Version 2.0
Last update on 30/07/2024
Master Device Qualification in pharma and medical industries. Learn to ensure device integrity and compliance with essential FDA and EMA regulatory standards.
Version 2.0
Last update on 30/07/2024
Last update on 30/07/2024
Explore the critical world of Device Qualification in the pharmaceutical and medical device industries with our comprehensive course. This educational journey delves into the essentials of device qualification, ensuring that professionals grasp the importance of verifying and validating equipment used in production. Understand the regulatory standards, including FDA and EMA guidelines, and master the process of ensuring devices meet these stringent criteria. Our course is ideal for those in quality assurance, engineering, and manufacturing roles, providing the knowledge needed to ensure device integrity, safety, and compliance. Equip yourself with practical skills and in-depth understanding, crucial for maintaining the highest quality standards in healthcare product manufacturing.
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This course has been desgined with learning objectives at the heart of it, so you can be assured to walk away with a valuable new knowledge set. After completing this course, you will be able to:
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