Purchase any WEBINAR and get
10% Off
Validity : 22nd Aug'26 to 01st Sep'26
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 ...
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 ...
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 ...
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 ...
A critical aspect of applying Agile in GMP and GCP projects is recognizing that regulatory frameworks were historically designed around linear development models, yet today’s life-science organizations operate in fast-moving environments where iterative learni ...
In today’s fast-paced and data-driven world, efficiency, accuracy, and innovation are more critical than ever. This session will introduce you to the seamless integration of ChatGPT with Excel, showing how AI can dramatically boost your spreadsheet capabilitie ...
In the tightly regulated landscape of FDA-controlled industries, successful navigation through inspections is a cornerstone of organizational success. The Most Common FDA Observations and Prevention Strategies' training addresses the critical need for professi ...
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 ...
If you work in a GMP-regulated industry, addressing human error deviations isn’t just about mitigating inconvenience—it’s a fundamental regulatory requirement. Across various GMP regulations globally, including FDA, EU, and ICH guidelines, ensuring that errors ...
Are you often tasked with managing short-term projects but don’t have formal training in project management? Tailored for professionals like managers, administrators, and operations specialists, this 50-minute session provides a straightforward approach to man ...