URGENT PANDEMIC INFORMATION

In light of the pandemic situation events until September 2021 are cancelled. We will inform customers directly when the events are rescheduled.    
COVID CANCELLED: Project Management in Human Resources,   Boston MA, Jan 6-8, 2021
COVID CANCELLED: InterDrone, The International Drone Conference,   Cambridge MA, Jan 11-13, 2021
COVID CANCELLED: Supplier Management for Medical Device Manufacturers,   Cambridge MA, Feb 2-4, 2021
COVID CANCELLED: US Immigration Compliance Strategies,   Boston MA, Feb 15-18, 2021
COVID CANCELLED: Project Management Training,   Boston MA, Mar 3-5, 2021
COVID CANCELLED: Internal Audit, Fraud Risk Assessment Workshop,   Boston MA, Mar 22-25, 2021
COVID CANCELLED: Agile / Scrum Training,   Boston MA, Apr 12-14, 2021
COVID CANCELLED: Validation, Verification and Transfer of Analytical Methods,   Boston MA, Apr 19-21, 2021
COVID CANCELLED: Computer System Validation - Reduce Costs and Avoid 483s,   Boston MA, May 10-12, 2021
COVID CANCELLED: SharePoint Technology Conference,   Boston MA, May 26-28, 2021
COVID CANCELLED: Employment Laws Certificate Program,   Boston MA, Jun 7-9, 2021
Following events are tentatively planned but may be rescheduled, based on CDC guidelines or attendee registration interest .    
TENTATIVE: 21 CFR Part 11 Compliance,   Boston MA, Sep 22-24, 2021
TENTATIVE: Quality Control Laboratory Compliance,   Boston MA, Oct 6-8, 2021
TENTATIVE: Analytical Instrument Qualification and System Validation,   Boston MA, Nov 15-17, 2021
TENTATIVE: FDA's New Import Program for 2021,   Boston MA, Dec 7-9, 2021

Boston Professional Events List


Batch Record Review and Product Release - 2020


Date
Oct 15, 2021 - 10:00 AM
Organizer
Netzealous LLC DBA - Compliance4All
Venue
online
Location
Netzealous LLC DBA - Compliance4All,

Fremont,
CA,
US,
ZIP: 94539
Phone: 18004479407

Ticket Price: $ 150.00
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.

Why should you Attend: 
Recognize regulatory requirements for batch records and batch record review.
Discover the essentials of batch record reviewer qualifications and training.
Establish a working relationship between production and quality reviewers. 

Areas Covered in the Session:
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.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

Event Categories
Keywords: HealthCare , medical , product




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