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COVID-19 Vaccination Programs & Implications
Of The Human Microbiome
Differentiators
1
Reach across the India
Integrated with various major government and private hospitals
2
Global Project Managers
Single point of contact from initiation to closing of the trial
3
Technology Integration
Electronic data capturing & Patient IWRSs
4
Rapid Start-up
Our Experienced team can provide realistic study start up timelines
5
Regional Presence
Regional associates across the India
In a Nutshell
Clinical Trial Services
Trial monitoring
- Investigator Identification and Site selection
- Site Qualification
- Site Initiation and Site staff Training
- Interim and Routine Monitoring Visits
- Ensuring subject safety and regulatory compliance
- Source data verification and CRF data review
- Monitor Adverse Event reporting
- Ensure regulatory compliance
- Close Out Visits
Project Management
- Project Plan development, Feasibility assessment, Investigator and Site selection
- Study set-up and site start up
- Organizing Investigator Meetings and Site training
- CRA resourcing, mentoring, co-monitoring support and monitoring report review
- Third party vendor management
- Managing study supplies and clinical site payments
- Managing sponsor communications
- Ensure the trial team performance is compliant with all applicable regulatory requirements, project-specific SOPs and industry best practices
- Managing client expectations for on-time and on-budget performance
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