Central Management of Clinical Dossiers

Cardiabase's Central Management of Clinical Dossiers Service, tailored to meet the specific requirements of our clients, has contributed to the successful completion of numerous trials.

Cardiabase implements well-established and efficient processes for both paper-based and web-based international clinical trials. Quality control is assured at each step of the process and is documented through a study-specific quality control plan.

Cardiabase offers the necessary operational and technological infrastructure required to conduct and coordinate an independent review:

  • Management of assigned project team
  • On line project status reports
  • Image collection at a central location and management of the blinding process
  • Standardization of imaging
  • Query resolution
  • Writing independent review charters for approval by regulatory authorities
  • Subcontracting independent reviewers and training them on the assessment criteria and their roles and responsibilities
  • Managing the logistical processes involved in the independent review

 

Moreover we also can assist you with Investigator meeting preparation and conduct.

Cardiabase has constently exceeded our its client expectations with its high quality data managment services, leading to many long-term partnerships.
 

Key Advantages:

Although Cardiabase has developed its own internal and efficient project tracking system, it offers complete flexibility by building customized tracking tools or letting your company use its own tracking system.

Investigator meeting presentations.

Efficient document handling and archiving.
 

Cardiabase is an ECG Lab & CRO in the heart of Europe

Contact Europe : +33 (0)3 83 39 10 10  -  Contact USA : +1 860-389-5029  -  Contact by e-mail
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