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Stay updated on latest GMP trends through our webinars and articles

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Guidelines for Creating a Top-Notch Mapping Protocol for GMP and GDP

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.

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How to Be Constantly Audit-Ready

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.

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What Does It Take To Build an Effective Maintenance and Reliability Organization?

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.

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How to Make Your Quality Management System 100% Paperless

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.

E-Signatures in Pharma: Challenges, Solutions, and Best Practices

E-Signatures in Pharma: Challenges, Solutions, and Best Practices

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.

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Quality Systems in the Digital Era: Are You Ready for the Future?

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.

Important GMP Regulatory Intelligence Digest for 2022/23

Important GMP Regulatory Intelligence Digest for 2022/23

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.

Do You Want To stay updated on latest GMP and pharma trends?

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Wait, don't leave empty-handed!​

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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