Complying to ever evolving global requirements of emerging markets and meeting regulatory expectations of a well evolved landscape is vital to maintain the safety & efficacy of the new & existing drugs, and accuracy of product information. Eminence Business Media acknowledges this need and after conducting several successful conferences, liked, and appreciated by the pharma fraternity, we are coming up with the inaugural program Pharma Regulatory Conclave 2023 in Hilton, Goa.
PHARMA REGULATORY CONCLAVE 2023
HILTON, NORTH GOA
Virtual : 30th June, 2023
In-Person : 5th - 6th July, 2023
This program will be a reference guide for identifying the challenges and underlying opportunities in the regulatory framework, for overall growth in aspects of essential documentation, preparing the dossier efficiently and filing the global application, followed by unparalleled business & research opportunities, networking platforms, and access to new trends in the Indian pharma world.
At this forum, top issues highlighted by the regulators will be addressed by the pharma experts & key people from regulatory bodies, as they share their insights, experiences and use case studies on updated regulations & policies, maintaining data in the information system, ensuring compliance with regulations, and evaluating applicable laws to determine impact on company activities.
This is your best opportunity to arrive and meet the biggest array of members from the regulatory and related departments. Network with your industry peers, discuss the new trends, strategies, and solutions, and meet the apt partners to take home the most relevant learning to help you grow and meet your company goals. Let's connect and together build the Pharma Regulatory Conclave 2023.
WHY ATTEND?
1. Take advantage of the dedicated day 0 webinar a week prior to the in-person event, with extensive opportunities to clarify your doubts.
2. Discuss your queries during dedicated Q&A sessions and reap the benefit from the extended 6-month support for continuous learning.
3. Solve live case studies & deliberate on the shortcomings and practical solutions.
4. Network with the industry leaders to understand what they do differently to be successful.
WHO SHOULD ATTEND?
MD, Directors, CXO’s, President, Sr. VP’s, VP’s, GM’s, Heads, Leads, Managers and professionals from:
1. Regulatory Affairs
2. Regulatory Operations
3. Research & Development
4. Manufacturing & Supply Chain
5. Quality Teams
6. Academia
7. Everyone who needs to comply with regulatory guidelines, managing database, product information and filing dossier.
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