AdHoc's experienced physicians and clinical research professionals assist you in the planning, of clinical trials.
We can help you in building the best protocols by advising on study endpoints, eligibility criteria, study assessment and design options, and writing protocol synopses.
Protocols are designed to address timely recruitment of patients, and a provision of sound answers to scientific questions. You will receive excellent clinical study oversight which is paramount for a successful, timely, and cost-efficient drug development process.
Ah Hoc clinical team can support you with the following services:
- Study Design
- Eligibility criteria analysis
- Endpoints definitions
- Protocol development
- Assessment of study competitive environment
- Clinical centres selection
- Investigator qualification
- Assessment of patient recruitment strategy