Search Trainings

Search
Filter
Reset

207 results of "Life Sciences x"
Live Webinar

ChatGPT for CPAs and Finance Professionals

CPAs spend too much time on repetitive work. In this practical session, Ray shows how ChatGPT, AI, and Excel automate spreadsheet tasks, reporting, and communication. By mastering prompt skills, routine CPA and finance work becomes faster, clearer, and made ea ...

  • Basic & Intermediate
  • 90 Mins
  • Ray Evans
  • Aug 25, 2026
Live Webinar

ChatGPT and HR: A Complete Guide

How is AI evolving to influence our work in HR?  What is the role of ChatGPT as we carry out our everyday role as an HR professional?  What are the advantages of integrating ChatGPT into our work in HR?  Come laugh, listen and learn as Chris DeVany guides us t ...

Live Webinar

CoPilot for Excel

This course is designed to teach learners how to use COPILOT for Excel, a powerful tool that can help you automate tasks, analyze data, and create reports in Excel. Throughout the course, learners will explore the features and capabilities of COPILOT for Excel ...

Live Webinar

FDA's New QMSR Device Inspection Requirements

The US FDA, a has published their QMSR 21 CFR 820, to replace the previous QSR 21 CFR 820, Medical Devices, implemented February 02, 2016. They also released their new Device Inspection Manual 7382.850, on the same date, with the focus on Patient / User Risk M ...

Live Webinar

Payroll Reconciliation and Reporting – 2026 update

Payroll operations are a day to day process. From the time you decide to hire workers - from the first day of employment to the last - reporting information concerning their HR and payroll is essential to your business. Most businesses use payroll software and ...

Live Webinar

DHF (Design History File),DMR, DHR, Technical Documentation Files – US FDA and EU MDR Requirements

This webinar will examine the existing requiements for the US  FDA's DHF -- including its derivitive documents, the DMR and DHR, and the identical ISO 13485 7.3 D&DF. It will consider the EU's recently revised MDR and it's Technical Documentation File requirem ...

Live Webinar

21 CFR Part 11 - Compliance for Electronic Records and Signatures

This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA-regulated companies, and how conformance to Part 11 differs from just having good IT security. Procedures for controlling electronic signatures and electronic records as described in ...

Live Webinar

ChatGPT / AI and Project Management for FDA-Regulated Companies

This webinar will provide valuable guidance to regulated companies in development and implementation of Project Management Planning concepts including some common chatbot / AI tools (and their risks), Lean / Agile principles, for new product development, Desig ...

Live Webinar

Claude AI for HR Professionals

You Have More HR Work Than Hours in the Day. Claude Can Help — If You Use It Right. Job descriptions to write. Resumes to screen. Performance reviews to draft. Difficult conversations to plan. Manager emails to soften before they hit "send." And then leaders ...

Live Webinar

The Validation Master Plan – The Unwritten Requirements

Verification and validation requirements have always been part of the US FDA’s cGMPs. However, with increasing technology, both industry, and regulatory agencies' expectations have increased. Recent high-profile field problems indicate that V&V activities are ...

Working Hours

Mon- Fri : 8:00am - 4:00pm CDT

Quick Contact

+1-800-498-2906(US Toll free)

Contact Us

Support

Instant Discount

Purchase any WEBINAR and get

10% Off

CODE: SAVE10
T&C applicable, please referFAQ

Validity : 20th Aug'26 to 30th Aug'26