Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Site Selection and Feasibility | Identify and evaluate potential sites for clinical trials. | 6-8 weeks | $10,000 - $20,000 |
| Custom Synthesis | Synthesize custom compounds for research and development purposes. | 8-12 weeks | $20,000 - $50,000 |
| Regulatory Strategy Consulting | Provide advice on regulatory strategy for product development and approval. | 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 |
| Clinical Trial Monitoring | Oversee the conduct of clinical trials to ensure compliance with protocols. | Ongoing | $10,000 - $20,000 per site |
| Medical Writing | Create clinical study reports, regulatory documents, and scientific publications. | 4-8 weeks | $10,000 - $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 |
| Cell Line Development | Develop and characterize cell lines for use in biopharmaceutical production. | 12-16 weeks | $50,000 - $100,000 |
| Clinical or Speaker Training Webinar Slide Decks | Develop and design slide decks for clinical or speaker training webinars. | 2-3 weeks | $2,000 - $4,000 |
| Data Visualization | Visualize data collected from clinical trials and/or clinical research. | 3-5 weeks | $3,000 - $7,000 |