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2 Days Workshop FDA Trends in Compliance and Enforcement


Date
Mar 01, 2021 - 08:30 AM - Mar 02, 08:30 AM
Organizer
WCS
Venue
Venue to be announced shortly
Location
Venue to be announced shortly Richmond , Virginia Richmond, Virginia 23173 United States,

Richmond,
Virginia,
United States,
ZIP: 23173
Phone: 844-267-7299 | 954-947-5671  

Overview

FDA requires that all computer systems used to produce, manage and report on “GxP” (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. This training will help you understand the FDA’s current thinking on computer systems that are validated and subject to inspection and audit.
As a “GxP” system, following Good Manufacturing, Laboratory and Clinical Practices, the computer system must be validated in accordance with FDA requirements. If electronic records and/or electronic signatures (ER/ES) are incorporated into the system, FDA’s CFR Part 11 guidance on ER/ES must be followed.


This workshop will focus on the key areas that are most important, including security and data integrity. Implementing and following the System Development Life Cycle (SDLC) methodology is the best approach for computer system validation and maintaining data integrity. The life cycle approach takes all aspects of validation into account throughout the life of the system and the data that it houses. The data is a key asset for any FDA-regulated company and must be protected through its entire retention period.


Why should you attend

FDA requires that all computer systems that handle data regulated by the Agency to be validated in accordance with their guidance on computerized systems. This guidance was first issued in 1983, and the main points of focus remain consistent today, despite the number of years that have passed and the technology changes that have taken place.
The guidance was revisited for its application to the medical device industry, as the first issuance addressed pharmaceuticals. In 1997, 21 CFR Part 11 was issued to address electronic records and signatures, as many laboratories and other FDA-regulated organizations began seeking ways to move into a paperless environment. This guidance has been modified over the years to make it more palatable to industry, and this includes discretionary enforcement measures. The intent was to avoid creating a huge regulatory compliance cost to industry that was initially preventing companies from embracing the technology.
This session will provide some insight into current trends in compliance and enforcement. Some are based on technology changes, and these will continue to have an impact as new innovations come into use in the industry.


 

Session Highlights

• Learn about Computer System Validation (CSV) and the System Development Life Cycle (SDLC) Methodology
• Understand “GxP” Systems
• Understand 21 CFR Part 11, Electronic Records/Electronic Signatures (ER/ES)
• Learn how Data Archival plays a key role in ensuring security, integrity and compliance
• Learn how to develop a solid Validation Strategy that will take into account the system risk assessment and system categorization (GAMP V) processes
• Learn about recent FDA findings for companies in regulated industries
• Learn about recent trends in technology that need to be addressed in the CSV approach

• Q&A

Who will benefit

Professionals in the following industries may also benefit from the content:
• Pharmaceutical
• Medical Device
• Biotechnology
• Tobacco and Related (Vapor, e-Cigarette, Cigar, etc.)
Any other FDA-regulated industry, plus any Life Science Consulting or Contracting firm
• Information technology managers and analysts
• QC/QA managers and analysts
• Clinical data managers and scientists
• Compliance managers
• Lab managers and staff
• Automation analysts
• Computer system validation specialists
• GMP training specialists
• Business stakeholders and individuals who are responsible for computer system validation planning, execution, reporting, compliance, and audit
• Consultants working in the life sciences, tobacco and related industries who are involved in computer system implementation, validation and compliance
• Anyone involved in the planning, execution, and reporting of a clinical trial (sponsor, director, researcher, regulatory role, etc.)



Agenda


AGENDA

Day One

Lecture 1: (90 Mins): 
FDA Regulatory Oversight 
Computer System Validation (CSV) 
System Development Life Cycle (SDLC) Methodology

Lecture 2: (90 Mins): 
GAMP 5 Software Categorization 
System Risk Assessment

Lecture 3: (90 Mins): 
Requirements 
Design 
Testing 
Requirements Traceability Matrix (RTM) 
Additional Validation Documentation

Lecture 4: (90 Mins): 
FDA Inspection Trends 
Regulatory Influences 
Response to Change


 

Day Two

Lecture 1: (90 Mins): 
7 Most Common Problems with Validation

Lecture 2: (90 Mins): 
21 CFR Part 11 Compliance (Electronic Records/Electronic Signatures)

Lecture 3: (90 Mins): 
FDA Audit Preparation


Lecture 4: (90 Mins):

Best Practices 
Wrap-Up
Q&A



Speaker Details


Faculty

Carolyn Troiano has more than 35 years of experience in computer system validation in the pharmaceutical, medical device, animal health and other FDA-regulated industries. 

Wcs Seminars
Registration Details
(Contact us : 844-267-7299 | 954-947-5671  
Don't wait. Register TODAY or  Email  US [email protected]
 

Event Categories
Keywords: pharmaceutical




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