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29 results of "Food & Dietary Supplements x"
Live Webinar

AI’s Errors May Be Impossible to Eliminate – What That Means for Its Use in the FDA

Artificial Intelligence tools are rapidly being adopted across FDA-regulated industries for activities such as quality review, document generation, audit preparation, complaint trending, pharmacovigilance analysis, validation support, and regulatory submission ...

Live Webinar

Cybersecurity - The US FDA's Requirements

Cybersecurity is the art of protecting networks, devices, and data from unauthorized access or criminal use. It is the practice of ensuring confidentiality, integrity, and availability of information. Due to the growth of the cybersecurity threat to electroni ...

Live Webinar

Compliance with 21 CFR Part 11 and AI

This webinar describes exactly what is required for compliance with Computer Software Assurance guidance, 21 CFR Part 11, and the European equivalent Annex 11 for local, and SaaS/Cloud hosted applications. It explains how to validate software employing Artific ...

Live Webinar

ChatGPT: A Comprehensive Beginner's Guide

Artificial intelligence isn’t the future—it’s here now, transforming every field from healthcare to marketing. At the heart of this shift is ChatGPT, a powerful tool helping professionals write, research, and solve problems faster than ever. Understanding how ...

Live Webinar

No-Panic Presentation Skills: How To Speak Confidently & Compellingly Anywhere, Anytime

Everyone from the anxious beginner to the confident professional will grow from expert advice such as:  Making the most of your first three minutes Reinforcing sticking points throughout your presentation Fine-tuning your eye contact, gestures and overall ...

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

How to Prepare for an OSHA Audit

An OSHA inspection provides a view into your organization’s safety culture. This training will share a step-by-step guide on how to strategically prepare for a safety audit before it happens, which includes newly defined rules that employers need to know. Addi ...

  • Basic & Intermediate
  • 60 Mins
  • Jose Mora
  • Sep 08, 2026
Live Webinar

The 6 Most Common Problems in FDA Software Validation and Verification

This training on FDA software validation and verification will provide you with the best practices necessary to ensure that all systems are validated in compliance with FDA regulations.

Live Webinar

FDA's New CSA - Computer Software Assurance Guidance

Regulated CGMP companies must develop / implement a formal CSA, Computer Software Assurance program, addressing AI where appropriate, per the FDA's recent Guidance Document. Software and related hardware design, development, verification and validation is dif ...

Live Webinar

Mastering US FDA's and EU MDR Core Medical Device Files: DHF, DMR, DHR, and Technical Documents

The FDA's DHF, DMR, DHR, and the EU's MDR TF/DD - Meeting their different purposes; future trends. This webinar will examine the existing requirements for the US  FDA's DHF -- including its derivative documents, the DMR and DHR, and the identical ISO 13485 7. ...

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Validity : 18th Jul'26 to 28th Jul'26