With tightening regulatory expectations for sterile product quality and safety based on patient risk, the 2018 PDA Sterile Medicinal Products Manufacturing Conference, May 14-15, is a “must-attend” for anyone involved in sterile manufacturing.

Don’t miss out – early registration savings end soon!  

Register by Mar. 5 to save on this exciting Conference exploring on a wide variety of topics related to sterile manufacturing. Take advantage of case studies and personal experiences from industry and regulatory experts, with special reference to the recently released draft revision of the EU GMP Annex 1, to stay up to date with important advances in the field.

• Risk- and science-based assessment and approaches in sterile product facility design and manufacturing processes
• Modern methods for cleanroom qualification, environmental monitoring, and contamination control
• How to better use existing sterile product technologies
• PDA and industry responses to the proposed revision to Annex 1 and other regulatory trends and expectations
• New thinking on sterile product manufacturing validation and aseptic process simulation

Be part of the important dialogue between manufacturers, suppliers, and regulators working together to solve issues and improve sterile manufacturing processes for the future!

Parenteral Drug Association (PDA)
4350 East West Highway, Suite 600
Bethesda, MD 20814 USA
Tel: +1 (301) 656-5900
Fax: +1 (301) 986-1093
www.pda.org

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