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    The Best Way to Develop or Improve a Master Validation Plan

    View: 140

    Website https://www.onlinecompliancepanel.com/webinar/DEVELOP-IMPROVE-MASTER-VALIDATION-PLAN-507598/AUGUST-2 | Want to Edit it Edit Freely

    Category Master Validation Plan, Medical device validation, validation master plan, validation master plan for pharmaceutical industry, master validation plan, pharmaceutical process validation, equipment validation process, process validation guidance, medical device design validation protocol, medical device manufacturing process validation, equipment validation procedure, master validation plan for pharmaceutical, process validation sampling and testing plan, validation of manufacturing process in pharmaceuticals.

    Deadline: August 30, 2017 | Date: August 31, 2017

    Venue/Country: California, U.S.A

    Updated: 2017-08-16 18:46:21 (GMT+9)

    Call For Papers - CFP

    This webinar provides the creation, implementation, and maintenance of Validation Master Plans. Join for the webinar by the expert speaker Kevin Posey.

    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.