Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Analytical Testing | Conduct laboratory tests to ensure the quality and safety of drug products. | 4-8 weeks | $15,000 - $30,000 |
| Scientific Advisory Board Management | Organize and manage meetings with scientific advisory boards to guide research and development. | Ongoing | $15,000 - $30,000 annually |
| Patient-Reported Outcomes | Develop and validate patient-reported outcome measures for use in clinical trials. | 8-12 weeks | $20,000 - $40,000 |
| Clinical Protocol Design & Development | Creation of a clinical protocol document detailing how a clinical trial is designed. | 6-8 weeks | $15,000 - $25,000 |
| Pharmacovigilance Services | Monitor and report adverse effects related to drug use. | Ongoing | $20,000 - $40,000 annually |
| Emerging Market Opportunities | Analyze risks and opportunities in new markets for patient access to new treatments. | 6-8 weeks | $15,000 - $30,000 |
| Real-World Evidence Generation | Collect and analyze real-world data to support regulatory submissions and market access. | 12-24 weeks | $30,000 - $60,000 |
| Medical Writing | Create clinical study reports, regulatory documents, and scientific publications. | 4-8 weeks | $10,000 - $30,000 |
| Process Development | Optimize the manufacturing process for drug products. | 12-16 weeks | $50,000 - $100,000 |
| Health Technology Assessment | Conduct a multidisciplinary process to determine the value of a health technology. | 8-12 weeks | $30,000 - $60,000 |