GlobalCompliancePanel

A RAPS pre-approved webinar on the topic, “Project Management for Computer Systems Validation” is being organized by GlobalCompliancePanel, a leading provider of regulatory and compliance continuing education training, on March 14.

Validation is not where atest method or manufacturing process ends. After this has been done, there is a need to continuously demonstrate that the procedure will operate consistently and reproducibly in a manner that meets the validation requirements

Cleanroom cleaning is a vital aspect of a medical product. Since it is in cleanrooms that medical products are made; cleanroom cleaning is very important to ensure product approval.

“Medical Device Adverse Event Reporting Systems in EU, Canada and US” is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 6.

GlobalCompliancePanel,a leading regulatory and compliance training gateway,will host a two-day, in-person seminar on the topic, “Good Laboratory Practice Regulations” on March 21 and 22 at Mumbai, India.

This webinar is a learning session on how to implement steps with which to ensure that controls are put in place. All these were quite loosely put in place; from now on, there is strict requirement on minute aspects, too.

A 510 (K) premarket notification is the most common route to the market for a medical device, including in-vitro diagnostics (IVD’s).

An unfortunate, yet undeniable fact of water systems is that many of them are designed keeping obsolete concepts in mind. The result of an organization’s reluctance to update its water systems is that the systems are built on a shaky foundation.

Adaptive clinical trials, owing to their flexibility, help bring in the latest technological findings midway through into a clinical trial. This helps improve the end result quite dramatically.

This webinar will help participants explore the design considerations for cleanrooms. It will also offer insights on certification and validation strategies based upon tried,tested and validated industry practices, guidelines, and standards.