The Pharma Industry Is Evolving—So Should Your Knowledge
Establishing and maintaining an appropriately skilled workforce for the future is one of the biggest difficulties facing international pharmaceutical corporations today. The workforce composition and skills requirements are also changing due to technological innovations in drug manufacturing, such as automation and multifunctional manufacturing sites. These new opportunities and challenges make keeping your knowledge up to date more crucial than ever.
Continuous professional development can assist you in supporting your company in producing effective medicines under the strictest manufacturing standards and providing quality, lifesaving drugs worldwide. The importance of continuing education is further intensified by the demand to get products to market faster while still maintaining best practices and meeting regulatory requirements.
ISPE is committed to the advancement of the educational and technical efficiency of our Members and the pharma industry through forums for the exchange of ideas and practical experience. ISPE’s training courses are a core resource for industry professional as we leverage subject matter experts and top leaders in the pharmaceutical industry to bring their knowledge and experience to the coursework, presenting exercises that use current problems and situations common to the pharmaceutical industry.
ISPE’s upcoming 2019 Cambridge In-depth Pharma Training Series will take a deep into four critical areas of pharma manufacturing, offering unparalleled professional development through lectures, case studies, complimentary guidance documents, and group exercises.
Register today to secure your seat for one of these topic-focused courses near one of the top pharma hubs in the US.
GAMP® 5, Annex 11/Part 11 Basic Principles
24-26 Jun 2019
This two-day or three-day fundamental course introduces attendees to agency regulation requirements for complex computerized systems in the pharmaceutical industry and explores tested and internationally recognized methods of meeting new requirements. GAMP® guidance provides an effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements.
Overview Biotechnology Manufacturing Processes
24-25 Jun 2019
This course provides a comprehensive understanding of biotech manufacturing processes - what makes biopharmaceutical processes different from small molecules. Course content explores the underlying principles of proteins and cells to provide the foundation for how and why processes manufacture therapeutic proteins.
GAMP® 5 GxP Process Control
24-25 Jun 2019
This highly interactive classroom course describes how the GAMP® Good Practice Guide: A Risk Based Approach to GxP Process Control Systems, may be applied to achieve process control systems that are fit for intended use and meet current regulatory requirements. The course covers recommended good practice based on a lifecycle approach for the development and management of process control systems and shows how the principles and concepts of GAMP® 5 may be practically applied to process control systems.
Process Validation
24-26 Jun 2019
This classroom course is relevant to individuals working throughout the pharmaceutical product lifecycle in development, manufacturing, quality, and many other roles involved in validation of products and processes. It will help you integrate the science and risk-based lifecycle approach for Process Validation to your overall Pharmaceutical Quality System. The course will provide a practical application of quality risk management tools in preparation and planning for validation of your manufacturing control strategy.
