Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Orphan Drug Designation | Prepare and submit applications for orphan drug designation to regulatory agencies. | 8-12 weeks | $20,000 - $40,000 |
| Regulatory Submissions | Prepare and submit documentation to regulatory agencies for product approval. | 8-12 weeks | $40,000 - $80,000 |
| Formulation Development | Develop the composition of drug products to ensure efficacy and stability. | 8-12 weeks | $30,000 - $60,000 |
| 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 |
| Medical Affairs Support | Provide support for medical affairs activities, including medical communications and KOL engagement. | Ongoing | $20,000 - $40,000 annually |
| Clinical Protocol Design & Development | Creation of a clinical protocol document detailing how a clinical trial is designed. | 6-8 weeks | $15,000 - $25,000 |
| HTA Evidence Preparation/ Dossier Development | Perform evidence preparation and collection needed for a Health Technology Assessment (HTA). | 8-10 weeks | $25,000 - $50,000 |
| 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 |
| Market Access Strategy | Develop strategies to ensure products gain market access and reimbursement. | 6-8 weeks | $25,000 - $50,000 |