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.
By attending this webinar you will understand the benefits of evolving from compliance-only solutions to the Smart Quality model.
Gain insights into why upgrading your equipment offer greater security and enhancements to anti-counterfeiting measures, as well as some improvements in operational efficiencies.
By attending this webinar, you will get an introduction to the quality management maturity program, its rationale, desired aims, and recent developments.
Join this webinar to understand the quality culture for data integrity, diving into data integrity crucial aspects and validation as continuous improvement.
Quality-conscious life science businesses know they need quality management software to get stronger, fitter and smarter. But as they search, their options multiply and confusion mounts. What does cloud-based actually mean? Are on-premise systems really a safer bet? And how do costs compare?
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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