Molecule2Market
Feasibility and site selection, clinical development services and study start-up.
What they do
From their website
Services
- Project feasibility (opens in a new tab)
- Project management (opens in a new tab)
- Local safety reporting (opens in a new tab)
- Site close out (opens in a new tab)
- Australian sponsorship (opens in a new tab)
- Resident director (opens in a new tab)
- Study protocols (opens in a new tab)
- Investigator's brochures (opens in a new tab)
- Abbreviated clinical study reports (opens in a new tab)
- Interim safety reports (opens in a new tab)
- Patient information sheets (opens in a new tab)
- SOP development (opens in a new tab)
- Investigator site audits (opens in a new tab)
- CRO audits (opens in a new tab)
- Pharmacovigilance audits (opens in a new tab)
- GLP audits (opens in a new tab)
- Systems audits (opens in a new tab)
- Trial master file audits (opens in a new tab)
- EC/IRB audits (opens in a new tab)
- Mock regulatory agency audits (opens in a new tab)
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Services
- Protocol development/review (opens in a new tab)
- Analysis plan support (opens in a new tab)
- Technical document preparation (opens in a new tab)
- Study-specific training (opens in a new tab)
- Data safety monitoring (opens in a new tab)
- Biostatistical support (opens in a new tab)
- R&D tax expert (opens in a new tab)
- ECRF/CRF design (opens in a new tab)
- EDC user acceptance testing (opens in a new tab)
- DSMB meetings (opens in a new tab)
- SAE review (opens in a new tab)
- Pharmaceutical R&D (opens in a new tab)
- Regulatory registration (opens in a new tab)