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Our team is available for your project.

A team is formed first, then leads your project.

You may either entrust us with your Phase-II, -III or -IV study or choose the type of support you would like to have. Our experienceknow-how, abilities and potentials as a high-performance team is at your service.

Our in-house procedures are similar to yours or those used in major Pharma Companies, with which we work on a daily basis.

The service we are providing is as follows:

  • Clinical trials conducted in compliance with the best quality standards.
  • Rigor in terms of protocol design, study conduct and result analysis.

We know how to anticipate a problem, we think about it with you and suggest the best solutions suitable for your project.

The therapeutic areas we have successfully managed are extremely varied and all of our medical expertise is made available to you.

Our motto: « Quality at your service ».
 

    'a la carte' service


  • Project management

  • Monitoring, Screening of investigational sites

  • Documentation and CRFs  writing

  • Management of TUs and CRFs,  all dispatches

  • Management of payments and settlements (doctors, patients)

  • Submission to Authorities

  • Management of the Central  Lab

  • ICH-compliant protocol, ICF and CSR medical writing

  • Management of AEs, SAEs, Temporary Authorization for Use

  • Trial monitoring and follow up/Management of CRFs  and queries

  • Preparation of surveys

 
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