Proper Medical Writing
Europe and worldwide.
Proper Medical Writing is a regulatory medical writing consultancy and clinical research organisation (CRO) founded in 2009, with a firm position in the Central European market. The company prides itself in a high intellectual capital, expertise, and experience resulting in excellent quality of its services.
Areas of regulatory/reimbursement support:
Documentation for Medical Device registration (CE, FDA), ISO 13485:2016, Quality Management System.
Clinical evaluation report.
Clinical study design.
Clinical study documentation.
Clinical study organisation.
Regulatory and clinical trial consultancy.