planurevents

...Therefore, Design Controls are considered a critical process by the FDA. Yet, Design Controls are still one of the most frequent areas for 483 and Warning Letter observations... Learn about: Medical Science, Medical training...

...guidance documents for early stage manufacturing and GMPs in detail. Regulatory strategies and logistical considerations for early development stage product... Learn about: Best Practice...

...Managers who want to broaden their perspective, improve flexibility without compromising quality and increase their department’s value to the organization... Learn about: Quality Training, Best Practice...

...documents can further concurrent development and/or updates to both. Why you should attend This webinar will examine the existing and proposed requiements for the... Learn about: Best Practice...

...An overview of a comparative analysis will be presented comparing SAMHSA to the HIPAA laws relating to protected health information in general. This 6-hour... Learn about: Best Practice...

...in a development process, Design Control begins will be answered. The differences between pre release and post release change control will be explained... Learn about: Best Practice, IT risk...