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.
Sign up for our comprehensive online on-demand GMP refresher course today and take control of your knowledge and skills in the field.
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.
By joining this webinar you will get an insight into the requirements for commercialisation and licencing to launch established products in the EU.
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 explore how companies can assess their digital quality maturity and how upgrading to a digital, connected system can provide many benefits. We will examine the latest trends in quality management systems (QMS) and document management systems (DMS) and how they can help companies streamline their operations, improve collaboration, and increase efficiency. Additionally, we will discuss the challenges companies may face when transitioning to a digital system, how to overcome them, and practical next steps.
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.
This webinar gives you the tips and common mistakes you need to consider to get a world-class and airtight life science supply chain in place.
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.
