AML Clinical Services offers a wide range of services for the conduct of clinical research. Our tailored service matches your needs:
- Clinical training for CTAs / CRAs (in-house training, and on the job training)
- Clinical training for study site personnel
- Feasibility studies
- Research Site selection and pre-study assessments
- Site initiation
- Organisation of investigator's meetings
- Submission to ethics committees
- Submission to Competent Authorities
- Project tracking /status reporting
- Budget negotiation
- Auditing assistance
- Writing- /translation of study related documents
- CRF-design
- Trial & Site management
- Monitoring of clinical trials (Phase I to Phase IV, PMOS, IIS)
- Secondary monitoring
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