Location: Philadelphia, PA
STERIS Life Sciences is proud to be part of the Process Validation Summit in Philadelphia, PA. During this extensive two-day seminar industry leaders will help explain FDA requirements for process validation to help ensure FDA compliance. A variety of topics will be covered including a presentation from our own Technical Services Manager, Elizabeth Rivera.
Stage 1: Process Understanding, Define Process Control and Success for Continuous Improvement
Friday, May 18 at 8:30AM by Elizabeth Rivera
Description: Covering different GMP requirements regarding ‘stage 1’ process validation, this presentation will also detail and explain the changes of recently effective process validation EMA guideline on process validation.