Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Health & Pharmacoeconomics | Identify, measure, and compare the cost-benefit ratio of products and services. | 6-8 weeks | $20,000 - $35,000 |
| Regulatory Strategy Consulting | Provide advice on regulatory strategy for product development and approval. | 4-8 weeks | $15,000 - $30,000 |
| Pharmaceutical Manufacturing | Manufacture drug products under GMP conditions. | 8-16 weeks | $100,000 - $500,000 |
| Clinical Trial Design | Develop study-related protocols, case report forms (CRFs), and database tools. | 8-12 weeks | $20,000 - $40,000 |
| Real-World Evidence Generation | Collect and analyze real-world data to support regulatory submissions and market access. | 12-24 weeks | $30,000 - $60,000 |
| Orphan Drug Designation | Prepare and submit applications for orphan drug designation to regulatory agencies. | 8-12 weeks | $20,000 - $40,000 |
| Preclinical Research | Conduct studies on animals to evaluate the safety and efficacy of new treatments. | 12-24 weeks | $50,000 - $100,000 |
| Cell Line Development | Develop and characterize cell lines for use in biopharmaceutical production. | 12-16 weeks | $50,000 - $100,000 |
| Custom Synthesis | Synthesize custom compounds for research and development purposes. | 8-12 weeks | $20,000 - $50,000 |
| Companion Diagnostics Development | Develop diagnostic tests that are paired with specific therapeutic products. | 16-24 weeks | $50,000 - $150,000 |