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Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR-

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

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

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

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

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

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

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

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

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

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

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