Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Pharmacovigilance Services | Monitor and report adverse effects related to drug use. | Ongoing | $20,000 - $40,000 annually |
| Real-World Evidence Generation | Collect and analyze real-world data to support regulatory submissions and market access. | 12-24 weeks | $30,000 - $60,000 |
| HTA Evidence Preparation/ Dossier Development | Perform evidence preparation and collection needed for a Health Technology Assessment (HTA). | 8-10 weeks | $25,000 - $50,000 |
| Patient Recruitment | Develop strategies to recruit and retain participants for clinical trials. | 8-12 weeks | $20,000 - $40,000 |
| Regulatory Document Submission | Prepare and submit regulatory documents to agencies like the FDA and EMA. | 6-8 weeks | $15,000 - $30,000 |
| Consensus Reports | Develop and submit a report that examines a scientific or medical issue. | 4-6 weeks | $5,000 - $10,000 |