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Promotional banner for Pharmig India 2025 showing event dates in Ahmedabad on 2 December 2025 and Hyderabad on 4 December 2025, with background images of the Statue of Unity and Charminar.

What to Expect at Pharmig India 2025

Pharmig India 2025, taking place this December in Ahmedabad (December 2nd) and Hyderabad (December 4th), promises to be India’s premier summit for contamination control in the pharmaceutical and biopharmaceutical sector.

In partnership with PharmaNow, a leading media and events platform, the conference brings together industry experts and regulators for two days of insight and professional collaboration. Here’s what you can expect…

Pharmig India: A Hub for Industry Knowledge

Attendees can expect a carefully curated programme that goes beyond traditional presentations. Leading local and international experts will tackle pressing topics in pharmaceutical microbiology, including environmental monitoring, contamination control strategies, and data integrity.

Through a combination of presentations, case studies, fireside chats, and interactive workshops, delegates will gain practical guidance they can implement directly in their facilities.

Key sessions include:

  • Fine-tuning your Environmental Monitoring programme – Dr Tim Sandle from Pharmig provides insights on optimising EM practices.
  • Contamination Control Strategy (CCS) – Patrick Nieuwenhuizen from PharmaLex highlights how CCS can improve both sterile and non-sterile operations.
  • Data integrity in practice – David Keen of Ecolab leads a fireside discussion on maintaining compliance and trust in the era of stricter regulations.
  • Air visualisation workshops and group exercises – Practical sessions led by Manish Bhatkar from Red Lotus allow attendees to see contamination control concepts in action.
  • How does air visualisation fit into your overall microbial control (workshop) – Manish Bhatkar, Red Lotus
  • Group exercises – practical exercises on pharmaceutical microbiology

Why India is Critical to Pharmaceutical Microbiology

India plays a critical role in global healthcare, supplying over 60% of the world’s vaccines and  hosting the largest number of US FDA-approved plants outside the US.

With the implementation of EU GMP Annex 1, regulatory expectations have risen sharply, placing microbiology and contamination control at the centre of compliance.

For QA, QC, and regulatory professionals, keeping pace with these standards has never been more crucial.

Networking and Live Demonstrations at Pharmig India

Pharmig India 2025 is about the latest best practices and learning. However, we also believe that industry connections and networking are at the heart of the event.

The event is invite-only and curated to ensure high-value interactions. Delegates will meet a focused audience of over 300 senior professionals, including QA and QC heads, microbiology managers, and regulatory affairs leaders.

Live demonstrations and interactive sessions provide a rare chance to engage directly with industry veterans and regulators, gaining insights into real-world applications of contamination control strategies.

Final Thoughts

By the end of the summit, participants will leave with actionable guidance on designing and implementing contamination control strategies, best practices for environmental monitoring, root-cause analysis skills, and an understanding of emerging trends shaping pharmaceutical microbiology.

More than that, attendees will return to their workplaces better equipped to ensure compliance and drive innovation in their organisations. And, of course, some positive memories!

Learn more about Pharmig India 2025 here.

Or for more information, visit PharmaNow’s Pharmig India 2025 page.