Undoubtedly, the vast majority of us have sat through monthly, quarterly, and annual presentations of “Quality Metrics,” only to get to the end and wonder, “So what do we do now with all of that information? How do we improve on where we are?”, just before the meeting moves on to something else with no …
Quality Metrics in the GMP environment – Why and How? Read More »
Learn how to communicate about Quality across your organization. Talking about Quality and convincing people it matters have to be hard!
Learn about the advantages and the tools for doing a thorough gap analysis when there is a significant change to review the QMS against the new regulation.
In this webinar, you’ll learn about Product Inspection solutions that can increase quality assurance and make compliance easier.
Join this webinar for actionable takeaways to strengthen your risk and opportunity management, from grasping the fundamentals to building a risk-based culture of continuous quality improvement.
Join this webinar to learn from other companies about alternatives ways to acquire information from your suppliers and improve your auditing processes.
Learn to understand the fundamentals of thermal validation. This webinar will also provide examples of practical implementation of the different elements, ensuring you comply with the regulatory requirements.
Many pharma companies are slow to adopt newer technologies and have a legacy of paper-based systems. Consequently, maintaining compliance with evolving GMP regulations is becoming extremely challenging. For this reason, any pharma and medical device manufacturer must implement an Electronic Quality Management System (eQMS) as soon as possible. However, if not approached correctly, the …
In this webinar, you will gain a good understanding and guidance on creating a systematic intelligence and research process into the ever-changing cGMP, with as little cost and effort as possible. You will learn about various tools to do that- from the most simple and quick solutions to advanced strategies.
Many pharma and medical device professionals lack a structured and repeatable process for risk assessments. Instead, they carry out risk assessments in a patchy and irregular manner, using FMEA as a default tool. Risk Management is not only a set of tools; it is also an opportunity for process improvement. A structured, repeatable process that …
How to Pick the Right Tools for a Successful Risk Management Read More »
Download our free Ultimate FMEA Guide, which is dedicated to GMP and pharma professionals.
This extensive yet simplified guide to Failure Mode and Effects Analysis (FMEA) will help you master one of the most vital instruments in your risk management toolbox.
