Arevna Consulting is a solutions provider for the Medical Device sector in Quality and Regulatory compliance for small, medium, and large device manufacturers. With over 20 years of collective industry experience in supporting manufacturers design & develop, launch products, update files and support our clients from concept of idea to registration and sales across the world.Please get in touch for more information0208 0497497

Management Consultant for Pharma, Medical Devices and the Healthcare industry. Offering:Project Management & DeliveryWorkforce Planning and ManagementManagement ConsultancyBusiness AnalysisWorking with clients & consultants across the;• Healthcare, Medical Device and Pharma sectors, Quality & Regulatory and Statisticians & Biostatisticians. SAS Programmers & Biostatisticians, Clinical Research and Operations, Clinical Trial Associate (CTA), Clinical Study Start Up / Submissions Specialist, Clinical Research Associate (CRA, CRA 2, SCRA, Lead CRA), Clinical Study Manager, Clinical Trial Manager (CTM, CTL), Project Manager / Director (CPM, CRM, CSM), Clinical Operations Manager / Director (COM, COD)