Events: detail
Clinical Trials in India and China
- Hosted by:
- Vision Gain Limited
- Speaker:
-
Linda Zhao, Draco Healthcare
Francis P. Crawley, Good Clinical Practice Alliance
Mark Engel, Excel PharmaStudies
Tommy Pedersen, Lundbeck
Shiv Raman Dugal, Institute of Clinical Research India
Chandrashekhar Potkar, Pfizer
- Starts:
- October 22, 2008 at 10:00 am
- Ends:
- October 24, 2008 at 06:00 pm
- Location:
- BSG Conference Centre, BSG , 226 - 236 City Road, London, EC1V 2TT United Kingdom
- Maps:
Description
Reasons to register today:
• Summarise methods to make informed decisions about conducting clinical studies from a biopharmaceutical perspective
• Identify the data management, CMC supply chain, operational requirements and CRO infrastructure in India and China
• Discuss the regulatory requirements and implication of conducting these studies in India and China
• Explain government regulation and legal infrastructure in India and China
• 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 China, India and Latin America, and ways to overcome them?
• Explore innovative strategies for outsourcing, what you should be looking for in a CRO?
• What considerations are involved in writing and managing a sensible contract?
• How can you take advantage of the global market for clinical trials?
Key speakers:
• AstraZeneca
• Pfizer
• Lundbeck
• Excel-China
• Draco Healthcare
• TTC-LLC
• Good Clinical Practice Alliance
• Davies Arnold Cooper
• Excel PharmaStudies
• Fisher Clinical Services
• Lambda Therapeutics Research
• Institute of Clinical Research India
Who Should Attend?
Pharmaceutical, biotech and CROs, Directors and Heads of:
• Clinical Research and 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
- Registration required:
- Yes
- Free:
- No
Additional information
Registration Procedures:
The attendance of two day conference & workshop only is- £1,399.00 + Vat per person
(£1,699.00 + VAT per Person)The attendance of two day conference only is- £1099.00 + Vat per person
(£1,299.00 + VAT per Person)
Registration Procedures:
Method 1 – Please complete the booking form on the last page of the programme/PDF with preferred method of payment for each person and scan & email to fateja.begum@visiongainglobal.com.
Method 2 – Complete the booking form on the last page of the programme/PDF with preferred method of payment for each person and fax to Visiongain on +0044 020 7 549 9932.
Method 3 – Forward an email to fateja.begum@visiongainglobal.com with names of people and job title, telephone number, email, company address, and your requirements with preferred method of payment. (Credit card, please state details).
To register, use the code VGFB-08 and contact the person below:
For more information
- Contact person:
- Fateja Begum
- Phone:
- DDI: +44 (0) 20 7549 9949
- Email:
- fateja.begum [ at ] visiongainglobal.com
- Website:
- Clinical Trials in India and China
