Analytical Instrument Qualification – An introduction into reaching GMP compliance for your equipment
Do you want to launch your pharmaceutical products onto the global market? Unfortunately, this is easier said that done. Countries and their laws apply strict GxP regulations on pharmaceutical products, before they can reach your patients. In this webinar, we would like to give you and your company an introduction into GxP compliance for your analytical instruments, why GxP is required by the global market, and a guide how to obtain the required documentation to reach GxP compliance.
In this webinar, you will learn about the following subjects:
- What is Analytical Instrument Qualification?
- Why is it required?
- An introduction into the GxP regulations
- A guide on reaching compliance for your analytical instruments
- Brandon van Rosendaal – Validation & Compliance Engineer
- Stefan Swaenen – Sr. Validation & Compliance Engineer
Duration Presentation: 60 minutes (12:00 hrs. CET)
You can view this webinar from your computer, tablet or mobile phone.
About the presenters:
Stefan Swaenen has 16 years of experience in Analytical Instrument Qualification. Last 3 years he worked at Agidens on Qualification projects in diverse GMP environments and is passionate about helping our customers moving forward in the most efficient way.
Brandon van Rosendaal joined Agidens 1 year ago after he finished his Chemistry Master. He participates on lab instruments validation and process validation projects to serve our customers in the Netherlands.