Client Services
Criterium prides itself on providing personalized, high-quality,
schedule-compliant, and cost-effective services to its clients. The
involvement of our management does not stop when the contract is signed;
our senior managers and business development
teams are available to clients 24/7. This access allows for very rapid
decision-making.
Criterium has experience with a wide variety of clinical
trial project stakeholders at all levels and across various types
of organizations. Each member of the Criterium team is committed to
learning and understanding clients’ needs. By anticipating problems
before they affect our clients, we can ensure that all jobs are done
on time, correctly, and to a standard of excellence that exceeds client
expectations.
Below is a partial list of the client clinical services Criterium
provides:
- Annual reports and summaries
- Audit, lock, and transfer final database
- Biostatistics
- Budget management and tracking
- Central query generation and resolution
- Clinical program development
- CRF design and development
- Database design and development
- Double-key entry
- Drug accountability
- Electronic edit check development
- Enrollment tracking
- FaxForm design and development
- In-house computer-assisted data review
- Investigators meetings
- IRB qualification
- IVR script design and application development
- Medical coding
- Medical writing
- Multiple data input and export formats
- On-site monitor and regulatory training
- Protocol development
- QA audits
- QA conducted to FDA/ICH standards
- Site selection
- Site survey qualification
- Study closeout procedures
- Study initiation and monitoring
- Visit and CRF tracking
- Web-enabled forms design and development
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