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 |
| 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 |
| Medical Writing | Create clinical study reports, regulatory documents, and scientific publications. | 4-8 weeks | $10,000 - $30,000 |
| Data Visualization | Visualize data collected from clinical trials and/or clinical research. | 3-5 weeks | $3,000 - $7,000 |
| Orphan Drug Designation | Prepare and submit applications for orphan drug designation to regulatory agencies. | 8-12 weeks | $20,000 - $40,000 |
| Patient-Reported Outcomes | Develop and validate patient-reported outcome measures for use in clinical trials. | 8-12 weeks | $20,000 - $40,000 |
| Abstracts | Request services related to the writing and review of abstracts. | 2-4 weeks | $3,000 - $5,000 |
| Viral Vector Production | Produce viral vectors for gene therapy and vaccine development. | 12-24 weeks | $100,000 - $300,000 |
| Companion Diagnostics Development | Develop diagnostic tests that are paired with specific therapeutic products. | 16-24 weeks | $50,000 - $150,000 |
| Stability Studies | Evaluate the stability of drug products over time. | 12-24 months | $50,000 - $100,000 |