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    Blue Print for Implementing Pharmaceutical and Medical Device Quality Management System under one Umbrella

    View: 110

    Website http://onlinecompliancepanel.com/webinar/DEVICE-QUALITY-MGMT-SYSTEM-501262/FEB-2016-ES-OURGLOCAL | Want to Edit it Edit Freely

    Category FDA Regulated industry quality requirements, Pharmaceutical quality management system requirements, Medical Device quality management system requirements, Quality and Regulatory Requirements Combination devices, Amalgamated Quality management system for ISO 13485 and 21 CFR 210/211/820

    Deadline: February 17, 2016 | Date: February 18, 2016

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

    Updated: 2016-02-04 19:58:32 (GMT+9)

    Call For Papers - CFP

    Learn everything about Quality Management System that is common in Pharma and medical device. Sign up for this webcast today.

    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.