Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Real-World Evidence Generation | Collect and analyze real-world data to support regulatory submissions and market access. | 12-24 weeks | $30,000 - $60,000 |
| Preclinical Research | Conduct studies on animals to evaluate the safety and efficacy of new treatments. | 12-24 weeks | $50,000 - $100,000 |
| Viral Vector Production | Produce viral vectors for gene therapy and vaccine development. | 12-24 weeks | $100,000 - $300,000 |
| Pricing and Reimbursement Analysis | Analyze pricing strategies and reimbursement pathways for drug products. | 4-6 weeks | $15,000 - $30,000 |
| Medical Writing | Create clinical study reports, regulatory documents, and scientific publications. | 4-8 weeks | $10,000 - $30,000 |
| Biostatistical Design | Use statistics to ensure appropriate pre-clinical and clinical study design. | 4-6 weeks | $10,000 - $15,000 |
| Adverse Event Reporting | Monitor and report adverse events related to drug products in clinical trials. | Ongoing | $10,000 - $20,000 annually |
| Life Cycle Assessment (LCA) | Analyze the lifecycles of products and services with regard to their environmental impacts. | 6-8 weeks | $15,000 - $25,000 |