Regulatory Requirements for Batch Record Review
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Website https://www.compliance4all.com/control/w_product/~product_id=502234LIVE?channel=ourglocal_Dec_2018_S |
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Category Critical Processing Parameters, Batch Record Review, Production Managers
Deadline: December 01, 2018 | Date: December 03, 2018
Venue/Country: Online, U.S.A
Updated: 2018-10-08 14:37:14 (GMT+9)
Call For Papers - CFP
Overview:A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of pharmaceuticals, biologics, medical devices, etc.Areas Covered in the Session:Critical Processing ParametersSkills and Responsibilities of an Effective Batch Record ReviewerTools for Effective Batch Record ReviewEnsuring Production and Quality Reviewers Coincide with their ReviewsWho Will Benefit:Quality Assurance Batch Record ReviewersProduction PersonnelProduction Managers who Review Batch RecordsSpeaker Profile:Danielle DeLucy MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 17 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations.Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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