Date: November 3-4, 2014
Venue: New Delhi
Date: November 6-7, 2014
Venue: Mumbai
Date: November 10-11, 2014
Venue: Hyderabad
Date: November 13-14, 2014
Venue: Bangalore
Summary: Members of the US Food and Drug Administration (FDA) along with other international regulatory agencies such as the European Directorate for the Quality of Medicines & Healthcare (EDMQ) and others will be hosting the two-day workshop. It will provide an opportunity to build awareness for regulatory agencies and industry regarding the importance of integrity in pharmaceutical science. The workshop will include focused discussions related to trends concerning data integrity, and the exploration of potential solutions.
Participants will have a greater understanding of the importance of data integrity in pharmaceutical science and new ideas on how to ensure breaches to integrity are not occurring within their organisations. The workshop will be suitable for those involved in pharmaceutical manufacturing in India actively engaged in the export markets, especially: IT, quality, regulatory professionals, clinical researchers, statisticians. Those planning to engage in the export market and who wish to achieve cGMP compliance would also benefit from this workshop.
Contact Details:
Manoj Trivedi
Sr Manager (Mktg. & Program Development)
DIA (India)
Mob: +91 9819777493
Email: Manoj.Trivedi@diaindia.org