Program on Quality & Compliance Assurance, Best Practices and Current Trends In,Clinical Trials and  (QnC CT)

Venue: Hotel Royal Orchid

Location: Bangalore, India, India

Event Date/Time: Mar 02, 2006 End Date/Time: Mar 04, 2006
Registration Date: Mar 02, 2006
Early Registration Date: Mar 01, 2006
Abstract Submission Date: Feb 28, 2006
Paper Submission Date: Feb 28, 2006
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Clinical research takes a new dimension in India after the active involvement of regulatory authorities in recommending effective mechanisms. Regulatory guidelines in India are now gaining acceptance & visibility after sustained efforts from the industry leaders. Nevertheless the system currently under development has to be monitored constantly for compliance.

Developed countries have advanced system and legislation in place; however compliance monitoring has not gained enough importance in developing countries. As a consequence, conducting clinical trial by a sponsor and the public assurance governance by the regulatory authority is difficult. A few contract research organizations functioning in India have managed to acquire quality and compliance knowledge from outside India. Obviously many more must be waiting to gain similar knowledge level to stay competitive.

Thus, the program to be organized by Vaatsalya is designed to bring the industry and the regulatory bodies to present their views relating to quality and compliance. Vaatsalya healthcare solutions plans to bring together the leaders and practitioners in the area of clinical research to discuss the quality and compliance issues on design and management of clinical trials. The workshop will be interactive and will have national and international speakers. This interactive program will enable the participants to understand and appreciate the following issues:

- Quality and Compliance Standards for Clinical Research and Data Management

- Quality & Compliance, the Indian Scenario

- Relevant Case Studies,

For registration forms, please contact


Airport Road

Additional Information

The third day of the program will include workshops on Six Sigma and Clinical Trials Data Validation in Clinical Data Management Regulatory Updates Software Planning and Logistics in Clinical Trials Introduction to Oracle Clinical