Quality testing of Medical Devices ranges from syringe actuation (break loose and glide), needle sharpness and adhesion strength to Child Resistant Closure (CRC) torque. Even though there are different approaches to these test applications, one thing remains true – the need for compliance to 21 CFR Part 11.
21 CFR Part 11 governs the access to, creation, modification and deletion of data to ensure data integrity.
This webinar with will focus on the importance of Medical Device testing - methods and applications, while showing you how to achieve compliance to 21 CFR Part 11.
What You’ll Learn:
Who Should Attend:
Manufacturing, production and quality workers and engineers involved in Medical Device testing, with a particular emphasis on 21 CFR Part 11 compliance.