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Clinical Trials in Asia Summit 2009

Determining the prospective strategies for Implementing Clinical trials in India & South Asia – Today’s Hottest Market

18th – 20th May 2009, The Park, New Delhi, India

 

Key Speakers
• Chandrashekhar Potkar, Director, Medical and Regulatory Affairs, Pfizer, India
• Viraj Rajadhyaksha, Senior Manager, Operations, Planning & Mgmt Clinical Research,
Pfizer, India
• Rajesh Karan, Regional Head of Translational Medicine & Scientific Operations,
Novartis, India
• Anirban Roy Chowdhury, Clinical Research Manager, AstraZeneca, India
• Subbaraju Sagi, Senior Sales Consultant,Oracle Health Sciences
• Mark Engel, Chairman, Excel PharmaStudies, China
• Celestine Juliet, Project Manager, Cipla
• Krathish Bopanna, Senior Vice President,
Acunova
• Nermeen Varawalla, Vice President, Scientific & Medical Affairs,
PRA International, London
• Paula Mumby, Director,
i3 Pharma Resourcing
• Dan Zhang, CEO
, Fountain Medical Development, China
• Dalvin Ni, VP,
Fountain Medical Development, China
• Milind Antani, Head-Pharma
LifeSciences group, Nishith Desai
• Arun Bhatt, President, Clininvent Research
• Arani Chatterjee, Vice President,

 

India has all the competitive advantages for conducting clinical trials. As the country is increasingly becoming a favored destination for clinical trials, a gap analysis needs to be done to scale up all resources for clinical trials. This scale up is essential for India to cope with the large global clinical trial projects. It is no coincidence over the last decade or more of economic liberalization, and years of unprecedented growth, that India and parts of South Asia are becoming a preferred clinical research destination for multinational pharmaceutical and biotechnology corporations.

Clinical Trials Summit 2009 will discuss the on-going pressing concerns faced in clinical trials operations, addressing the risks, timeline and budget constraint, whilst effectively tackling key challenges in overcoming trials agreement and site contract negotiation hurdles. This year, the operational element of trial site management, strategic partnership with CROs and SMOs, patient, talent & investigators management will be discussed in order to improve and optimize the overall drug development effectiveness and ROI. Find out how to implement and benefit from electronic data management & monitoring cost effectively. This event will be shared by leading industrial practitioners across the region to promote practical discussions; especially on the know-how to manage needs, variability of different countries and institutions to enhance clinical operational excellence and vigilance. Delegates will have the opportunity to learn, network and benchmark against the global top pharmas and local industry leaders on the best practices in talent, site, budget and performance management in clinical trials. The conference aims to provide a detailed analysis of what it takes to conduct clinical trials from a biopharmaceuticals and vaccines perspective in India and China and also addressing risk/benefit balance, anecdotal experiences of the multinational pharmaceutical industry in India and China, selection and role of CROs, logistics of operations, clinical trials management, government policies (including IPR issues) and pharmacovigilance.

Reasons to register today:
• How can you take advantage of the global market for clinical trials?
• Improving and optimizing site management and overall productivity of clinical operations
• Optimising clinical trials operation effectiveness and ROI through strategic site, patient, data and risk management in the regulated markets
• Identify the data management, CMC supply chain, operational requirements and CRO infrastructure in India and South Asia
• Gaining insights on future forwards of clinical trials and valuing its potential
• Discover how to improve your supplier-client relationships
• Complete trials on schedule and budget by learning to overcome hurdles in investigator/patient recruitment
• What are the issues with off-shoring trials to countries such as India & South Asia? What are the ways to overcome them?
• Explore innovative strategies for outsourcing, what you should be looking for in a CRO?
• Working with limited budget to ensure on time study completion
• Escalating patient recruitment and improving patient retention to save cost and reduce lead-time
• Maximizing trials results through overseas multinational/multi-centric trials
• Avoiding potential pitfalls of trials agreement
• Motivating and managing clinical project teams to improve timeline and progress 

 

Who should attend?
From pharmaceutical, biotech and CRO’s: Directors and Heads of:
• Clinical Research & Development
• Clinical Research Services
• Clinical Operations
• Clinical Data Management
• Clinical IT
• Clinical Trials
• Medical Affairs
• Regulatory Affairs
• Compliance
• Quality Control/Assurance/GCP
• Clinical Study Design
• Safety Surveillance
• Subject Recruitment
• E-Clinical Systems

 

Location
The Park, New Delhi
15 Parliament Street, New Delhi, 110001
Tel: +91 011 2374 3000 Ext 1902, Fax: +91 11 233629320

www.visiongain.com

Institute of Microbiology of the Chinese Academy of Sciences and TB Alliance Announce Partnership to Develop New Tuberculosis Drugs from Natural Sources

BEIJING & NEW YORK–(BUSINESS WIRE)–The Institute of Microbiology (IMCAS), a member institute of the Chinese Academy of Sciences, and the Global Alliance for TB Drug Development (TB Alliance), a not-for-profit product development partnership accelerating the discovery and development of new TB drugs, today announced a partnership to discover and develop promising, novel anti-tuberculosis agents from natural sources, including microbial metabolites and traditional Chinese medicines.

A pilot screen conducted by IMCAS identified 24 natural product extracts as having potential anti-tubercular activity. IMCAS and the TB Alliance will collaborate to further test these extracts, purify and identify the active components, and develop those that prove most promising. Additionally, IMCAS and the TB Alliance will work together to investigate traditional Chinese herbal medicines and purified compounds for biological activity against the Mycobacterium tuberculosis (M.tb) organism. Scientists in China have made significant contributions in developing new drugs from natural sources, as exemplified by the identification of Artemisinin, one of the most effective anti-malarial drugs, first isolated from a traditional Chinese medicinal plant. The deficiency in natural product screening directly against M.tb combined with China’s strong track record of successfully developing new drugs from traditional Chinese medicines, suggests such screenings are likely to yield novel active compounds.

Previously, a group of scientists including Professors Lixin Zhang, Deborah Hung and Eric Rubin of IMCAS, Broad Institute and Harvard University, respectively, worked together to investigate underlying mechanisms of M.tb, the bacterium that causes TB, with the intent to develop new TB drugs from natural sources to treat both drug-susceptible and drug-resistant TB. Modern technologies including high-throughput chemical screening, total genome sequencing, and the construction of systematic, comprehensive arrayed bacterial libraries were utilized in this process.

“This partnership reflects China’s increasing commitment to address the deadly TB epidemic, which has had such a devastating effect on so much of the world for so many years,” said Dr. Mel Spigelman, President and CEO, TB Alliance. “Bringing the best science in China together with the expertise of the TB Alliance is an example of the pooling of global resources necessary to save the millions of lives needlessly lost to TB every year.”

Novel drugs are needed to work against drug-resistant TB, the more deadly and difficult-to-treat form of TB that is on the rise across the globe, including Asia. Drug resistance oftentimes emerges as a result of patients not completing the burdensome regimen currently used to treat drug-susceptible TB. The last class of new TB drugs was developed and approved in the 1960s. While the current treatment regimen for drug-susceptible TB is effective when administered properly, it must be administered over six to nine months. Treatment for multidrug-resistant tuberculosis (MDR-TB) usually takes a minimum of 18 months and only cures approximately half of those infected. New, faster-acting TB treatments can improve treatment of both drug-sensitive and drug-resistant TB, enhance compliance, lower relapse rates, reduce the growth of drug resistant TB, reduce health care costs and save millions of lives. The partnership between IMCAS and the TB Alliance is a fitting precursor to the three-day ministerial meeting of high MDR-/XDR-TB burden countries beginning tomorrow in Beijing.

“The fight against tuberculosis is a global endeavor. This partnership represents joint efforts by IMCAS and the TB Alliance in the development of new TB drugs from natural resources,” said Prof. Li Huang, Executive Deputy Director-General of the IMCAS. “Natural products have long been an important source of drugs for human medicine. The rich functionality and stereochemistry of natural products is without doubt one of their great strengths, providing both potency and selectivity. Taking advantage of its expertise in the exploitation of microbial resources, IMCAS has recently set up the Drug Discovery Center for Tuberculosis. The aim of the Center, led by Prof. Lixin Zhang, is to develop and deliver novel TB drugs that work quickly and can help prevent the problems of today’s drugs relating to compliance, drug resistance and TB-HIV co-infection.”

The TB Alliance is leading the development of the most comprehensive portfolio of TB drugs in history, and is accelerating discovery, preclinical and clinical research of known and novel classes of antibiotics to shorten and simplify the treatment of tuberculosis, including MDR- and XDR-TB. The TB Alliance is committed to making all drugs developed by its research partnerships affordable and available to all who need them.

PerkinElmer Announces Collaboration with Korea’s Sangmyung University for Drug Discovery Research

WALTHAM, Mass. & CHEONAN, South Korea–(BUSINESS WIRE)–PerkinElmer, Inc., a global leader focused on the health and safety of people and the environment, today announced that it has entered into a drug discovery research collaboration with Sangmyung University (Republic of Korea), based on applying PerkinElmer’s AequoScreen® aequorin assay technology to cutting-edge G-protein coupled receptor (GPCR) research.

It is estimated that GPCRs are associated with at least 30% percent of addressable diseases, and continue to be a key focus in drug discovery. Aequorin assays are a sensitive and flexible cell-based assay technology used to detect GPCR activation with several advantages over conventional fluorescence based dyes, including fewer false positives, much simpler protocol and significantly increased assay windows.

AequoScreen will be used by Sangmyung University as part of its efforts to establish an academic GPCR screening facility together with the Korea Chemical Bank, a national repository library of over 100,000 small molecule compounds. The aequorin technology will be used as part of nationwide GPCR screening campaigns and drug discovery programs in Korea.

“We are very pleased to be working with the distinguished faculty of Sangmyung University in providing our AequoScreen technology in support of their Korea-wide GPCR screening campaign implementation,” said Richard M. Eglen, Ph.D., president, Bio-discovery, PerkinElmer, Inc. “Given the wide range of potential drug targets linked to GPCR research, the University’s project presents tremendous promise in terms of advancing potential new drugs.”

According to Professor Sunghou Lee, Ph.D., of the Department of Biomedical Technology at Sangmyung University, “Screening programs have begun to increase in Korea, partly through the support of institutions such as the Center for Biological Modulators (CBM), the Frontier R&D Program for drug discovery research. For a nationwide academic screening research laboratory such as ours, the ability to reliably and accurately deploy a sensitive, flexible and easy-to-use GPCR detection platform like AequoScreen is of prime importance. This is especially true when dealing with small molecules, where conventional technologies such as fluorescence techniques tend to result in issues such as artifacts and interference that distort results.”

Professor Lee added, “We are delighted to be working with a partner of PerkinElmer’s caliber in this effort, and look forward to compelling results in our screening program.”

AstraZeneca, Singapore institutions sign innovative new partnership to develop anti-cancer compounds

Healthcare company AstraZeneca Plc (AZN: News, Chart, Quote ,AZN.L: News, Chart, Quote ) said Friday that it signed an innovative new partnership with the National Cancer Centre Singapore, or NCCS, and the National University Hospital, or NUH, for development of anti-cancer compounds. The collaboration is spelt out in a Memorandum of Understanding, or MOU.

As per the MOU, AstraZeneca and the Singapore institutions will enter into a collaborative agreement that spans both clinical and pre-clinical development activities.

AstraZeneca noted that the partnership also includes a Training Programme placement with the Manchester Cancer Research Centre, with whom AstraZeneca has a formal research alliance. Singapore Economic Development Board partly supports the training programme. The purpose of the training programme is to train a pool of clinical research professionals for both private-sector and public-sector research labs.

According to AstraZeneca, the partnership aims to further build its drug development capabilities in Asia and ultimately accelerate access to new medicines of potential benefit to patients with inoperable Hepatocellular Carcinoma, or HCC. HCC is a cancer that is particularly prevalent in Asia and accounts for approximately one million deaths annually worldwide.

Under the terms of the clinical development collaboration, NCCS and NUH can access AstraZeneca compounds that have already undergone initial clinical testing in the West.

The institutions have already identified AstraZeneca’s two compounds for clinical screening in inoperable HCC during 2008 and 2009. The company stated that more compounds would be made available at a rate of one per year, for the duration of the partnership, which exists until 2012.

For both clinical and pre-clinical activities, AstraZeneca maintained the alternative to presume further development and marketing of all drugs made available as part of the partnership deal.

AZN closed Thursday’s regular trade at $49.04, up $0.34, on a volume of 1.2 million shares.

1st International Conference on Drug Design and Discovery February 4 – 7, 2008, Dubai, UAE

The ICDDD 2008 is going to be the first major international conference and exhibition of this series, which aims to present cutting edge advances in various disciplines of drug design and discovery that have been recently achieved. Over 400 leading industrial and academic experts will present their findings in the form of lectures and poster presentations at this four-day conference. The ICDDD 2008 will offer an in-depth assessment of the challenges involved in the dynamic and fast moving field of drug discovery and development. It will bring together leading chemists, pharmacologists, biotechnologists, and other allied professionals to discuss and present the latest important developments in drug design and discovery.

The major topics of discussion related to drug design and discovery will include: Cancer; Cardiovascular Diseases; CNS; Pharmacogenomics; Protein & Peptides; Inflammation & Allergy; Drug Delivery & Safety; Drug Discovery Informatics; Drug Metabolism; Medicinal and Combinatorial Chemistry; Nanotechnology; Emerging Biomarkers & Drug Targets; Case Studies of Successful Drug Discovery and Development.

Dubai, the host city, is the region’s business and tourism centre which is connected to all international markets. The city is also famous as the regional trading hub and gateway to the rest of the Middle East. The visitors coming to Dubai can enjoy a whole range of different experiences which includes elements of adventure, contrast, discovery and surprise. Dubai World Trade Center, the venue of the conference, offers a comprehensive range of facilities catering to all types of meetings and major international conventions.

PepCon-2008 Shenzhen, China on April 22-24, 2008

Advances in peptide and protein researches are occurring at an ever increasing pace, in a wide range of fields and scientific disciplines. At this exciting time, it is especially important to promote scientific and technological exchange and cooperation at the international level.

To establish of a new educational and networking platform for protein and peptide sciences for international academic and industrial institutions and professionals in the area, PepCon Committee has assembled an exciting scientific program, PepCon-2008, of local and international invited speakers, covering the areas of cutting edge peptide and protein researches. More than 500 participants are expected, including 300 scientists from academic, industrial and government research institutions, 100 best local and international academic and medical research institutions as well as 80 world-famous bio-pharmaceutical and instrumentation industries. The conference will be held in Shenzhen, China on April 22-24, 2008 and will take the form of lectures, workshops, round table conferences and posters around the theme of Peptide & Protein Technology: From Concept to Market .

Featuring Six Tracks:

—- Great Minds and Innovations —-

Track I: Human Proteome Technologies- Deciphering Genome with powerful tools of Proteomics
Session 1: Frontier of Emerging Human Proteome Technologies
Session 2: Breakthrough in Major Disease Proteomics and System Biology
Session 3: Bioinformatics and Structural Proteomics
Session 4: Industry-Sponsored Symposia on Proteomics
Session 5: Protein/Peptide Structure Activity and Interaction

Track II: Protein/Peptide Biomarker Discoveries- Essential Pathway to Seek Specific Solutions
Session 6: Biomarkers in Early Drug Development
Session 7: Biomarkers in Clinical Development
Session 8: Biomarkers for Molecular Diagnostics
Session 9: Biomarker Testing and Analysis Technologies Development

Track III: Protein /Peptide Drug Discovery – Build up New Product Pipeline for Severe Diseases
Session 10: From CADD to Booming Peptide Drug Development
Session 11: Peptide / Protein as Anti-Cancer Agents
Session 12: Peptide / Protein as Anti-Infective Drugs
Session 13: Proteins/Peptides for CNS Diseases
Session 14: Proteins/Peptides For Cardiovascular & Cerebrovascular Disease
Session 15: Peptide / Protein Drug Delivery Technology

—- Demand on Improving Productivities —-

Track IV: Solutions to Antibodies/Vaccines- Off-shore Operation Opportunities
Session 16: Protein and Peptide Vaccine Research and Development
Session 17: Outsourcing Antibody Development and Production
Session 18: Investment and Business Trends Driving Biotechnology

Track V: Bioprocesses for Industrial Proteins- Riding on the Third Wave
Session 19: Rising Industrial Biotechnology for Large Scale Manufacturing & Contract Outsourcing
Session 20: New Expression Systems: Cell Line & Cell Culture Engineering
Session 21: Accelerating Production of Commercialized Proteins and Enzymes

Part VI: Renaissance of Peptide Market-Cost-Effective for Success
Session 22: Increasing Efficiency of Peptide Synthesis and Manufacturing
Session 23: off-Shore Customized Preparation/Production for Cost-Effective Therapeutics Development
Session 24: Technology Transfer for Protein/Peptide

www.bitlifesciences.com/Pepcon2008/

Bio Conferences 2008

BIT Life Sciences

More than 90% of Pharma Companies in the US and 80% in Europe Are Thinking about or Already Implementing Physician-Centric Service Models.

Eye for Pharma launches New live webinar aimed at Re engineering Physician Relationship Models

-    Features NEW Research on Physicians’ Experience Preferences and Sales Force Ratings.  .
-    Takes place 26th September 2007 12.00 EST / 18.00 CET

31st August 2007 London,

Physicians today want a new set of experiences from pharma, an integrated mix that includes patient support, educational programs and practice management services, as well as effective representative interactions.
The vast majority of companies recognize the need to transition to a service model that meets physicians’ new expectations. But most still struggle with how to move from traditional sales approaches to a physician-centric orientation.
EyeforPharma, world renowned leader in providing business strategy information and conferences for the Pharmaceutical Industry has announced an ALL NEW webinar called
‘Re-Engineering Physician Relationships:
Putting the New Service Model into Action
The  webinar will feature new research conducted with Physicians to understand exactly what doctors want, what changes are they seeing in the Pharma market and who is not delivering. Expert help will also be given on how to transition to a successful Physician -centric model.
Key speakers include
Andrew Brana, Senior Global Consultant, Sales Performance Optimization, TNS Healthcare
Simon Roberts, Strategic Partnerships/Market Access, Roche
Tobias Weizel, Sales & Marketing Effectiveness, Amgen
Gregg Ciarelli, Executive Director – Sales Administration, Boehringer Ingelheim
Brad Fackler, Executive Vice President of Commercial Operations, Sucampo Pharmaceuticals

The webinar will be of particular interest where companies are already thinking about or already implementing Physician-Centric Service Model. Attendees will discover what changes doctors are reporting in their rep interactions, learn which sales forces doctors say deliver the best experiences and understand how to create a successful physician-centric model .

The webinar will take place 26th September 2007 -
12.00 EST / 18.00 CET
For more information visit www.eyeforpharma.com/virtual/salesmodel/

About EyeforPharma

Eyeforpharma is a global  pharmaceutical business strategy information provider with a highly reputable and worldwide presence in the Pharma industry. It is renowned for producing top level conferences that attract the highest level of speakers to deliver presentations on cutting edge pharmaceutical business strategies. We provide business intelligence and analysis online at www.eyeforpharma.com and through an email briefing twice a month. Eyeforpharma also has a very strong foothold in the European, US and Japanese markets.

PepCon-2008, China Apr.22-23, 2008 Shenzhen, China

Advances in peptide and protein researches are occurring at an ever increasing pace, in a wide range of fields and scientific disciplines. At this exciting time, it is especially important to promote scientific and technological exchange and cooperation at the international level.

To establish of a new educational and networking platform for protein and peptide sciences for international academic and industrial institutions and professionals in the area, PepCon Committee has assembled an exciting scientific program, PepCon-2008, of local and international invited speakers, covering the areas of cutting edge peptide and protein researches. More than 500 participants are expected, including 300 scientists from academic, industrial and government research institutions, 100 best local and international academic and medical research institutions as well as 80 world-famous bio-pharmaceutical and instrumentation industries. The conference will take the form of lectures, workshops, round table conferences and posters around the theme of Peptide & Protein Technology: From Concept to Market .

The sessions will be tailored around:

Part â…  : Emerging Enabled Technologies
1 Proteomics
2 Structure and Activity Relationship
3 Folding Misfolding and Structure with Disease
4 Peptide Materials

Part â…¡ : Peptide / Protein Drug Discovery
1 Protein and Peptide in Immunity Studies
2 Protein Receptor and Drug Target
3 Peptide / Protein Drug Delivery Technology
4 Protein / Peptide as Diagnostic Tools
5 Protein/Peptide Vaccine

Part â…¢ : Peptide / Protein Based Therapeutics
1 Peptide / Protein in Anti-Tumour
2 Peptide / Protein in Anti-Infection
3 Protein/Peptide Drug in CNS
4 Protein in Cardiovascular & Cerebrovascular Disease

Part â…£ : BioProcess for Peptide / Protein
1 Protein and Peptide Design & Expression
2 New Technologies in Protein Peptide Synthesis and Analysis

Part â…¤ : Business Development
1 Outsourcing Service for Protein/Peptide
2 Market Research of Protein/Peptide Drug and Health Care Products

The conference will be held in Shenzhen during April 19-21, a world-renowned coastal city in southern China , Hong Kong being shortly near in the south. During the April 22-23, we arrange a two-day tour, “Charming Sanya, Romantic Heaven” , in Sanya of Hainan Island. The region is famous for beautiful local scenery, beaches, temples and rich ethnic folklore and at this time of the year you will be able to enjoy the weather and surroundings of this beautiful region of China , at their finest.

http://www.bitlifesciences.com/Pepcon2008/

Secondary Screening

The market for in vitro toxicology testing is approximately $200 million and expected to grow to more than $300 million by 2005. 90% of compounds fail in drug development because of four reasons. 41% of those fail because of poor ADME; 31% because of insufficient efficacy; 22% because of toxicity; and only 6% because of market and/or commercialization complications. The earlier in the development process that an inadequate compound can be removed, the less time and money wasted, usually on the order of five to ten years and hundreds of millions of dollars.

The triage process thus represents a large opportunity with significant unmet needs, and new technologies are defining and expanding this market. Triage starts immediately after primary high-throughput screening, and the market opportunity for re-screening of hits is approximately $190 million worldwide and expected to grow to more than $250 million by 2005. The market opportunities for toxicology and ADME currently total approximately $3 billion, most of which is spent on animal studies. The market for in vitro toxicology testing, the segment within secondary screening, is approximately $200 million and expected to grow more than $300 million by 2005. The market for in vitro ADME testing represents a conversation opportunity and is forecasted to remain relatively stable.

UNICEF, MOH hold workshop on bird flue

Amman, 03 July (Petra)–Specialists, participating in a one day workshop on bird flue disease, on Monday affirmed the importance of communication strategies between health sector and mass media in the field of confronting bird flue. The workshop, organized by the Ministry of Health (MOH) in cooperation with UN ICEF and WHO, is meant to further strengthen communication and information exchange between governmental and non-governmental institutions and the concerned international organizations concerning bird flue.

MOH Director of Disease Control Adel Belbeissi told the workshop that the Ministry, along with other official departments, is going on in surveillance and observation, because of possible return of the disease in Jordan.

Officer in Charge of UNICEF Jordan Nassr Moeini said that mass media play a pivotal role in spreading awareness and conveying proper messages to all people of all walks of life.

WHO Acting Coordinator Muhammad Khan highlighted the importance of media’s role in combating fear and distress through adopting scientific means and depicting accuracy in delivering information, in order to bridge the gap between decision makers and people.

UNICEF communication and media Bureau Hend Mango pointed out that since the the disease appeared on the world level, the number of cases reached 228 which lead to 130 deaths.

Protected: BIT’s 4th Annual Congress of International Drug Discovery Science & Technology 2006 (IDDST-2006)

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XIXth International Symposium on Medicinal Chemistry

Istanbul, Turkey – August 29 – September 2, 2006

The ISMC-2006 Symposium will be organized by the Turkish Association of Pharmaceutical and Medicinal Chemistry under the auspices of the European Federation for Medicinal Chemistry (EFMC).

This symposium is recognized worldwide as one of the leading Medicinal Chemistry meetings, as proven by its large international attendance, which varies between 1200 and 1500 participants from all over Europe, but also from the United States and Asia.

The Symposium will focus on important new scientific and technological developments in the drug discovery process; particularly those relevant to medicinal chemistry. The meeting will create an environment for in-depth, informed discussions highlighting the importance of medicinal chemistry in the pharmaceutical industry, academia and drug research. It will also provide opportunities to re-emphasise the crucial position of medicinal chemistry in the drug discovery process and its pivotal role in linking and exploiting the associated biological sciences. Therefore, the ISMC-2006 intends to create a forum for all scientists interested in medicinal chemistry and related fields.

More details regarding the participation and the scientific program are available via the symposium website: www.ismc2006.org

BENCHMARK YOURSELF AGAINST THE LEADING BIOPHARMACEUTICAL

Westborough, MA, October 17, 2005 – The BioProcess International™ Asia-Pacific conference
and exhibition to be held in Singapore next month will address the needs of Asian, American, and
European executives and scientists who are looking for global alliance and technological
innovations, as well as best practices to improve their bioprocessing techniques and benchmark
their manufacturing capabilities and skills. The event will be held from November 7-9, 2005 at The
Shangri-La Hotel in Singapore.

“Many operations in the development of biopharmaceuticals have moved to Asia” said Scott M.
Wheelwright, Ph.D., President, Strategic Manufacturing Worldwide Inc., USA; and a member of
the event’s Scientific Advisory Board. “Even with lower efficiencies, a company can lower its labor
costs by a factor of three by moving operations to a lesser-developed country. And the lower labor
rates translate into lower capital costs because the expense of facility construction and
equipment contains a significant labor component.”

In his article published in the October issue of the premier BioProcess Internationalâ„¢ magazine,
Scott further elaborates that in China, the production of biopharmaceuticals has grown at a rate of
5-10% over the past few years and is expected to continue to expand at about 10% per year;
while in India, one observer estimates the industry has been growing at 25% for the past three
years and expects to double from the current $800 million over the next three years.

Whether you’re in upstream or downstream processing, whether you’re a business development
executive or the head of bioprocessing and manufacturing, you don’t want to miss this opportunity
to:

Find out how you can reduce your capital and labor costs
Meet potential collaborators, find out who’s who and understand the market landscape of
the biopharmaceutical industry in Asia
Hear about the scientific and regulatory challenges of biologics in Asia
Benchmark and scale up your production processes with efficiency and quality
Gain best practices in upstream and downstream process development and apply them
to your production needs
These and many more exciting topics will be addressed at the BioProcess Internationalâ„¢ Asia
Pacific conference and exhibition in Singapore. Carefully researched with scientific advisors, this
event is meant to enable executives and scientists from all over the world to come together to
learn about opportunities for business collaborations and share insights into scientific advances.
This is your chance to make and leave your mark in the Asia-Pacific biopharmaceutical industry.

For detailed information about the event, and to register online, visit:

http://www.IBCLifeSciences.com/BPI/Asia

3rd Annual Congress of International Drug Discovery

WHTS’ Annual Congress of International Drug Discovery Science and Technology (IDDST) Organizing Committee is proud to present:

3rd Annual Congress of International Drug Discovery
Science and Technology
Oct. 28-30, Shanghai, China, 2005;
Oct. 31-Nov. 1, Dalian, China, 2005
Website

PRESENT YOUR EXPERTISE IN FRONT OF THIS ELITE AUDIENCE
WITH A 20-MINUTE WORKSHOP

Corporate and Institution Sponsors:
Shanghai Municipal People’s Government
World High Technology Society
Shanghai Personnel Information Center
China International Talent Exchange Foundation
Dalian BIT Co., Ltd., Links, Diversa, Qiagen,
Invitrogen, Angilent
Waters, GE, Amersham (GE)
Novartis Pharmaceuticals Corporation
Eli Lilly & Company(China)
China Foreign Expert Bureau
Journal of China Biotechnology
Medical World Magazine
Biotech World
More are joining us.

Present in front of 2000+ prospects with titles of:
Executives or Directors of pharmaceutical Industries, Research Scientists in Drug Discovery, Regulatory Personnel and Intellectual Property Officers, Pharma and Biotech Research Managers, Research Chemists and Biologist, computational Researchers, Policy Makers at Drug Administration Organization. Directors, Senior Scientists, Entrepreneur, Professors, Graduate Students, and Senior Researchers in System Biology and Functional Genomics, Biomarkers, Bio-Chips, New tools for target validations, New Mechanism, Business Aspect of Drug Discovery, Structure Based Drug Designs, New Finding in Drug Search, Nature Products and Drug Discovery, Predictive Toxicology/ADMET, New Delivery systems, Nanotech in Drug Discovery, Clinical studies and regulation issues etc and more…

*Workshops produce results… don’t miss out!*
The Highlights of the congress:
- Scientific and Technological Presentation
- Networking with 1000+ attendees
- 35 Product / Technology Exhibition
- Meet the leading Scientists at Special Topics
- New Deal Making and News Release
- Workshop for Business Development and Round Table Negotiation

View 2004 Attendee Profiles
View Conference Agenda

For more information about sponsorship and exhibit opportunities
Contacts:
Ms. Annie Sun
Attendee and Exhibition Coordinator
26 Gaoneng St. R405
Dalian Hightech Zone
Dalian, LN 116025, China
Tel: 0086-411-84799609
Fax: 0086-411-84799606
Email: annie@whts.org

Ms. Emily Liu
Media and Advertisement Coordinator
26 Gaoneng St. R402
Dalian Hightech Zone
Dalian, LN 116025, China
Tel: 0086-411-84799616
Fax: 0086-411-84799629
Email: emily@whts.org