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GMP Fundamentals of Pharmaceutical HVAC :System This part will discuss the benefits of HVAC system in pharmaceutical industries as well as discussing the contamination sources that must be prevented where this section will give information about how bad HVAC can be risky on both process or humane comfort as well
Introduction about the cGMP Design Concept for HVAC system: This part will give introduction about the Impact assessment on HVAC system, and will also discuss the main User requirement specifications (URS) and design criteria needed to be considered when designing new cGMP HVAC system that in turn will meet with intended purposes that are relevant to pharmaceutical process.
This section will also address some HVAC layouts example detailing configuration for design of different pharmaceutical dosage forms within pharmaceutical plants.
Why should you Attend: 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: