Compliance with EU rules and standards (EU Acquis Communautaire) is a demanding and long-term task. Working with our experienced experts will make this process much easier.
We help countries that are approaching the EU by drafting laws and by-laws specific to medicinal products and medical devices, taking care of national requirements.
We organise and perform seminars and trainings tailored to competent authorities.
We help competent authorities interface with the EU via institutional building, strategic planning, informed decisions and quality management.
We have already implemented 21 projects across eight different countries.