Clinical Research and Data Management

Stratgurus caters high quality services to the Pharmaceutical Industry specifically with the CRO services acquired from variety of locations worldwide. Based on the needs, Stratgurus takes in a broad range of activities and offers a fully integrated package to meet your clinical development needs from 'Protocol and CRF Design' to the 'Biometrics' needed, from follow up and monitoring of the 'Clinical Research'  to the 'Data Management 'and Medical Report Writing. You can allocate all tasks to our teams to be completed within tight schedules and/or budgets.

We selected our partners carefully to bring only the best to the region. All our CRO partners are approved by different international regulatory authorities such as the EMEA, MHRA, US FDA, DCGI, MoH Turkey, MoH Malaysia, TFDA and BFAD.

Our experienced CRAs with diverse backgrounds are trained to international standards and are available to take part in projects at any given global location.

We Offer:

  • Bioequivalence and Bioavailability Studies
  • Data Management
  • Biometric Analysis and Clinical Writing
  • Essential Document Development and Associated Activities
  • Protocol and CRF Design (Phase III & IV Clinical Trials)
  • Electronic CRFs
  • Monitoring