Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Data Visualization | Visualize data collected from clinical trials and/or clinical research. | 3-5 weeks | $3,000 - $7,000 |
| Clinical Trial Design | Develop study-related protocols, case report forms (CRFs), and database tools. | 8-12 weeks | $20,000 - $40,000 |
| Medical Affairs Support | Provide support for medical affairs activities, including medical communications and KOL engagement. | Ongoing | $20,000 - $40,000 annually |
| GMP Audits | Conduct audits of manufacturing facilities to ensure compliance with GMP standards. | 2-4 weeks | $10,000 - $20,000 |
| Biostatistical Design | Use statistics to ensure appropriate pre-clinical and clinical study design. | 4-6 weeks | $10,000 - $15,000 |
| Health Technology Assessment Submission (HTA Submission) | Analyze and submit the considerations of a drug, device, or clinical procedure to regulatory agencies. | 10-14 weeks | $35,000 - $70,000 |
| Orphan Drug Designation | Prepare and submit applications for orphan drug designation to regulatory agencies. | 8-12 weeks | $20,000 - $40,000 |
| HTA Evidence Preparation/ Dossier Development | Perform evidence preparation and collection needed for a Health Technology Assessment (HTA). | 8-10 weeks | $25,000 - $50,000 |
| Analytical Testing | Conduct laboratory tests to ensure the quality and safety of drug products. | 4-8 weeks | $15,000 - $30,000 |