EU regulations and GXP requirements are constantly being revised while pharma and health care companies are expected to keep up with these developments. Where applicable organizations should timely implement appropriate measures to comply with these new requirements. Van Loosbroek Farma Consult can assist to proactively and effectively manage these hurdles by providing advice in relation to the interpretation and application/implementation of regulations or performing a gap assessment against specific standard(s).
Van Loosbroek Farma Consult can also be of assistance to companies who face (or are close to) a issues with the responsible Inspectorate. As a result of our experience and expertise we can assist companies to systematically resolve identified issues to the satisfaction of the Inspectorate.