ProColl Achieves ISO 13485:2016 Medical Devices Quality Management System Compliance with UKAS Accreditation
ProColl has received certification from URS for their ISO 13485:2016 quality management system, with accreditation from the United Kingdom Accreditation Service (UKAS) for the scope of manufacture of ProColl’s bovine and recombinant collagen products. ISO 13485:2016 is the medical industry’s primary medical device quality management system standard that ensures compliance with regulatory and customer needs.
The award recognises the high standard of ProColl’s systems, processes and practices ensuring the safety and quality of the company’s collagen products.
About ProColl: ProColl manufactures recombinant human collagen and bovine collagen at scale for customers in the research, medical, food and aesthetics industries. This certification adds to the list of company achievements this year including the establishment of food-grade manufacturing and receipt of grant funding from Innovate UK to support its development of type II and type III recombinant human collagen products, due for market release in the new year.
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