MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

Regulatory Requirements for Batch Record Review

Event Details

Regulatory Requirements for Batch Record Review

Time: December 3, 2018 from 10am to 11am
Location: Online
Street: 161 Mission Falls Lane, Suite 216,
City/Town: Fremont
Website or Map: https://www.compliance4all.co…
Phone: Event Manager
Event Type: webinar
Organized By: Adam Fleming
Latest Activity: Oct 10, 2018

Export to Outlook or iCal (.ics)

Event Description

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 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
Email: support@compliance4All.com

Comment Wall

Comment

RSVP for Regulatory Requirements for Batch Record Review to add comments!

Join MedTech I.Q.

Attending (1)

© 2020   Created by CC-Conrad Clyburn-MedForeSight.   Powered by

Badges  |  Report an Issue  |  Terms of Service