Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Site Selection and Feasibility | Identify and evaluate potential sites for clinical trials. | 6-8 weeks | $10,000 - $20,000 |
| Health Technology Assessment Submission (HTA Submission) | Analyze and submit the considerations of a drug, device, or clinical procedure to regulatory agencies. | 10-14 weeks | $35,000 - $70,000 |
| Pharmacovigilance Services | Monitor and report adverse effects related to drug use. | Ongoing | $20,000 - $40,000 annually |
| Patient Recruitment | Develop strategies to recruit and retain participants for clinical trials. | 8-12 weeks | $20,000 - $40,000 |
| Pharmaceutical Manufacturing | Manufacture drug products under GMP conditions. | 8-16 weeks | $100,000 - $500,000 |
| Clinical Protocol Design & Development | Creation of a clinical protocol document detailing how a clinical trial is designed. | 6-8 weeks | $15,000 - $25,000 |
| HTA Evidence Preparation/ Dossier Development | Perform evidence preparation and collection needed for a Health Technology Assessment (HTA). | 8-10 weeks | $25,000 - $50,000 |
| Orphan Drug Designation | Prepare and submit applications for orphan drug designation to regulatory agencies. | 8-12 weeks | $20,000 - $40,000 |
| Companion Diagnostics Development | Develop diagnostic tests that are paired with specific therapeutic products. | 16-24 weeks | $50,000 - $150,000 |