PDA India Chapter Annual Meeting – Maintaining Quality & Compliance in Pharmaceutical Drug Manufacturing and Regulatory Expectations – Being Held March 11-15, in Hyderabad, India




PDA India Chapter Annual Meeting – Maintaining Quality & Compliance in Pharmaceutical Drug Manufacturing and Regulatory Expectations – Being Held March 11-15, in Hyderabad, India

PQE Group to Sponsor, Present Technical Content Exhibit, and Attend Conference

HYDERABAD, India–(BUSINESS WIRE)–PQE Group is excited to join the 2024 PDA India Chapter Annual Meeting in Hyderabad from March 11-15, focusing on key issues in the pharmaceutical and medical device industries.

The conference will cover environmental monitoring, aseptic processing, cleaning validation, cross-contamination, and compliance strategies in the pharma and medical device industries, with insights from regulators and experts on technologies, data integrity, and quality enhancement.

On the first day of the conference, the opening plenary sessions will feature opening remarks from Dr. Sarah McMullen, Country Director, US FDA India Office, Alonza Cruse, Director, Office of Pharmaceutical Quality Operations, ORA/FDA, Dr. Anil Sawant, Senior Vice President, Global Quality Compliance, Merck Sharpe & Dohme, USA and Chair, Board of Directors, PDA Inc, a Regulatory Update will be provided by Dr. Carmelo Rosa, Director Division of Drug Quality I, CDER/OMQ/US FDA and Co-Chair, PDA India Chapter and many other exciting regulatory presenters. Annual Meeting Day One will also focus on Quality Culture, with sessions including topics regarding several aspects of the importance of Quality Culture, Quality Sustainability, and Quality Maturity, which will be led by presenters including Dr. Rosa, Dr. G.K. Raju, Chairman and CEO, Light Pharma Inc., Stephen Tyrpak, Vice President Operations, PQE US Inc, and Dr. Deva Puranam, Head – Global Quality Investigations, Surveillance & Regulatory Communications, Viatris.

The “Back to Basics” workshop on March 14-15, hosted by US FDA and industry experts, will discuss key regulations and guidelines to help participants understand regulatory expectations for sustainable operations. In addition, Stephen Tyrpak will lead sessions on Quality Culture, risk management, and visual inspections with case studies and demos. FDA and EDQM regulators, along with other experts, will conduct various sessions throughout the conference.

“We’re thrilled to take part, present, and support this significant event, which has become increasingly valuable for the pharmaceutical and medical device industries in India. Since PQE Group’s launch in India in 2019, we’ve grown to over 110 professionals dedicated to compliance across the region. We eagerly anticipate a productive and educational week in Hyderabad, looking forward to reconnecting with peers and forging new partnerships at booth #7.” said Mahesh Jagtap, PQE India local partner.

Contacts

Media Contact:

Debra Kaufmann – d.kaufmann@pqegroup.com; +1.240.704.0550