Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Adverse Event Reporting | Monitor and report adverse events related to drug products in clinical trials. | Ongoing | $10,000 - $20,000 annually |
| Patient Recruitment | Develop strategies to recruit and retain participants for clinical trials. | 8-12 weeks | $20,000 - $40,000 |
| HTA Evidence Preparation/ Dossier Development | Perform evidence preparation and collection needed for a Health Technology Assessment (HTA). | 8-10 weeks | $25,000 - $50,000 |
| Regulatory Submissions | Prepare and submit documentation to regulatory agencies for product approval. | 8-12 weeks | $40,000 - $80,000 |
| Companion Diagnostics Development | Develop diagnostic tests that are paired with specific therapeutic products. | 16-24 weeks | $50,000 - $150,000 |
| Consensus Reports | Develop and submit a report that examines a scientific or medical issue. | 4-6 weeks | $5,000 - $10,000 |
| Regulatory Strategy Consulting | Provide advice on regulatory strategy for product development and approval. | 4-8 weeks | $15,000 - $30,000 |