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25/04/2017
“The Benelux Pharmacovigilance Day 2016”.

Come and join us at “The Benelux Pharmacovigilance Day 2016” on October 11, 2016, in Amsterdam....

25/04/2017
"Risk minimization in data anonymization process"

Come and join us in Barcelona for the 2016 PhUse annual conference. ...

25/04/2017
KeyrusBiopharma is going to be present on the “BCF Career Event Belgium”.

KeyrusBiopharma is going to be present on the “BCF Career Event Belgium”....

25/04/2017
DII 3rd annual conference on

DII 3rd annual conference on "Health data revolution"...

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Our Know-How

Feasibility and Project Management

Our Project Managers and Clinical Research Associates manage every step of your national or international projects.

They ensure that the research is compliant with Good Clinical Practice, ICH recommendations and local laws and regulations.

They will use your or our own Standard Operating Procedures as requested for the following services.

Project Management

  • Feasibility studies in France and abroad
  • Regulatory submissions (ethics committees and competent authorities)
  • Identifying potential investigational centres (phase I, hospital, doctor’s surgery)
  • Evaluation of the overall budget per investigator or activity centre
  • Estimation of timelines
  • Writing of the specifications manual
  • Management of confidentiality agreements, contracts, hospital agreements and extra costs
  • Writing of the consent form, patient's diary ...
  • Case report form (CRF) design
  • Creation of study documents (essential and regulatory documents, investigator file, trial master file...)
  • Management and logistics of the study materials (products, biological kits ...) and study documents (printing, mailing ...)
  • Management of invoices and investigators’ fees
  • Communication: organisation of meetings (Investigator, CRA), newsletters
  • Coordination of the different contributors to the project (central laboratory, data management, IVRS, biostatistics, medical writing etc.)
  • Regular reporting to the client

Monitoring

  • Selection of Investigator centres
  • Creation of monitoring tools and status tables (regulatory documents, recruitment, monitoring visits, adverse events, etc.)
  • Initiation, monitoring and close-out visits and preparation of visit reports in French or English
  • Management of serious adverse events (SAEs)
  • Query management
  • Contact with the Investigator site teams (hospital unit, pharmacy, local laboratory)