Jreg Consultancy Ltd

JReg Consultancy Ltd is a team of experienced professionals offering a broad spectrum of regulatory, clinical and quality compliance services. We assist both domestic and global companies in obtaining the necessary approvals and certifications to place and keep your medical device product on the market. Highly experienced Regulatory Affairs, Clinical and QMS Consulting and Training Services for Medical Device Industry. 🩻🩺🦠🧪 MDR, IVDR, UKCA, FDA 510(k), ISO 13485, CERs, Risk Assessments, Technical Documentation, PMS, PMCF, Usability, Biocompatibility, Audits, Training. Representation Services: EUAR, UKRP Gap assessments, strategies, remediation, implementation, ad hoc queries, short projects and/or fixed term support as a regulatory partner. Members of Team PRRC, RAPs and ABHI. Highly qualified consultants that undergo continuous professional development and invest in latest training. JReg only work with trusted consultants and subject matter expert partners.