Recorded Webinars
Explore a wealth of knowledge at your own pace with Amorit Education's recorded webinars. Click to access an extensive library of recent and past sessions across diverse industries. Make a purchase and receive the download link via email almost instantaneously, allowing you to dive into expert-led content whenever, wherever suits you best.
Nacha Rules Changes and Updates for 2022 and the Future
Overview: Each participant in the ACH Network is required to follow the Nacha Operating Rules ..
Date : 28th November 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Preparing a FDA 510(k) submission - What to Know
Level:- Beginner to Intermediate Overview: Preparing a submission to get FDA approval for ..
Date : 22nd November 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
510K Submission Process for Medical Devices
Level:- Beginner to Intermediate Overview: There are three types of 510(k) submissions t..
Date : 21st November 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Clinical Trial Master File (TMF) and electronic Clinical Trial Master File (eTMF) and FDA Compliance
Overview: Companies engaged in the conduct of human clinical trials must adhere to specific g..
Date : 28th October 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
ABC’s of Completing the Annual ACH Rules Compliance Audit
Overview: The Nacha Operating Rules and Guidelines require that all participating depository ..
Date : 27th October 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Simplifying the Complexities of the Family and Medical Leave Act
Overview: The Family and Medical Leave Act is probably THE most complex piece of federal empl..
Date : 26th October 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Medical Device Software Validation Meeting FDA Regulations
Overview: Testing software to prove that it works and has no bugs is not sufficient to obtain ..
Date : 25th October 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
NEW Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities
Overview:Recent updates to the Nacha Operating Rules are further clarifying the Roles and Responsibi..
Date : 30th September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Unemployment Insurance – 2022 - 2023 Critical Issues
Overview: Unlike other human resource management issues, unemployment insurance (UI) managemen..
Date : 28th September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Data Integrity and Governance for Computer Systems Regulated by FDA
Overview:The Webinar will focus on the importance of ensuring that the validation of an FDA-regulate..
Date : 27th September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Multi-State Payroll Taxation - Understanding the Payroll Laws in Each State
Overview: To better understand the laws in each state and the tax guidance on how to determine ..
Date : 27th September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Human Factors/ Usability Studies following ISO 62366 and the new FDA Guidance
Overview: Human Factors/ Usability is the analysis of how people interact with medical devices...
Date : 23rd September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 60 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
Excel Spreadsheets in FDA Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance
Overview: This interactive webinar explains how to configure and validate a GxP compliant sprea..
Date : 15th September 2022
Time : This Event is Over
Duration : 90 Mins
Pharma 4.0 - Overcoming Data Integrity Issues in the Cloud to Meet FDA Compliance Requirements
Overview: Computer system validation has been regulated by FDA for more than 30 years, as it ..
Date : 31st August 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 1 Hour 40 Mins