Is your OSD containment strategy fit for purpose?
Assess risks. Identify the right containment solution.
Effective containment goes beyond equipment selection. It requires an understanding of manufacturing risks, compliance expectations and the measures needed to demonstrate effective containment.
Join Particle Measuring Systems and ACG for a technical webinar exploring the role of environmental monitoring and containment solutions in high-potency pharmaceutical manufacturing. Learn about key considerations for assessing containment performance, demonstrating compliance and identifying suitable equipment solutions for your manufacturing needs.
Key Learning Objectives:
- Understand environmental monitoring requirements for high-potency products in isolator environments.
- Explore how monitoring helps demonstrate containment and identify potential leakage.
- Understand key compliance considerations, including EU GMP Annex 1 and ISO 14644-1.
- Explore containment solutions and key considerations for selecting suitable equipment for pharmaceutical manufacturing.
Who should attend this webinar:
- Pharmaceutical manufacturing and production
- Engineering and equipment selection
- Quality assurance and regulatory compliance
- Environmental monitoring and contamination control
- EHS and facility operations
Speakers
Mark Hallworth
Global Pharma and Sr. GMP Advisor, Life Sciences Division
Mark Hallworth is a globally recognized authority in pharmaceutical contamination control, specializing in the design, validation, and implementation of GMP-compliant environmental monitoring systems. With decades of experience, he has led more than 200 projects across cleanroom facilities, focusing on regulatory compliance, data integrity, and system performance. Mark has contributed to the development of particle counters for hazardous environments and 21 CFR Part 11ācompliant software for batch release and test management. He has authored over 100 technical papers and contributed to leading industry publications and reference books. Mark frequently presents at international forums, including the Parenteral Drug Association (PDA) and ISPE, where he teaches best practices in cleanroom monitoring and GMP compliance. Additionally, Mark served on the ISO 14644-21 technical committee and received the IEST James Mildon Award for advancing knowledge in contamination control. His work continues to shape standards and practices across the global pharmaceutical and biotechnology industries.
Dhiraj Sonavane
Product Manager Process Equipment, ACG Engineering
