Learn more about recent medical device manufacturing industry trends and discover all the tools and insights you need to help you find the right QMS.
Knowledge is Power
The QMS buyer’s guide helps answer the following questions:
What are the regulatory requirements for a Medical Device QMS?
How to choose a QMS software that is designed for your company’s needs.
How to ensure a quick, smooth and effective QMS implementation?
Which capabilities of Quality 4.0 should be included in your QMS?
21 CFR Part 11 Compliance Checklist [XLS Download]
One of the main challenges across the life science industry is maintaining 21 CFR Part 11 Compliance. These particular regulations are in place to define how companies operating within the life science space use a QMS to manage electronic records and digital signatures. Although these regulations have been in place for a while, they still…
Current Good Manufacturing Practices, known as cGMP, are designed by the FDA to regulate the quality of pharmaceutical goods in the United States. With a vast array of current guidance documents to say the library is extensive is an understatement. The library includes validation, data integrity, quality metrics, and even animal and veterinary guidelines. While…
Healthcare is an enormous and lucrative industry, one which is constantly innovating and adapting. As our capabilities, technology, and culture change and evolve, so too must our healthcare institutions. Today’s patient lives in a world populated with curated content feeds, personalized shopping suggestions, and tailored ad algorithms – and they expect a similarly customized healthcare…