Surviving an FDA Good Laboratory Practices (GLP) Inspection – Critical Tips For Compliance0 Available
This 90-minute course will provide you with the tools to understand proper conduct of GLP studies, safeguard against inspection deficiencies, and satisfy regulatory agencies that your efforts are compliant.
The Global Development Plan (GDP): Your Roadmap To Drug/Device Development
This webinar will look at the different components of a development plan and review the information needed to capture the essence of your project. Additionally, this course will enable you to have an appreciation and understanding of the processes and the various facets associated with planning for successful drug development.
The New Medical Device Single Audit Program (MDSAP) for Manufacturers – Analyzing Rewards and Challenges0 Available
In the highly regulated medical device world, standards and regulations are continuously evolving to ensure that the highest levels of quality and safety are achieved. To that end, international regulators have long recognized the value of developing a standardized, global approach to auditing and monitoring medical device manufacturing, and for the last five years, the International Medical Device Regulators Forum (IMDRF) has spearheaded an effort to create such a framework.
The Power of Influencing – Achieving Patient-focused Outcomes to Guarantee Success0 Available
Join us for this 60-minute webinar with engaging speaker Jill Donahue, HBa, MAdEd, author of the award-winning mobile program EngageRx: The 3 Keys to Patient-focused Growth. Jill is passionate about helping lift pharma; helping us learn how to become trusted, valued partners to healthcare professionals.