The regulatory environments within the industry continue to change and vary internationally. Our regulatory and medical professionals keep track of the changes and anticipate developments globally.
We provide expertise either as an independent team or working alongside the client’s own management from early stage research through to product launch.
Chiltern’s contribution to projects can range from the strategic planning of critical paths to applying for clinical trial and marketing authorizations. We have extensive experience in providing due diligence programs and full pharmacovigilance services for licensed and unlicensed products.
The knowledge base within Chiltern’s Regulatory and Medical Affairs Team ensures that studies have consistent high standards of scientific and medical representation to meet the requirements of the relevant competent authorities. Customized seminars are also available to provide valuable training to client in-house teams.
For more information about our capabilities, please click on the links below.