RRL News – RRL are recruiting for the role of Senior Regulatory Affairs Consultant – Ireland/UK

Job Description This position is responsible for the provision of regulatory advice to clients, preparation of critical regulatory documentation, representation of Real Regulatory and client companies at meetings and management of regulatory projects.  The successful applicant will be integral to the success of clients key projects from a Regulatory perspective. This can be a full […]

Clinical Evaluation Reports

Clinical Evaluation Reports for Medical Devices and the new MEDDEV 2.7/1 (rev 4)

Need to create or update your Medical Device Clinical Evaluation Reports? Published in June 2016 by the European Commission, MEDDEV 2.7/1 ‘Clinical Evaluation: A Guide for Manufacturers and Notified Bodies Under Directives 93/42/EEC and 90/385/EEC, the new guidance document is much more explicit on how to undertake a robust and systematic clinical evaluation, and how […]

Lanuching innovation products and start-up companies with Real Regulatory guidance

Innovative Products and Start-Up Companies

Do you have an innovative product? Are you a Small or Medium Enterprise needing assistance to fully capitalise your product’s potential? The pressure on companies to raise capital and fully maximise the potential of new drug candidates is ever growing. The cost of development is ever rising and the battleground for finance is becoming increasingly […]