Learn how to ensure a successful, quick, and cost effective QMS deployment. This white paper describes how pioneering pharma companies are approaching digital transformation differently. Read how they are taking a holistic approach that hyper-scales the power of data and analytics to quickly automate and streamline processes.
Download now to learn:
Why it is critical to address quality and compliance projects not only from a technical perspective, but also a business perspective that evaluates an organization’s business needs and assumptions.
The common mistakes pharmaceutical companies must avoid when automating quality and compliance processes.
How new technologies can deliver a speedy and cost effective quality management system (QMS) deployment.
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…