This PDA/FDA co-sponsored workshop will explore how various sectors of the regulated industry have adapted to the emerging global culture and address the benefits of modernization and innovation as well as the ongoing challenges of supplier (CMOs, ingredients) management. Register Today!
We will bring together industry professionals and regulators to explore new and improved strategies for sterile product manufacturing technologies. It will provide participants with a comprehensive review of contemporary practices for the conduct of terminal sterilization and aseptic processing with emphasis on process simulation, risk assessment/mitigation, and parametric release. Register Today!
The Global Pharma Manufacturing summit is one of North America’s leading annual events, attracting over 200 senior manufacturing professionals to discuss the current challenges, develop improved manufacturing strategies and analyze the latest case studies. Learn more at www.gpmsummit.com or call (416) 214-1144.
This conference offers the unique opportunity for you to join FDA representatives and industry experts in face-to-face dialogues. FDA speakers will provide updates on the current state of efforts impacting the development of global regulatory strategies, while industry professionals will present case studies on how to employ global strategies. Register Today!
BioBasics is a two-day course for the non-scientist which highlights science and technology concepts that are the basis of the biotechnology industry. The course is for participants that require a working knowledge of fundamental terms and applications. Register today.
This post-conference workshop to PDA's Joint Regulatory Conference is designed to deliver practical solutions to improve quality investigations. Hear FDA specialists and industry experts speak about the root causes of poor investigations and share their insights on how to lead to improvement to quality and compliance. Register Today!
This workshop will bring together industry professionals to benefit from updates on recent regulatory guidance's regarding developing and validating analytical methods. We will provide a comprehensive review of laboratory and documentation standards. All paid attendees will receive a free e-copy of PDA Technical Report No. 57, Analytical Method Validation and Transfer for Biotechnology Products. Register Today!
This conference will provide interactive case studies, explore USP <790>, and discuss new developments in the field of visual inspection, including a basic understanding of the sampling and inspection process, practical aspects of manual and automated methods, and the regulatory and compendial requirements. Register Today!
This conference will reveal the essential science of microbiology and seeks to solve the problems that our industry faces on a daily basis. The comprehensive program agenda will include presentations from regulatory and industry representatives from around the world who will share recent case studies, and current and future trends in the field of pharmaceutical microbiology. Register Today!
A one-day class delivering an overview of the discovery, development, and regulatory processes for bringing a new drug to market. Participants will learn about the business and scientific decisions involved in moving a product forward from basic research into preclinical and clinical trials. Learn More.
This conference will include presentations and panel discussions from regulatory and industry representatives who will share recent case studies, emerging trends, and hot topics in the industry. It will provide an engaging forum for regulatory, industry and academic colleagues to discuss and integrate current and emerging strategies for controlling viral contamination. Register Today!