Regulatory affairs is a fundamental part of the life science industry, with critical importance in bringing new products to the market and maintaining licences over their lifecycle. At Next Phase, we support all aspects of the life science regulatory affairs function, from new pipeline development, submissions and approvals, lifecycle maintenance, labelling & artwork, CMC, regulatory operations as well as CE marking and 510k. Our dedicated regulatory affairs consultants work with Pharmaceutical, Biotech and Medical device clients across Europe, focusing on providing highly-skilled and talented regulatory professionals.
Below you will see our current job opportunities within this area, together with the latest industry news. You will also see the details of the Next Phase consultants who specialise in this field. Please call us on 01403 216216 to discuss how we can help you.