABPI says that details of ALL AEs "should be collected and document, regardless of:
Seriousness of the event
Whether there is an identifiable reporter
Whether any adverse events are listed in the product’s Summary of Product Characteristics
Whether a definite causal relationship or link to the product has been stated
Whether the stakeholder or patient has already reported the event to the competent authority or says they have reported it to the company"
That's quite different than what commenters from the US drug industry told the FDA (see "Social Media and the Future of Adverse Event Reporting"). The US industry said such a collection regime would be too onerous.

Regarding the identity of the reporter of an AE, ABPI says an e-mail address would be considered acceptable and even a screen name would be acceptable IF the screen name allowed for contact to be made. ABPI recommends companies implement "a formal site registration process" that can be utilised to obtain information enabling regulated companies  to "identify and contact users in order to validate and follow-up on safety information." During registration, users should give consent for the company to follow-up with a user should they report AEs, says ABPI. "It should also be made clear that personal information may be processed on internal company databases and sent to regulators."

Tuesday, 31 May 2011

CPHI China - 21 to 23 June 2011- CPHI China Information - CPHI China Shanghai.

CPHI China - June 2011, Shanghai, China Information :

CPHI China @ Shanghai New Internation Expo Center (SNIEC)
Date @ 21 June 2011 to 23 June 2011
City @ Shanghai
Country @ China.

CPHI China - June 2011: Description:
CPhI China is a committed exhibition for the Medical & Pharmaceutical industry and has been organized in China since its launch in 2001. The latest edition of the fair has been organized by UBM Asia Limited and will start from 21st June 2011. Last year’s event was attended by 26, 547 pharma professionals and included 7, 806 international visitors. With such a large visitor base, this trade fair has been widely acclaimed as one of the best in the Pharmaceutical industry. CPhI China mirrors the growth of Chinese industries over the last decade and it showcases its excellence in the medical and pharma industry. With China’s initiative in the R&D and innovation, this fair opens up the doors for international exhibitors to affect an eager Chinese market. This 3 day event will happen at Shanghai New International Expo Centre.


Highlights of CPHI China - 2011

  • Trading with massive and untapped Chines market will be possible at the event.
  • Exhibit in front of global leaders and decision makers.
  • Opportunity to build important relations and partnership with other pharma companies.
  • Face to face meeting with potential customers.
  • Over 1, 600 exhibitors and 23, 000 visitors.

For More Information Please Click Here or Use this link




Monday, 30 May 2011

Optimer Pharma antibacterial drug gets Food and Drug Administration (FDA) favorable reception


Optimer Pharmaceuticals, a finder, developer and commercializer of hospital specialty products, has received the US Food and Drug Administration's (FDA) approval for its antibacterial drug Dificid (fidaxomicin) pills.

Dificid tablets are pointed for the treatment of Clostridium difficile-associated diarrhea (CDAD) in adults 18 years of age or older.

The FDA approval was given on the basis of the positive results from II Phase 3 randomized, multi-center, double-blinded trials involved 1,164 patients suffering from CDAD that compared Dificid with vancomycin, a usual antibiotic drug used to treat CDAD.

The results of the trial suggested that Dificid was higher-up to vancomycin in sustaining clinical response through 25 days on the far side the end of treatment.

Optimer president and chief executive officer(CEO) Pedro Lichtinger said the clinical development program for DIFICID was designed to address one of the greatest challenges in managing CDAD, disease recurrence.

"We are proud to provide the medical community and patients with an effective treatment proven to produce confirmed clinical response in CDAD, and are now moving into the commercialization stage where we'll partner with physicians and health systems to ensure that DIFICID reaches patients in urgent demand of an important new treatment option," Lichtinger said.http://www.pharmaexhibtion.blogspot.com

Tuesday, 26 April 2011

Diamyd Replaces CEO - Diamyd Medical - Pharmaceutical News


Diamyd Medical AB annunciates that Elisabeth Lindner today has left her position as President and chief executive officer (CEO) of the Company. Excecutive Vice President Peter Zerhouni has been appointed Acting President and CEO.

Elisabeth Lindner has left her position as President and CEO due to disagreement with the Board concerning certain important matters.

Peter Zerhouni has been involved in all aspects of the Company since 2006, including a key role in driving the Company's business and clinical trials forward. Zerhouni has a combined financial and biotechnology background, and studied at Lund University in Sweden, and University of California at Berkeley in USA. He has been working as head of business development for the last three years and played an instrumental part in securing the Company's agreement with Ortho-McNeil-Janssen Pharmaceuticals, Inc. to develop and commercialize the Diamyd® diabetes therapy.

The Board acknowledges Elisabeth Lindner's contributions to successfully progress the Phase III program with Diamyd® in recent-onset type 1 diabetes. Top line results from a European Phase III study are expected to be available later this spring. Work is currently ongoing to compile and process all the study data, which remains fully blinded to Investigators and patients as well as to Diamyd Medical AB.



About Diamyd Medical

Diamyd Medical is a Swedish pharmaceutical company focusing on the development of pharmaceuticals for the treatment of growth-onset diabetes and pain. The Diabetes business area consists of the antigen-based drug candidate Diamyd® for the treatment and prevention of autoimmune diabetes. Phase III studies of Diamyd® are currently in progress in Europe and the US. In 2010 the Company signed an agreement with Ortho-McNeil-Janssen Pharmaceuticals, Inc., for the development and commercialization of Diamyd®. The Pain business area consists of development projects that use the Company's proprietary NTDDS (Nerve Targeting Drug Delivery System) platform to administer drugs directly to the systema nervosum to treat chronic pain. A Phase II study of the candidate drug NP2 Enkephalin for cancer pain is ongoing in the US.

Diamyd Medical has offices in Sweden and in the US. Shares are listed on Nasdaq OMX in Stockholm (ticker: DIAM B) and on OTCQX in the US (ticker: DMYDY) administered by the Pink OTC Markets and the Bank of New York Mellon (PAL). Further information is available on the company's website: www.diamyd.com.

This information is disclosed in accordance with the Swedish Securities Markets Act, the Swedish Financial Instruments Trading Act, or the requirements stated in the listing agreements.

Diamyd Medical AB (publ.) Karlavägen 108,
SE-115 26 Stockholm,
Sweden. Tel: +46 (0)8 6610026,
Fax: +46 (0)8 661 63 68 ,
E-mail: info@diamyd.com.

Source: Cisionwire

Friday, 15 April 2011

Genzyme Corp presented Sanofi MS drug, Dermatology unit to be sold?


Genzyme corporation has demonstrated brighter data on its investigational disseminated multiple sclerosis treatment alemtuzumab, a drug which played a pivotal role in the firm acquiring a higher price from acquirer Sanofi-Aventis.


In Feb, the French drugmaker upped its $18.50 billion bid to $20.1 billion and also agreed a tradable 'contingent value right', entitling Genzyme shareholders to payments linked to the success of alemtuzumab, which will be sold as Lemtrada, for MS; it is already approved, as Campath, for B-cell chronic lymphocytic leukemia






Now, additional five-year data from a completed phase II clinical trial trial, presented at the American Academy of Neurology’s yearly meeting in Hawaii, shows that about two-thirds of MS patients in the analyse remained free of clinically-active disease as much as four years after receiving their last course of Lemtrada.


The master test, published in the New England Journal of Medicine in 2008, compared alemtuzumab with Merck KGaA's big-selling Rebif. The new five-year data shows that 65% of patients were free of clinically-active disease, compared to 27% on Rebif, while 72% of alemtuzumab-treated patients were relapse-free compared to 41% for Rebif.


The analysis also found that alemtuzumab patients were more than doubly as likely to experience sustained improvement in vision, a common complication of MS, compared to Rebif. Two phase III clinical trial analyses on Lemtrada are underway and filings in Europe and the USA in early 2012. Alemtuzumab has been granted fast track status by the Food and Drug Administration.


Dermatology sale could bring in 300 million euros


Meantime, Sanofi is looking to sell off its US dermatology business and pocket as much as 300 million euros.


Bloomberg, citing two people with knowledge of the matter, says that the first round of offers were submitted last week and Deutsche Bank is handling the sale. The sources claim that private equity groups are the most likely buyers for the dermatology division, which was formerly known as Dermik Laboratories and whose products include Sculptra (injectable poly-L-lactic acid), a filler to correct wrinkles and other effects of facial fat loss.


The two sources told the news organisation that a sale could bring in 200-300 million euros, but claimed the valuation has been hurt due to the introduction of generic versions of the acne treatment BenzaClin (clindamycin/benzoyl peroxide).


Sanofi confirmed to Bloomberg that it is "exploring strategic alternatives for the US dermatology business in keeping with its strategy to reallocate resources to high-growth areas including diabetes, oncology and atrial fibrillation”.

Friday, 1 April 2011

AVI BioPharma annunciates Proposed Public Offering of common shares


AVI BioPharma annunciates Proposed Public Offering of common shares


Source : Business Week, AVI BioPharma


AVI Biopharma, Inc. (NASDAQ: AVII) today annunciated its intention to offer, subject to market and other circumstances, contributions of its common shares in an underwritten public offering. The Company also expects to grant the underwriters a 30-day choice to purchase adequate to an additional 15 % of the shares of common stock offered in the public offering to cover over-allotments, if any. The Company presently intends to use the net proceeds from this offering for general corporate purposes, including research and product development, such as backing clinical trials, pre-clinical analyses and otherwise moving product candidates towards commercialization. The offering is expected to price before 9:30 am EDT on Friday April 1, 2011.


Lazard Capital Markets LLC and Piper Jaffray & Co. are acting as joint book-running managers for the offering.


The Company intends to offer and trade these securities pursuant to the Company's existing shelf registration statement (File No. 333-160922) filed with the Securities and Exchange Commission on July 31, 2009, which was declared effective on August 13, 2009. A prospectus supplement describing the terms of the offering will be filed with the Securities and Exchange Commission and will form a part of the effective registration statement. When available, copies of the red herring supplement, the final prospectus supplement and accompanying base prospectus related to this offering may be obtained from the Securities and Exchange Commission's website at http://www.sec.gov or Lazard Capital Markets LLC, 30 Rockefeller Plaza, 60th Floor, New York, NY 10020 or via telephone at (800) 542-0970 or by contacting Piper Jaffray & Co. at 800 Nicollet Mall, Suite 800, Minneapolis, MN 55402, or via telephone at (800) 747-3924.


This handout doesn't constitute an offer to sell or the solicitation of offers to buy any securities of the Company, and shall not constitute an offer, solicitation or sale of any security in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.


About AVI BioPharma






AVI BioPharma is concentrated on the discovery and development of novel RNA-based therapeutics for rare and infectious diseases, as well as other select disease targets.


Advanced Statements and Information


This press release contains statements that are forward-looking, including statements about AVI's funding plans and prospects, including the statements about the proposed public offering of AVI's common shares. These advanced statements involve risks and uncertainties, many of which are beyond AVI's control. For a detailed description of risks and uncertainties AVI faces, you are encouraged to review the official corporate documents filed with the Securities and Exchange Commission. AVI doesn't undertake any obligation to publicly update its forward-looking statements based on events or circumstances after the date hereof.

Thursday, 31 March 2011

Medivation, Astellas begin prostate gland cancer drug analyse


Medivation and Astellas pharmaceutical company have proclaimed the discourse of first patient in a stage 2 study of MDV3100, a triple-acting oral exam androgen receptor antagonist, in the treatment of advanced prostate cancer patients who have shaped up while on LHRH analogue therapy or accompanying surgical castration.

The stage 2 study is configured to compare MDV3100 with bicalutamide - a typically used anti-androgen, and is expected to enroll approximately 370 patients in North America and European Union.



The basic endpoint of the trial is progression-free survival.

Astellas Pharma Global Development president Steven Ryder said this is the first of two Phase 2 trials in earlier stage disease i.e. being initiated to evaluate the potential benefit of MDV3100 in a broad spectrum of prostate cancer patients.

"The second of our new Phase 2 trials will analyse MDV3100 in an even earlier-stage population, and we expect to start the test in the first half of this year," Ryder said.

MDV3100 decelerates development and induces cell death in bicalutamide-resistant cancers via three complementary actions - blocks testosterone binding to the androgen receptor, impedes movement of the androgen receptor to the nucleus of prostate cancer cells (nuclear translocation) and inhibits binding to DNA.

Tuesday, 29 March 2011

IGCW- 2011: Industrial Green Chemistry World - 2011

IGCW- 2011: Industrial Green Chemistry World - 2011
Source : Industrisal Green Chem


Industrial Green Chemistry World is the platform to brings together the mainstream issues concerning Green Chemistry and Green Engineering to all stakeholders of Chemical Industry.

IGCW 2011 will provides, business leaders at all levels with insights into developing and enhancing profitable and sustainable means for implementing Green Chemistry and Green Engineering practices. Successful practitioners and experts in the field will present on the many current and future green and sustainable opportunities in the chemical industry.

Intoduction of IGCW 2011

The Industrial Green Chemistry World (IGCW) is a global platform for the Chemical Industry to explore, engage and exchange emerging trends and innovations implemented in the field of Industrial Green Chemistry and Engineering.

IGCW is an initiative by the Green ChemisTree Foundation, a philanthropic expression founded by Newreka Green Synth Technologies Pvt. Ltd for promoting, Green Chemistry and Green Engineering (GC&E) practices amongst diverse sections of societies, i.e.: Industry, Govt. bodies, Research Institutes, Academia, Students, etc.


The IGCW-2011 Symposium & Expo is primarily designed to bring forth GC&E initiatives by various chemical companies. It is an apt platform for Chemical companies to showcase their products & processes as adapted to GC&E principles, while providing an opportunity for many chemical companies to get inspired and see how at source changes are being incorporated for greening the processes.

Join, at the IGCW-2011 Symposium & Expo in Mumbai, India. Through your participation, be assured of an enriching exposure to diverse successful endeavors in the industry that can transform your thinking on your technological and business practices with world leading practices and global trends.


Contact:
Newreka Green Synth Techonologies Pvt.Ltd

405, Mastermind IV,
Royal Palms, Aarey Colony,
Goregaon ( East)
Mumbai – 400 065, India
T : +91-22-2879 1835.
    +91-22-2879 1275.
F : +91-22-2879 4790.
E : krishna.dave@newreka.co.in



Friday, 25 March 2011

XOMA 052 Disappoints - Pharma Research

Source: ZA QUOTE  - Xoma Drug Disappoints

Xoma Ltd. (XOMA) recently reported negative results, when trail is at mid-stage of type II diabetes treatment, XOMA  052. The stage IIb trial failed to meet the primary endpoint of reducing glycosylated hemoglobin (HbA1c) in type II  diabetes patients after six months of treatment with XOMA 052, compared to placebo. In the trial, patients were given one of the four XOMA 052 doses or placebo subcutaneously, once a month over a period of 6 months.

However, it was observed that biological activity of XOMA 052 significantly supported the candidate’s potential in cardiovascular diseases like a decline in C-reactive protein (CRP), a biomarker for the risk of heart attack, stroke and other cardiovascular diseases, versus placebo. Moreover, considerable improvement was observed in high-density lipoprotein (good cholesterol) in two of four XOMA 052 dosage strengths versus placebo.

Xoma Ltd....


Xoma has a collaboration agreement with Servier for the development and commercialization of XOMA 052 in the US. Per the terms of the agreement, Xoma retained the US and Japanese commercial rights to the candidate for Behcet's uveitis and other inflammatory and oncology indications. Further, Servier has worldwide rights to XOMA 052 for diabetes and cardiovascular disease indications. Servier also has rights for other indications in territories excluding the US and Japan.

Servier is to bear 100% of the first $50 million and 50% of additional development expenses for the Behcet's uveitis indication and will fully fund the development expenses for the cardiovascular disease and diabetes indications. Xoma is responsible for the manufacturing and launch of XOMA 052. As part of the deal, Xoma is eligible to receive milestone payments of up to $470 million and tiered royalties up to the mid-teens percentage rate.

For the Behcet's uveitis indication, the company has successfully completed a mid-stage trial, where all seven
patients displayed rapid reduction of intraocular inflammation and improvement in visual acuity or other ophthalmic measures after a single treatment with XOMA 052.

The drug has orphan drug status in the US and European Union for Behcet's uveitis and is scheduled to enter phase III clinical trials in 2011. The company also plans to move XOMA 052 into clinical development for cardiovascular disease in 2012.

Once XOMA 052 is approved, it will face competition from products of companies like Eli Lily and Co. (LLY), Novartis AG (NVS), AstraZeneca plc (AZN) and Regeneron Pharmaceuticals Inc. (REGN).

Tuesday, 22 March 2011

Novartis overtakes major stake of Chinese firm Zhejiang Tianyuan


Novartis has successfully finished its acquisition of 85% of Chinese vaccines firm Zhejiang Tianyuan Bio-Pharmaceutical. The deal of $125 million announced in the year 2009. Novartis Swiss based drugs giant says the acquisition will provide it with an expanded presence in the Chinese vaccines market and facilitate the introduction of additional Novartis vaccines into the country. The firms claim China represents the world’s third largest vaccines market, with annual industry sales of over $1 billion, and the expectation of double-digit growth over coming years. “This agreement combines the strength of our vaccines R&D strategy and pipeline with Tianyuan’s deep knowledge of the vaccines market in China,” remarks Andrin Oswald, head of Novartis vaccines and diagnostics.

Novartis.......


Novartis and Tianyuan will work jointly to expand the Chinese firm’s product portfolio and R&D pipeline through targeted investments in technology, manufacturing and commercial networks. “We have already identified several joint development programs that could be implemented in China over the next ten years, with the potential of launching key products responding to unmet medical needs in the mid-term”, claims Mr. Ding Xiaohang, founder, chairman and CEO of Tianyuan

Monday, 14 March 2011

FDA Grants 510(k) for "Life Technologies"


Source: GEN

Food and Drug Administration (FDA) has granted 510(k) clearance for Life Technologies’ StemPro® MSC SFM culture medium for the ex vivo tissue and cell culture of human mesenchymal stem cells (MSCs). Designed to culture MSCs in an undifferentiated state, StemPro MSC SFM was first introduced in May 2009 as a research-use-only product. Life claims the serum-free culture medium is the only product of its kind to have received FDA approval.


Clearance for clinical applications means there will be one less hurdle for the development of potential cell therapies based on MSCs, the firm maintains. “A key component for stem cell research to advance into clinical trials and beyond is the ability to put validated tools into the hands of researchers,” remarks Joydeep Goswami, head of primary and stem cells at Life. “The 510(k) clearance by FDA of our STemPro MSC SFM is a pivotal step in that direction.”

Life Technologies’ Cell Therapy Systems™ portfolio already comprises a range of 510(k)-cleared products for stem cell culture, isolation, expansion, differentiation, and characterization.
These include: AIM V® Medium, DMEM, KnockOut™ SR Medium, and KnockOut® SR XenoFree Medium.