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Regulatory Requirements for Batch Record Review

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Website | Edit Freely

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


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 Parameters

Skills and Responsibilities of an Effective Batch Record Reviewer

Tools for Effective Batch Record Review

Ensuring Production and Quality Reviewers Coincide with their Reviews

Who Will Benefit:

Quality Assurance Batch Record Reviewers

Production Personnel

Production Managers who Review Batch Records

Speaker 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$150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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