I’m very excited to announce Propel’s newest solution for the life sciences industry! Older PLM solutions typically focus on engineering and quality. Propel does that and more. Our cloud PLM helps life sciences companies with their digital transformation. How? We offer a modern and validated cloud PLM software that can extend collaboration across an entire company, while still helping companies ensure product quality and regulatory compliance.
A key part of our announcement is the general availability of our Medical Validation Pack (MVP) for the life sciences industry. The Propel MVP offers pre-configured, out-of-the-box best practices to help life sciences companies build in product and process quality using Propel’s cloud PLM system. The Propel MVP is a complete set of validation document templates that enable customers to significantly reduce validation time and costs when deploying Propel’s cloud PLM software. Propel customers can more easily adhere to regulatory standards like ISO 13485, FDA Total Product Life Cycle (TPLC), 21 CFR Part 11 and 21 CFR Part 820.
Don’t just listen to us. Here’s what our customers have to say: “Propel’s Part 11 compliant PLM solution can help life sciences companies like R2 Dermatologycollaborate better and bring high quality medical devices to market faster,” according to Bijesh Chandran, Senior Director of Regulatory Affairs and Quality Assurance at R2. “R2’s vision is to become the most admired company in dermatology in the minds of our customers and their patients, our commercial partners, our clinical advisors, our stakeholders, and our employees. Propel’s validated PLM solution plays a key role towards R2 realizing that vision.”
As I mentioned, you can see a brief demonstration of our solution for life sciences companies. Or just sign up for our live webinar on September 14. To find out more about Propel for life sciences, visit propelPLM.com.