Clinical Monitoring

Well-educated and experienced CRAs is a key to successful conduct of a study.
We provide you with the qualified CRA team to monitor protocol compliance and data integrity.
With CLAUSE your trial will be under the strict monitoring to receive the high quality data!

  • Clinical Monitoring
    • Site selection, initiation, and routine monitoring including, source data verification, site file review and drug accountability management
    • Review of eligibility of subjects
    • Essential document collection
    • Site inspection preparation
    • Status overview and subject recruitment
    • Query management and site support in problem solving
    • Site close-out activities

Please feel free to contact us anytime for more information!

CLAUSE’s team is at your service:

  • Start-up Services
  • Regulatory affairs
  • Project Management
  • Clinical Monitoring
  • Quality Assurance / Management
  • Data management services

News and events

Clause will participate in Arabian Health
24.01.2017
Clause will participate in Arabian Health

News
21.09.2016
CLAUSE Ltd, the leading contract research organization in Europe is pleased to announce the opening of a new branch office in Praha, Czech Republic.

Сontacts

We will be glad to cooperate

Feel free to contact us for any questions using any convinient way for you!

Tel +38 095 596 0666; +38 057 751 66 99

e-mail: office@clause-audit.com

Address: 20V, Kul'tury str., off.19

Kharkiv ,61058,Ukraine

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