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Live Webinar Electronic Records & Electronic Signatures; 21 CFR Part 11; Basic Concepts


Date
Feb 08, 2021 - 03:00 PM - Feb 09, 03:00 PM
Organizer
WCS
Venue
online
Location
WCS Consulting Inc.3190 Stirling Rd, Unit K4 ,Hollywood, FL 33021,

Hollywood,
Florida,
US,
ZIP: 33021
Phone: 844-267-7299 | 954-947-5671

Overview

With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records. After several years of development and industry comments, 21 CFR Part11, the Electronic Records & Electronic Signatures Rule became law in 1997. Interestingly, as time passed other international regulatory agencies adopted similar e-records/e-signature regulations. Today, more than 15 years after introduction, compliance with the requirements of Part 11 (as the regulation is now commonly referred to) continues to challenge the industry. As with any regulation, understanding the basic requirements is key to achieving compliance.

This presentation will provide an overview and historical perspective of the Part 11 regulation, the general Part 11 requirements, electronic records requirements and electronic signatures requirements.


 

Why should you attend

Documented Part 11 training, as with any FDA regulation, is required for staff members who have responsibilities within the scope of the regulation. Understanding the requirements of Part 11 is critical to compliance with the regulation. Knowledge of regulatory requirements is an exercise in efficiency...both efficiency in project management and avoidance of noncompliance penalties.


 

Session Highlights

  • History and Overview

  • Subpart A: General Provisions

  • Subpart B: Electronic Records

  • Subpart C: Electronic Signatures

  • Scope & Application Guidance

  • Questions and Answers


     

Who Wil Benefit

  • Project/Strategic Management

  • Quality Assurance Staff

  • IT Staff

  • Operations Staff



Speaker Details


Speaker Profile

Carolyn Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries. 

Event Categories
Keywords: pharmaceutical




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