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    ONLINE WEBINAR 2016 - Trial Master File (TMF): FDA Expectations from Sponsors and Sites

    View: 127

    Website http://onlinecompliancepanel.com/webinar/TRIAL-MASTER-FILE-FDA-EXPECTATIONS-SPONSORS-SITES-501613/AU | Want to Edit it Edit Freely

    Category TMF, Trial Master File, Trial Master File for a clinical trial, TMF for a clinical trial, FDA audit, creating TMF, Maintaining TMF, errors in TMFs, TMF errors, ICH E6 Good Clinical Practices, ICH guidelines, Good Clinical Practice, ICH E6 Good Clinical Practices, Food and Drug Administration, ICH Guidelines, trial documentation, electronic trial master files

    Deadline: August 23, 2016 | Date: August 24, 2016

    Venue/Country: CA, U.S.A

    Updated: 2016-07-22 17:56:45 (GMT+9)

    Call For Papers - CFP

    How to create and maintain a Trial Master File for your site or clinical trial ad what are the critical components of a TMF? Attend this webinar to understand TMF better.

    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.