As regulations and their interpretation are changing so quickly we prefer to work with experts who are continually involved on the latest applications in this field. Therefore we prefer cooperation with tried and tested Regulatory Affairs consultants who are able to use their professional experience together with their knowledge. This kind of assistance perfectly meets our clients expectations, in particular small biotech companies that require more supportive guidance through the regulatory process. We provide support in assembling and preparing submission packages that are required to register a sponsored clinical trial in Poland.
