With 15+ years experience MEDLOFT is your global regulatory and quality partner. Focused in medical devices and in-vitro diagnostics, we provide you on time services to bring your devices on the market.
With the latest revisions, the medical device regulations are becoming increasingly difficult. All regulators within the developed countries are trying to have safe devices within their market. Patient safety and compliance to regulatory requirements constitute the basis of our policy. Our customer focused team provides effective and fast services for each type of the project.
MEDLOFT has a strong international team having Notified Body experience. Our staff, with technical, regulatory quality and clinical competence will provide you tailored solutions, whether you are a small start-up company or a competent medical devices manufacturer which aims to put new devices on the medical device market.
In short, MEDLOFT provides regulatory and quality solutions that accelerate the success of medical device companies to bring their products on the market.
If you want to comply with the revised regulations, have an effective quality management system for your product realization processes or to have your design reviewed for specific technical standards just contact our expert team. We will analyse your needs and provide you an effective quotation for your project.