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 »
Learn the language “tools” and insights that will help you ensure that quality is embraced from top to bottom throughout your organization
In this GMP training webinar, you will learn how to process corrective and preventive actions (CAPAs) effectively and maintain an efficient continual improvement system.
A free webinar that will help you change your mindset on the importance of handling correctly issues that arise during your product’s lifecycle.
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.
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