Upcoming Webinar

Part 2 - NEW Nacha Operating Rules Changes for 2026 and Beyond: IAT Entries, ACH Contact Registry & R90

Part 2 - NEW Nacha Operating Rules Changes for 2026 and Beyond: IAT Entries, ACH Contact Registry & R90

Overview: Each participant in the ACH Network is required to follow the Nacha Operating Rules ..

Date : 18th February 2026

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 120 Mins

Overtime, Exemptions & Salary Thresholds under FLSA (2026)

Overtime, Exemptions & Salary Thresholds under FLSA (2026)

Overview: In 2026, overtime and exemption decisions have become a moving target for payroll a..

Date : 18th February 2026

Time : 2:00 PM Eastern Time / 11:00 AM Pacific Time

Duration : 60 Mins

ISO 13485:2016 Utilizing Principles of Lean Documents and Lean Configuration

ISO 13485:2016 Utilizing Principles of Lean Documents and Lean Configuration

Overview: Medical device and life science organizations are expected to maintain a Quality Ma..

Date : 20th February 2026

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 90 Mins

Prepare for FDA QMSR Inspections: 483 & Warning Letter Response

Prepare for FDA QMSR Inspections: 483 & Warning Letter Response

Overview: FDA inspections under the new QMSR can look and feel different—not just in what inv..

Date : 23rd February 2026

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 60 Mins

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2026

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2026

Overview: In 2026, data integrity and privacy risks don’t sit in one department—they show up ..

Date : 24th February 2026

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 90 Mins

Charles H. Paul


510K Submission Process for Medical Devices

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

510K Submission Process for Medical Devices

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

Preventing Human Error in the Life Sciences - Pharmaceutical and Medical Device

Preventing Human Error in the Life Sciences - Pharmaceutical and Medical Device

Overview: Human Error occurs in all settings.  In the world of pharmaceutical and medica..

Date : 29th July 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

Preventing Medical Device Recalls – A Prevention Strategy

Preventing Medical Device Recalls – A Prevention Strategy

Overview:  In a recent study, the FDA has reported a 95% increase in medical device recalls ..

Date : 28th June 2022

Time : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

Preparing for an FDA Audit? Learn the Best Behavior Practices and the Do’s and Don’ts

Preparing for an FDA Audit? Learn the Best Behavior Practices and the Do’s and Don’ts

Overview: This webinar will begin by discussing and emphasizing the importance of truthfulness..

Date : 20th May 2022

Time : This Event is Over

Duration : 75 Mins

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