Thera-Business provides expertly advised resources for you to use towards improving your literature reviews and evidence based-reports. We are experts in the development of well-written regulatory documents, and bring over 20 years of experience to you in our resources.
Smart, innovative, and fearless - our team is here to help you!
For Thera-business, high quality is not an added value, it is an essential basic requirement.
We will help you generate successful regulatory documents while building higher on evidence-based foundations.
Thera-Business has been providing medical research and writing services for over 20 years. We are experts in regulatory documents, systematic reviews and meta-analyses, post-market surveillance, and EU MDR implementation. In addition to providing the services outlined below, Thera-Business can provide scientific counsel and project management services.
Thera-Business consultants conduct objective, rigorous systematic reviews of the safety and performance of medical devices and pharmaceutical drugs/biologics. Our consultants have the education and experience to be able to rigorously appraise and analyze clinical research studies.
We offer professional medical writing services to assist with a variety of documents including manuscripts, white papers, and promotional materials. With a team of highly-trained experts, ensuring quality documentation is our highest priority.
EU MDR Implementation
Our professional consultants will work with you to ensure full compliancy with the new EU MDR regulations. Our expert team of medical researchers and writers will help you transition seamlessly.
Thera-Business assists with a variety of post-marketing surveillance activities from Post-Market Surveillance Reports to comprehensive literature reviews for risk monitoring. We offer a variety of professional services based on best practices.