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    Are you aware FDA’s New Import Program : Be Prepared and Be Compliant

    View: 86

    Website https://worldcomplianceseminars.com/upcoming_webinar | Edit Freely

    Category Legal Counsel, Regulatory Management/ SME/Affairs/RA Specialists, Purchasing, Quality, Auditors, Compliance, Technical Services/Operations, Project Management, Business Planning Executives

    Deadline: January 29, 2020 | Date: January 29, 2020

    Venue/Country: Online Webinar, U.S.A

    Updated: 2020-01-04 17:21:02 (GMT+9)

    Call For Papers - CFP

    The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole process easier. The FDA and U.S. Customs and Border Protection (CBP) are relying more and more on computer programs to expedite the import process. The new import entry filing requirements became effective in 2016 and is posing problems for the user. Failure to provide the correct information creates costly delays.

    Learning Objective:

    The webinar focuses on FDA's software screening program, PREDICT, and U.S. Custom's ACE program that require careful attention for being prepared and compliant.

    Speaker Profile:

    David R. Dills, is currently the Director of Regulatory Services at CROMSOURCE, an international contract research organization (CRO to the pharmaceutical, biotechnology, and medical device industries


    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.