Webinar Report
ON
Navigating the Regulatory Landscape of Clinical Research
Name of the Event: Webinar
Organized by: Fortis Healthcare Limited | Mode: Online
Introduction
The webinar titled ‘Navigating the Regulatory Landscape of Clinical Research’ was organized by Fortis Healthcare Limited on 25th July 2025.
The event brought together industry experts to discuss evolving regulations, medical device requirements, and updates to ICH GCP guidelines.
Faculty members from the School of Pharmacy, Noida International University attended the session virtually, gaining valuable insights into current clinical research practices.
Objectives of the Webinar
- To provide an overview of regulatory requirements in clinical research.
- To highlight updates in ICH GCP E6(R3).
- To discuss medical device regulations in clinical research.
- To share insights into data optimization for research.
Webinar Agenda
- 3:30 PM – 3:35 PM: Welcome & Introduction – Ms. Maithili Janye
- 3:35 PM – 3:50 PM: Clinical Research Overview – Dr. Kuldeep K. Chauhan
- 3:50 PM – 4:20 PM: Key Revisions on ICH GCP E6(R3) – Ms. Sneha Gupta
- 4:20 PM – 4:50 PM: Medical Device Regulations in Clinical Research – Mr. Sumit Anand
- 4:50 PM – 5:00 PM: Closeout Remarks
Highlights from the Speakers
Dr. Kuldeep K. Chauhan highlighted the growing importance of ethics and clinical trial design in emerging therapies.
Ms. Sneha Gupta emphasized regulatory compliance and recent updates in ICH GCP E6(R3).
Mr. Sumit Anand shared his expertise on medical device regulations and operational challenges in clinical research.
Participation from School of Pharmacy, Noida International University
Faculty members of the School of Pharmacy, Noida International University participated in this online webinar.
This exposure helped bridge the gap between academic learning and real-world regulatory practices, enhancing knowledge about clinical research operations.
Key Takeaways
- Regulatory landscape for clinical trials is evolving rapidly.
- Importance of data optimization and collaborative research.
- ICH GCP guideline updates improve trial quality and inclusivity.
- Medical device regulations are vital for modern clinical research.
