Smart Quality is not just a catchphrase that will soon be trendy – it’s a revolution that will reshape what quality and service can do. This article will explain more about the Smart Quality framework and how it can help your companies move from a compliance-based culture to a quality-focused one.
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.
FDA has developed Quality Management Maturity Program (QMM) for drug manufacturers to have consistent, reliable, and robust business processes to achieve quality objectives and promote continual improvement. This article will explain the meaning of QMM and why do pharma companies need to develop a QMM program.
By attending this webinar you will understand the benefits of evolving from compliance-only solutions to the Smart Quality model.
By attending this webinar, you will get an introduction to the quality management maturity program, its rationale, desired aims, and recent developments.
The European Commission has published the long-awaited Annex 1 to the EU-GMP. The annex brings significant changes to the requirements for manufacturing sterile medicinal drugs.
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?
In this webinar, you will learn how to build good relationships and loyalty with your suppliers so that they’re easy to work with and help you produce a high-quality, compliant product.
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.
