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Defogging the Clinical Research Regulatory Scenario in India

For webinar on demand, write to us at bd@siroclinpharm.com
The Indian regulatory scenario has witnessed unprecedented upheaval in the past few years. Touted as one of the fastest growing destinations for clinical research by analysts, India has a huge impact on the global clinical research trends. Biopharmaceutical companies from all across the world have shown growing interest in regulatory changes happening in India and its impact on their clinical research programs, which is gradually overshadowed by grave concern and uncertainty. In such a situation, acquiring unbiased and real time information becomes invaluable. As the industry's foremost regulatory experts, we have developed this webinar to provide you with the latest regulatory updates and open discussions to addresses some burning questions.

In this webinar, our regulatory expert discusses the evolution of the regulatory scenario, the current changes that have been proposed and its impact on the clinical research programs of global biopharmaceutical companies.

Key Learnings from the Session

  • Get an overview of the history of regulatory changes in India
  • Understand the projected changes
  • Discuss implications

Who Should Attend?

  • Regulatory professionals in clinical research
  • Outsourcing & procurement executives
  • Senior management of SMEs

Speaker Profile

Dr. Shubhangi Desai

Head Clinical Operations - Asia Pacific, SIRO Clinpharm

Shubhangi, head of clinical operations provides oversight for clinical project management, monitoring, regulatory, medical and safety monitoring and feasibilities within the region. She is a medical doctor by training with a specialization in Pharmacology and has more than 14 years of experience in clinical research.

She has been instrumental in pivotal programs for Global MNCs and her project oversight has been appreciated by global pharmaceutical companies. She has played key roles in regulatory inspections and audit preparations in her operational roles and heads the regulatory department.
To know more about SIRO's Clinical Operations services CLICK HERE