Solutions

We tailor every project to your wishes and needs. You can choose an "All-round Carefree Package" or we support you as needed in case of:

  • Observational studies (AWB, NIS)
  • Clinical Trials (especially phase III and IV)
  • Clinical Trials for medical devices
  • PMCF studies
  • Investigator Initiated Trails (IIT) / Studies (IIS)
  • Epidemiological studies
  • Cohort studies
  • Register
  • PAES & PASS
  • Surveys
  • Or comparable projects

We conduct your project in conventional, electronic or hybrid form as requested. Learn more about the advantages and disadvantages of each form in the subtopic „Paper vs. eCRF“.

For more than 22 years INPADS has been assisting customers from the fields of pharmaceuticals, biotechnology, medical devices and research and development with design, implementation, evaluation of clinical studies at home and abroad.

  • Clinical trails for the evaluation of efficacy and safety of pharmaceuticals, during and after market access. Especially phase III studies, phase IV studies and non-commercial studies. These are subject to stringent and continually changing legislative, regulatory and ethical requirements.
  • Non interventional studies with pharmaceuticals are used as evidence of benefit and are of great importance for the eligibility for reimbursement of the products. Long-term post-market observations under routine conditions are capable of gaining important knowledge and securing the position in the market.
  • Clinical trails with medical devices of all classes in the course of the conformity assessment or the extension of the intended purpose.
  • PMCF studies with medical devices of all classes as post-market surveillance.