Join us to learn about validation specialists’ role in ensuring product quality and regulatory compliance in the pharmaceutical and biotech industries. Discover the latest trends and best practices in validation processes, network with like-minded professionals, and engage in interactive discussions.
Join us to learn the different elements you should take into account when selecting the type of calibration and choosing calibration points, as well as the uncertainties related to calibration and measurement of environmental parameters in a GxP storage environment.
This webinar discusses the importance of creating a robust temperature mapping protocol for a successful mapping exercise. Validation experts will provide insights into developing a protocol suitable for specific needs, covering the essential elements, what not to include, and common errors and lackings of protocols.
Learn about the different eSignature solutions available and the benefits and challenges they can present to users, QA, and Regulators. You will also gain practical considerations and insights to help choose, implement and audit the solutions and vendors.
This webinar will help you to take a closer look at what can and will go wrong when performing a validation test. You will also learn all the necessary tips and tricks to minimize the risks when conducting thermal validation.
In this webinar, you will learn what is temperature mapping and why it is important. How to determine sensor locations and how many to use.
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.
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.
