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Wuhan, China
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Shenzhen, China

Mar
24

Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing

 
 Seminar/trade show (noCPF)

When:

  24 Mar 2021 through 25 Mar 2021

Where:

  Online Event | United States

Website URL:

  https://www.complianceonline.com/equipment-qualification-dq-iq-oq-pq-process-validation-vmp-seminar-training-80295SEM-prdsm?channel=Brownwalker

Sponsoring organization:

  Compliance Online

Categories:

  Engineering & Technology - Mechanical/Industrial

Keywords:


Event description:

The various regulatory agencies have expectations that pharmaceutical manufacturers will demonstrate control over their manufacturing equipment. The FDA's findings of deficiencies concerning equipment validation indicate the agencies expect definitive evidence that the equipment qualification and validation schedules of a facility will satisfactorily control their manufacturing processes. Examples of FDA form 483 findings for equipment qualification and validation indicate deficiencies in many of these studies. The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for equipment qualification and validation in your manufacturing facility? In this two day workshop conference you will learn the different global agencies expectations of equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and effici... Read more

Posting date:

17 February 2021  |  217 views

Placement:

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