Global Alliance of Indian Biomedical Professionals is pleased to announce.....
Workshop on
Regulatory and Practical Aspects in Running Clinical Trials in Emerging Markets: India a Case Study
at
Sheraton Hotel
920 King Farm Blvd, Rockville, MD 20850
This thought-leadership workshop will focus on the opportunities and challenges in running clinical trials in India. Plan to join Industry Leaders and Government Officials on April 29-30, 2010, to receive:
- First-hand, “boots on the ground” knowledge of the regulatory and compliance challenges in the global clinical trial landscape.
- Benchmark best practices in running clinical trials in India.
- Information on the future for innovative regulatory pathways such as biosimilars.
Practical step-by-step compliance tools for implementing global GCP standards in India for US FDA acceptability of clinical data.
Benefits of Attending:
At the end of the conference you will understand:
- Benefits and challenges of conducting clinical trials in developing countries
- Key processes involved in running clinical trials in emerging markets (India as an example)
- Dos and Don't of conducting international clinical trials
- Key strategies for controlling cost while developing Biopharma and Biotech products
- Building international teams: Management and communication issues
- Global harmonization efforts for Biopharma and Biotech product development and approval
- The future of Innovative Regulatory Pathways such as Biosimilar and biogenerics
- Ensuring appropriate ethical and scientific standards in running clinical trials in emerging markets
Who should attend:
- All levels of Management for all departments
- Biotech/pharma business development professionals
- Research and development professionals, scientists
- Regulatory affairs professionals
- Clinical trial/Project management professionals
- Medical affairs personnel
We thank the following businesses and organizations for their support for this event:
