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Medical Device Cybersecurity following September 2023 FDA Premarket Guidance
Overview: This webinar will cover FDA's evolving position on medical device cybersecurity. The..
Date : 29th November 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Annual ACH Rules Compliance Audit Webinar: Navigating New Regulations
Overview: Keeping up with annual ACH Rules Compliance Audits is mandatory for various financia..
Date : 16th November 2023
Time : This Event is Over and the Recorded Content is Available
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
How to Conduct an ACH Risk Assessment and Develop an Effective Risk Management Program
Overview:Whether you're a Financial Institution, Third-Party Service Provider (TPSP), or Third-Par..
Date : 27th September 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
RISK MANAGEMENT FOR ML MEDICAL DEVICES FOLLOWING BS/AAMI 34971 AND ISO 14971
Overview:In the field of medical technology, the integration of Machine Learning (ML) within medic..
Date : 28th August 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
510K Submission Process for Medical Devices
Overview: There are three types of 510(k) submissions that can be submitted – Traditional, Spec..
Date : 25th August 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 75 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
I-9 Form Changes: Remote Flexibility Ends, Employers Must Act by August 2023
Overview: On May 11, 2023 the President determined that the Covid-19 pandemic was no longer a..
Date : 15th August 2023
Time : This Event is Over and the Recorded Content is Available
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 ..
Date : 27th July 2023
Time : This Event is Over
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
EEO-1 Reporting Deadline Established For 2023! Prepare for Compliance!
Overview: The EEO-1 reporting deadline has become a moving target, so covered employers need ..
Date : 20th June 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Medical Device Cybersecurity following 2022 FDA Premarket Guidance
Overview: In this informative webinar, we delve into the critical field of medical device cyb..
Date : 20th June 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Engineering Change Control in Medical Device Environment
Overview:Change control focuses on managing changes throughout a product’s life cycle as a part of ..
Date : 30th March 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Good Documentation Practices to Support FDA Computer System Validation
Overview: Computer system validation has been regulated by FDA for more than 30 years, as it ..
Date : 29th March 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Best Practices for Responding to a Form 483 Citation and/or Warning Letter Issued by FDA
Overview: FDA has substantial authority to oversee regulated companies and their operations.&n..
Date : 30th November 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins