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42 results of "Manufacturing x"
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

Performance of Root Cause Analysis, CAPA, and Effectiveness Checks

This comprehensive course offers essential knowledge and practical skills in root cause analysis, corrective and preventive actions (CAPA), and conducting effectiveness checks. Participants will learn systematic approaches to identify root causes, develop effe ...

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

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. ...

Live Webinar

ChatGPT & AI for Sales and Marketing Professionals

Every successful sales and marketing team relies on effective communication, strong customer relationships, compelling content, and the ability to respond quickly to changing business needs. As Artificial Intelligence continues to evolve, organisations are dis ...

Live Webinar

Human Factors and Human Error Prevention (HEP)

How to develop, modify and use the tools of the User/Patient Device Risk Management File per ISO 14971:2019 (a major requirement of the new QMSR), Pharma's ICH Q9, and Error Reduction with IEC 62366-1, Useability Engineering, with added HEP considerations. Ex ...

Recorded Webinar

FDA Regulation of Artificial Intelligence/ Machine Learning

AI/ ML will revolutionize medicine by making diagnosis and treatment more accessible and more effective. FDA has regulated medical device software by means of regulation and guidance for years, however, AI/ML programs fall outside the scope of these regulation ...

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Validity : 19th Jul'26 to 29th Jul'26