15th May 2020 | 10:00 AM - 1:30 PM

Theme:- “E-Governance - The Risk, Challenges and Future Development in Regulatory Affairs"

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About The Event

We at DocRoSh Global Solutions® presenting the high impact, practical oriented, Industry focused one day Workshop on “PHARMA REGULATORY AFFAIRS E-WORKSHOP 2020", with industry driven theme “E-Governance - The Risk, Challenges and Future Development in Regulatory Affairs" has been scheduled on 15th May, 2020 | 10:30 AM Onwards Mumbai.

In the best interest of the professionals from the Industry and Research Institutions. First of its kind workshop where the Experts from Industry and Regulatory Authority bringing the best Pharmaceutical Industry topics, issues, challenges and way forward w.r.t. Pharmaceutical E-governance systems, processes with keen objective to provide learning and practical opportunity to Pharmaceutical Professionals.

This workshop focus with detailing practical Hands on, Case Studies and Personal attention.


15th May, 2020

Organized by:-

Workshop Trainers

Industry & Regulatory Expert

Industry Regulatory Expert

Speaker 1

Dr. Sarika Pardhe

CEO & Principal Regulatory Consultant, AblyReg Advisory, Mumbai, India.

Regulatory Expert from FDA

Speaker 2

Mr. Omprakash Sadhwani

Ex. Joint Commissioner Food and Drug Administration Maharashtra.

Regulatory Expert

Speaker 2

Mrs. Punam Gupta

Director- Quality Services and Training Pvt. Ltd.  &  General Sec- Rab Di Mehar

Regulatory Expert

Speaker 2

Mrs. Mamta Sharma

Regulatory Expert

Workshop Schedule

Here is our Workshop Schedule

Opening Session

Welcome & Introduction of Workshop Trainers

Session-1 (Dr. Sarika Pardhe)

-Master the Art of Regulatory Professionals – Role, Responsibilities & Skills

- Surface Disinfectant Regulatory Requirements-An Overview

Session- 2 (Mr. Omprakash Sadhwani)

-New Drugs and Clinical Trial- Mystery Un-Corded. (45 min)With special focus on BA-BE Studies in Pharmaceutical Industry.

Special Insights on: (30 min)

- Effectiveness of State Govt. through E- Governance with respect to Regulatory Affairs.

Session – 3 (Mrs. Mamta Sharma)

-Indian Regulatory Landscape & Scenario - Current Changes In Drugs, Cosmetics & Medical Devices.

- Be Smart- How to Manage Product-Life Cycle in Electronic Way?

- Sugam Portal Benefits & Way forward.

Session – 4 (Mrs. Punam Gupta)

An Effective Ways for FSSAI Submissions and Neutraceutical Procedure

Closing Session

Thanks Note

Media Partners

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