Friday, November 7th, 2025 @ 3 PM IST

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Top Reasons to Attend this webinar

Understand the New Compliance Landscape

Schedule M—now aligned with WHO, USFDA, EU-GMP, and PIC/S standards—and what it means for your facility.

Master Risk-Based GMP Principles

Learn how to implement core elements like Pharmaceutical Quality Systems (PQS), Quality Risk Management (QRM), and Product Quality Reviews (PQR).

Get Clarity on Timelines & Implementation

Know exactly what’s required and by when—especially for small and large manufacturers facing the December 2025 deadline.

Prepare for Modern Manufacturing Demands

Understand new requirements for computerized systems, contract manufacturing, and niche products like biologics and radiopharmaceuticals.

Interactive Q&A Session with Dr. Ashwini and Subject Experts

Understanding the New Schedule M Guidelines

We are regulatory solutions provider catering to a vast array of services and products to simplify, familiarize and support our clients through every step of the Regulatory process.

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Join us in this webinar to understand the revised Schedule M and elevate your GMP compliance to global standards.

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Featured Speakers

In this Upcoming webinar, meet our experts to Understand it and Implement it.

Dr. Ashwini Kumar

Founder & CEO

Nidhi Dixit

Senior Executive- Regulatory affairs

Vijay Maurya

Sr. Manager - Regulatory Affairs

Frequently Asked Questions

Who is this webinar for?

This session is ideal for professionals in pharmaceutical manufacturing—including QA/QC personnel, Regulatory Affairs specialists, Plant Heads, Compliance teams, Validation experts, and pharma entrepreneurs—who need to align with the latest GMP standards under the revised Schedule M.

What will I learn from this webinar?

You’ll gain a clear understanding of the major changes in Schedule M (2023), including Quality Risk Management (QRM), Pharmaceutical Quality Systems (PQS), Product Quality Review (PQR), and new requirements around contract manufacturing, computerized systems, and more.

Is the revised Schedule M applicable to my company?

Yes, if you are licensed to manufacture drugs in India, the revised Schedule M applies—especially if your operations involve sterile injectables, oral solids, biologicals, or other regulated product categories. Timelines vary based on company turnover and product type.

Will I receive a certificate of attendance?

Yes, all registered participants who attend the webinar will receive an official Certificate of Participation.

How do I register and is there a fee?

Registration is simple—just click the registration link on this page and fill out your details. The webinar is completely free to attend.

Who all should attend this webinar?

Pharma Entrepreneurs, SMEs & Exporters
Manufacturing Heads & Plant Managers
Quality Assurance (QA) & Quality Control (QC) Professionals
Validation, Engineering & Compliance Teams
Regulatory Affairs Specialists

Aligning with Global Standards: Understanding the New Schedule M Guidelines