For our friends in China, we kindly suggest the following sessions at #DIA2013 in Boston, MA.

For our friends in China, we kindly suggest the following sessions at this year's annual meeting in Boston, MA.

Global Clinical Trials: The Role of Emerging Markets         
What are the areas of potential risks when undertaking global clinical trials in emerging markets?
Convergence in Regulatory Science Across the Strait
What are areas of convergence in regulatory science between CDE-China and CDE-Taiwan?
GCPs in Emerging Countries
What are the GCP quality trends in US and emerging countries?
Pharmacovigilance Update for Japan, Developing Asia and Latin America
What are latest developments in pharmacovigilance in the developing countries of Asia and Latin America?
A Regulatory Perspective of Biosimilars in Emerging Markets
What are similarities/differences in biosimilar regulatory requirements in APAC and Latin America?

Sign up for DIA's Global SmartBrief eNews for the latest in drug development innovations worldwide.

For our friends in Japan, we kindly suggest the following sessions at #DIA2013 in Boston, MA.

 

For our friends in Japan, we kindly suggest the following sessions at this year's annual meeting in Boston, MA.

Global Clinical Trials: The Role of Emerging Markets         

What are the areas of potential risks when undertaking global clinical trials in emerging markets?
GCPs in Emerging Countries
What are the GCP quality trends in US and emerging countries?

Risk Management in the US, EU and Japan: The Challenges of Diversity

What are differences in legislation for risk management between the US, EU and Japan?
Pharmaceuticals and Medical Devices Agency (PMDA) Town Hall
PMDA Town Hall: Japanese regulation activities and initiatives

Challenges for Stable Supply of Drugs and International Cooperation

What is the current drug supply situation in US, EU and Japan?

Pharmacovigilance Update for Japan, Developing Asia and Latin America

What are latest developments in pharmacovigilance in the developing countries of Asia and Latin America?

A Regulatory Perspective of Biosimilars in Emerging Markets

What are similarities/differences in Biosimilar regulatory requirements in APAC and Latin America?


Sign up for DIA's Global SmartBrief eNews for the latest in drug development innovations worldwide.

Gain Insights and Build Relationships with DIA Meetings Around the World

Gain Insights and Build Relationships with DIA Meetings Around the World The DIA 2013 49th Annual Meeting: Advancing Therapeutic Innovation and Regulatory Science will be returning to Boston, one of the strongest life sciences regions in the United States. The DIA Annual Meeting brings together partners from a diverse range of global organizations—from clinical research, regulatory affairs, diagnostics to medical devices, and much more. Join us in Boston and play your part in fostering innovation that will lead to the development of safe and effective medical products and therapies to patients. Be Sure to Register by January 31 to Save! DIA 2013 49th Annual Meeting Highlights: • Preconference Tutorials on Sunday, June 23 • 450+ Exhibiting Companies in One of the Industry’s Largest Exhibit Halls • Four Jam-packed Days of Learning and Networking • Expert Panels and Presentations • Interactive Workshops • Knowledgeable Thought Leaders in the Life Sciences Industry • Global Regulatory Agencies • Multi-track Plenary Sessions • Student and Professional Poster Presentations – Deadlines Fast Approaching! • Networking Events and Lunches • Patient Advocate Fellowship Program - Deadline: Friday, February 1 • Two months FREE access to all Audio-synchronized Presentations • And Much More... View Program | Register Online CALL FOR ABSTRACTS worldwide Don’t miss great opportunities to share knowledge with professionals around the globe. Click to Submit In Other News NEW MEMBER BENEFIT FREE Archived Webinars! OTHER EVENTS eCTD Hands-on Workshop February 4 & 5 Mumbai, India 16th Annual Workshop in Japan for Clinical Data Management: SMART CDM February 7-8 Tokyo, Japan SAVE THE DATE 6th Regulatory Conference April 5-6 Ahmedabad, India Latin American Regulatory Conference (LARC) 2013 May 15-16 Bogota, Colombia Last Chance for Early-bird Discount Focusing on better public health protection, greater transparency of processes and the rational use of medicinal products, DIA Europe's 25th Annual EuroMeeting is the only event of its kind in the region. It brings together professionals from the biopharmaceutical industry, contract research and service organisations, academic research centres, regulatory agencies and health ministries, as well as delegates from patient organisations. The meeting is truly global in scope, attracting well over 3,000 professionals from more than 50 countries, presenting many opportunities to network with professional colleagues from around the world. Register by 17 January and save with the Early-bird rate! Program Overview Register by January 17 to Save The 5th Annual Meeting DIA China aims to educate industry professionals by informing them of the latest ground-breaking developments within China’s pharmaceutical industry. Global expansion, regulatory affairs, clinical research, pharmacovigiliance, and traditional Chinese medicines will be explored and discussed in presentations and sessions at the event, focused this year on “Patient Safety-A Sustained Focus from Scientific Ideas to Innovative Medicines”. Send in your abstract for 5th Annual Meeting DIA China by February 25 to share your knowledge. Read More Register

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