Registry services

National Health Authorities FOPH are now frequently requesting for post-marketing registries as a condition for reimbursement of drugs or devices from the mandatory health insurance. We can support you in design of a lean solution which can satisfy both treating physicians and the authorities. We can provide you with regular reports, data summaries and analysis out of the registry. We can manage your registry project from A to Z:

  • Registry design (prototyping)
  • Registry protocols
  • Patient information documents
  • Patient registries for reimbursement purposes
  • Registries for tracking of medical devices
  • Registries for rare diseases
  • Clarify regulatory pathways for registries
  • Submission of registry projects to ethics committees and regulatory authorities
  • Training of physicians and investigators on site and remotely

Multinational clinical trials Phase I to Phase IV

Appletree CI Group offers performance of clinical trials from Phase I to phase IV…

Regulatory and Clinical Writing

Our medical writing services include the entire range of documents needed to conduct…

Biostatistics

Professional statistical analysis is an essential component in well-designed and succ…

Devices pre- & post-marketing studies

Regulatory and operational requirements for clinical investigations of medical device…

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…