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.  


Click Here to Register