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Excel Spreadsheet in FDA Regulated Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance
Overview:The use of Excel in FDA-regulated environments extends beyond basic data organization and a..
Date : 19th November 2024
Time : This Event is Over
Duration : 75 Mins
Best Practices for Responding to a Form 483 Citation and/or Warning Letter Issued by FDA in 2024
Overview: The U.S. Food and Drug Administration (FDA) plays a critical role in safeguarding p..
Date : 30th August 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
An Advanced Course on Lean Documents, Lean Configuration, and Document Control in 2024
Overview: In today's fast-paced life sciences industry, many companies struggle with cumberso..
Date : 20th August 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA
10 Minutes excerpt from the recorded event for your review:Read the LinkedIn Article: LinkedIn ..
Date : 30th May 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR-
Overview: In today's rapidly evolving life sciences landscape, ensuring data integrity and pr..
Date : 21st March 2024
Time : This Event is Over
Duration : 90 Mins
Excel Spreadsheets - Step-By-Step Instructions for Ensuring Data Integrity
Overview:The use of Excel in FDA-regulated environments extends beyond basic data organization and..
Date : 29th January 2024
Time : This Event is Over
Duration : 90 Mins
Excel Spreadsheet in FDA Regulated Environment in 2023
Overview:The use of Excel in FDA-regulated environments goes beyond typical data organization and an..
Date : 28th September 2023
Time : This Event is Over
Duration : 90 Mins
Best Practices in Preparation for an FDA Computer System Audit in 2023
Overview:FDA requires that all computer systems used to produce, manage and report on “GxP” (GMP, ..
Date : 18th August 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Functional and System Requirements for Systems Regulated by FDA - New Updates Included
Overview: Computer System Validation (CSV) has been regulated by FDA for more than 35 years, a..
Date : 28th June 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Water Systems in Pharmaceutical Manufacturing Industry
Overview: This seminar will provide an overview of water systems used for pharmaceutical manu..
Date : 22nd September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Writing Effective SOPs for the Medical Device and Pharmaceutical
Overview: Standard Operating Procedures (SOPs) are a critical ingredient in an effective and ef..
Date : 30th June 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Effective Pharmaceutical GMP Audits and Self-Inspections
Overview: Because of the extreme criticality of GMP audits and the potential consequences, man..
Date : 24th February 2022
Time : This Event is Over and the Recorded Copy is Available
Duration : 60 Mins
Writing Effective SOPs for the Medical Device and Pharmaceutical
Overview: Standard Operating Procedures (SOPs) are a critical ingredient in an effective and ..
Date : 18th November 2021
Time : This Event is Over and the Recorded Copy is Available
Duration : 1 Hour 02 Mins
Sterilization of Pharmaceutical Products and Medical Devices
Overview: This topic will discuss the methods of sterilization to be used on medical devices a..
Date : 19th August 2021
Time : This Event is Over and the Recorded Copy is Available
Duration : 60 Mins
Functional and System Requirements for Systems Regulated by FDA in 2024
Overview: The validation of computer systems (CSV) under FDA regulations has shaped the way e..
Date : 25th November 2024
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 90 Mins