All clinical trials or health-related project needs people with experience and knowledge to move the process forward in a timely manner. At LINK Medical you will meet people with insight into the clinical environment – and people with the ability to create relations with key opinion leaders, hospital staff and your own organisation.
LINK Medical has based on the company´s nearly 20 years of experience created a precisely defined project work process, the LINKplan™. This process includes all the steps needed to plan, initiate, conduct, analyse and evaluate our projects. Our platform and strong presence throughout the Nordic region makes us an ideal business partner for national as well as international clinical or regulatory projects.
Having the support of an experienced and dedicated Regulatory affairs team is the key in all steps of product development. We are now expanding our regulatory department making sure that we always have an expert with the local knowledge required for successful product development in your country. Our team of 18 regulatory experts provides you with the experience, ability and integrity to support the development of you medicinal product or medical device.
Our team of Health economists have the local experience to fulfil regulatory demands and to develop health economic models for reimbursement application needed for the commercialisation of you product.
Don’t hesitate to give us a call or send us an e-mail if you want to know more about LINK Medical and our services.
LINK Medical Research
Tel.: +47 22 58 90 00