Regulatory medical devices
Medical devices regulations in Europe differ from regulations for medicinal products…
Regulatory affairs
Our international Expertise for your support
We offer a wide range of regulatory services for drugs and medical devices. With our experienced team in drugs as well as in medical devices, we offer tailored solutions according to your needs.
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Orphan drug and pediatric procedures
The designation of an orphan drug is a challenging process….
Document management
We can help our clients set up and configure their document management system, tailor…
Clinical trial authorizations Europe
Appletree CI Group offers clinical trial authorization services all over Europe…
Consulting
As a full service clinical CSO, we are familiar with all aspects of clinical developm…
Legal representation Switzerland and EU
According to the regulations, Sponsors without legal residence in the EU or Switzerla…
QA/QC
Our quality assurance and quality control processes ensure adherence of our operation…
