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Join PDA for one or more of our fall events. As a leading provider of education and technical resources to the bio/pharmaceutical manufacturing industry, PDA offers the very latest on the hottest topics in the industry.
Choose from an exciting lineup of Conferences and Workshops:
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2017 Annex 1 Workshop | Oct. 2-3, Washington, DC
Attend this Workshop to gain an in-depth understanding of the revision to EU GMP Annex 1: Manufacture of Sterile Medicinal Products from the experts who authored it. Learn how this new guidance will impact sterile manufacturing processes globally. Attendee feedback on Annex 1 revision will be shared with regulatory authorities. Register now! |
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2017 PDA Container Closure, Devices, and Delivery Systems: Compatibility and Material Safety Workshop | Oct. 2-3, Washington, DC
Join industry and regulatory experts as they examine the challenges associated with novel combination products and brainstorm practical solutions to address them. Select topics to be covered include the future of drug delivery, strategies for safety evaluations, and compatibility of delivery systems with biologics. Register now! |
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12th Annual PDA Global Conference on Pharmaceutical Microbiology | Oct. 16-18, Bethesda, MD
This "best-in-class" conference features an exciting agenda encompassing a wide range of issues that pharmaceutical microbiologists face daily and work in partnership to solve. Hear the latest on quality management for the microbiology lab, updates from USP, innovations in pharmaceutical microbiology, U.S. FDA update on Human Drug Compounding, and how the future of biotech will create new manufacturing challenges. The interactive "Ask the Experts" session is back by popular demand! Register now! |
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2017 PDA Endotoxins Workshop | Oct. 18-19, Bethesda, MD
Discover the latest advances in endotoxin control and learn testing methods to manage possible endotoxin contamination. Expert presenters will tackle such topics as data integrity, practical issues with endotoxin testing, determining endotoxin limits for raw materials, and the regulatory perspective regarding the Monocyte Activation Text. Case studies will illustrate best practices for setting endotoxin specifications, with opportunity for discussion of problems and potential solutions. Register now! |
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2017 Visual Inspection Forum | Oct. 23-24, Bethesda, MD
Share new developments and trends in the visual inspection process with experts and other professionals in the field. Gain practical tools from case studies and explore new USP chapters <790> and <1790>. Discuss the latest in sampling and inspections processes, practical aspects of manual and automated methods, and the regulatory and compendial requirements that govern them. Register now! |
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2017 PDA Cell and Gene Therapy Conference | Dec. 5-6, San Diego, CA
Don't miss this seminal Conference on one of the most exciting and rapidly evolving facets of the pharmaceutical field. The development and commercialization of these new products requires new approaches to manufacturing. Experienced industry and regulatory experts will share with you the science and technology necessary to bring your cell and gene therapy products to market and, ultimately, to the patient. Explore next-generation processes and facilities and the application of big data to process design and optimization, and the acceleration of the industry response to healthcare needs. Learn how to maximize your company's potential opportunities in this emerging field. Register now! |
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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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