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Effective Technical Writing for Medical Devices: Improving Your Skills for Clear and Concise Communication
Overview: In the world of medical device manufacturing, technical writing is more than just a..
Date : 27th March 2025
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 in 2025
Overview: In today's rapidly evolving life sciences landscape, ensuring data integrity and priv..
Date : 14th February 2025
Time : This Event is Over
Duration : 90 Mins
Payroll Documentation and How to Build a Good SOP
Overview: In an era where streamlined processes and strategic foresight are paramount, this w..
Date : 02nd February 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 75 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
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
Clinical Trial Systems: Trial Master File (TMF) and eTMF, & FDA’s Recent Draft Guidance for Electronic Records/Signatures Used in Clinical Trials
Overview: Organizations involved in the conduct of human clinical trials must meet rigorous re..
Date : 30th September 2025
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 90 Mins