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    "CAPA Training and Causes of Warning Letters due to Lack of Comprehension"

    View: 11

    Website https://compliance2go.com/product/?pid=CP2014-340 | Want to Edit it Edit Freely

    Category online

    Deadline: July 23, 2014 | Date: July 23, 2014-August 01, 2014

    Venue/Country: Houston, U.S.A

    Updated: 2014-06-17 15:03:00 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    CAPA (Corrective and Preventative Actions) did not originate in the Pharmaceutical and Medical Device industry or the Automobile Industry as most folks post on the Internet. The program to make effective corrections and ensure that preventative applications were incorporated was in use way back in the 60s by NASA and the FAA to enhance safety but was not labeled CAPA even though the intent was the same.

    Why should you attend?

    A vast majority of the current industry deficiencies which have led to isolated 483s, Warning Letters and Consent Decrees are the result of deficient technical documentation and effective means of assessing various elements of CAPA expectations for products produced and distributed under the FDA regulations.

    For any assistance contact us at supportatcompliance2go.com or call us at 877.782.4696 Or Visit us:-https://compliance2go.com/product/?pid=CP2014-340


    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.