So join us to equip you with tools and scenarios where you can utilise the principles of QRM within your pharmaceutical operations to minimise risk and maximise success!
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.
Join this webinar to learn how many operation elements on a production site must be integrated to achieve maximum process reliability. Maintenance activities are one part of this picture, which we will explore as we discover how to improve equipment availability and product quality and reduce operating costs.
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.
Audits are a quality professional’s worst nightmare: performance review, school exam and vital professional milestone all in one. This webinar gives you everything you need to turn audits from last-minute scrambles to comfortable routines.
Join this webinar to learn how many operation elements on a production site must be integrated to achieve maximum process reliability. Maintenance activities are one part of this picture, which we will explore as we discover how to improve equipment availability and product quality and reduce operating costs.
With last year’s industry initiatives and FDA’s new CSA guidelines, regulators want life science companies to ditch paper once and for all. Join this webinar to learn how to drive a successful end-to-end paperless journey and master the milestones to a fully digital quality approach.
Learn the specific auditing requirements for the initial supplier/contractor qualification and the tools and knowledge you need to plan these audits. We will also cover what to look for throughout the process and when reviewing key documents and quality systems requirements such as SOPs, Validations, Change controls, and investigations.
In this webinar, you will gain a thorough background in all the important regulatory changes and updates that are going on right now. This will allow you to make informed choices about what regulations impact your operations and need- to- have specific regulatory actions, operational changes, and QMS updates.
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.
