It was observed that there are misunderstanding between design intent HVAC designer and User (who is working on the field) where each party is focusing on his area! HVAC designer focus on the Engineering design aspects and User (on the other side) focus on cGMP aspect!!, in this course we will discuss the cGMP HVAC design criteria that could be create a base and common understanding between two parties and finally achieve ideal common understanding.
This course will address that Implementing ideal cGMP criteria when designing HVAC in conjunction with GEP requirement is essential so that the facility will achieve better compliance and in the same time will avoid mistakes that could be raised during lifecycle of the systems.
Areas Covered in the Session:
Who Will Benefit:
Majdi is dedicated and results-driven Q&V expert with a highly successful background with Pharmaceutical companies in both project and operation fields to achieve the best possible performance through the creation and execution of successful and creative Q&V strategies.
He worked with different departments within Pharmaceutical Engineering Fields, During his experience for the last 16 years, he had implemented different GxP concepts including: Engineering Designs; Setup Project Policy & Engineering Quality systems; Implementation of Equipment Qualification and Calibration for: Production Systems, Facilities Management and Infrastructures ,utilities for both sterile/ non-sterile facilities as well as API’s facilities ; along with his experience for preparation and attendance different inspections by local/international authorities (FDA,EU and Local …..And others.)
NetZealous - Compliance4All,
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539, USA.
Event Link : http://bit.ly/1Fenw4m