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    Online Training by Compliance4all on Market Corrections in Compliance with FDA

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    Website http://www.compliance4all.com/control/w_product/~product_id=501094LIVE?channel=mailer&camp=Webinar&A | Want to Edit it Edit Freely

    Category Sales/Marketing Management, Senior and mid-level Management, Quality System Auditors

    Deadline: January 17, 2017 | Date: January 18, 2017

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

    Updated: 2016-11-09 14:10:15 (GMT+9)

    Call For Papers - CFP

    Overview:

    To satisfy QSR and ISO 13485 requirements, medical device companies must respond to field reports swiftly and compliantly.

    There are certain circumstances in which a report from the field requires the device manufacturer to take steps regarding product in the field.

    Why should you attend:

    There are certain circumstances in which a report from the field requires the device manufacturer to take steps regarding product in the field. It is critical that the company take the required steps in the required timeframes. If not, FDA's sanctions could be so onerous as to result in the company's inability to ship product.

    Areas Covered in the Session:

    Regulatory definitions of recalls, removals, and market corrections

    Instances which require recalls, removals, or market corrections

    What to do during recalls, removals, and market corrections

    Recordkeeping requirements for recalls, removals, and market corrections

    ISO 13485-specific requirements

    Who Will Benefit:

    This webinar will provide valuable assistance to all regulated companies, since personnel training is a regulatory requirement in the Medical Device field. The employees who will benefit include:

    Regulatory Management

    Quality Assurance Professionals

    Consultants

    Speaker Profile:

    Jeff Kasoff , RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy and colonoscopy devices, where he oversees the operation of the quality system. In this position, Jeff is responsible for oversight of the document control system, including maintenance of regulatory documentation.

    Contact Detail:

    Compliance4All DBA NetZealous,

    Phone: +1-800-447-9407

    Email: supportatcompliance4All.com

    http://www.compliance4all.com/

    Event Link : http://www.compliance4all.com/control/w_product/~product_id=501094LIVE?channel=mailer&camp=Webinar&AdGroup=ourglocal_Jan_2017_SEO

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    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.