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02
Clinical study and trial design
Advice on the design of observational studies and clinical trials: questions, populations, endpoints, comparators and analysis plans that will withstand review.
Typical questions
- Which primary endpoint answers the question and is feasible in this population?
- How large, how long, and with what comparator?
- Which design, parallel, adaptive, platform, pragmatic or registry-based, fits the evidence gap and the budget?
- How should the protocol anticipate ethics-committee and regulatory questions?
What you receive
- 1Design review memo with alternatives and trade-offs
- 2Input on protocol structure and the statistical analysis plan outline
- 3Preparation for scientific advisory or investigator meetings
Well suited to
Academic investigators, clinical research units, sponsors and CROs seeking senior scientific input.
Veritas does not act as sponsor, CRO or regulatory representative; we advise the teams who do.