GMP Webinars & courses for pharma professionals

This webinar will give you an understanding of the purpose of performing a System Risk Analysis (SRA) and its benefits over other risk assessment techniques. ...

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. ...

Gain in-depth knowledge of what to consider when setting up an audit program within a GDP or GMP environment, specifically about factoring in risk analysis methodologies. In addition to understanding ‘what’ is important, participants will understand precisely ‘why’ this is important, why we must consider the wider risk element and why reducing its overall impact is critical to its success. ...

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. ...

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. ...

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. ...