Visit with Lachman Consultants at Booth #314 during the event.
We hope you’ll be joining us at the annual PAD/FDA Joint Regulatory Conference on September 9th-11th at The Westin Washington, DC Downtown. This years can not miss event is entitled Current Good Manufacturing Practice (CGMP): Leading with Quality and Integrity,” and will provide in-depth knowledge and practical understanding through focused sessions, interactive discussions, regulatory updates, and case studies regarding the CGMP requirements of the FDA.
The PDA/FDA Joint Regulatory Conference 2024 is celebrating its 33rd year of informing, educating, and guiding industry professionals and organizations. This CGMP conference emphasizes the role of effective quality systems in ensuring an ongoing state of control throughout the product lifecycle by diligently managing risks to manufacturing and quality.
The vital role of robust quality systems, facilities, processes, raw material quality, supplier relationships, industrial modernization, and quality risk management, is emphasized as fundamental to assuring Current Good Manufacturing Practice (CGMP) compliance. Case studies presented throughout the conference will provide practical insights and illustrate how sustainable compliance establishes the foundation for quality and supply consistency.
Scheduled to attend from Lachman Consultants are Frances Zipp, President & CEO; Linda Evans O’Connor, Vice President; and Matt Taylor, Director, Marketing & Client Engagement.
To schedule a meeting with Lachman Consultants at the conference, click here
Registration for the 33rd Annual PDA/FDA Joint Regulatory Conference is currently open.
For more information and to register, visit: https://www.pda.org/global-event-calendar/conferences/pda-fda-joint-regulatory-conference-2024
