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

    View: 48

    Website https://www.complianceonline.com/equipment-qualification-dq-iq-oq-pq-process-validation-vmp-seminar- | Edit Freely

    Category

    Deadline: August 08, 2020 | Date: August 18, 2020-August 19, 2020

    Venue/Country: U.S.A

    Updated: 2020-07-03 03:37:52 (GMT+9)

    Call For Papers - CFP

    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?


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.