Regulatory Submission Timeline Planner (Excel Tracker)
Planning a multi-country study start-up means juggling wildly different regulatory and ethics review timelines. This Excel planner turns your planned submission date into best-case, typical and worst-case approval dates for up to 10 countries — and shows you which country is driving your critical path.
It's the downloadable, editable companion to our free Regulatory Timeline Calculator, built for teams who want to keep the model in their own files, share it internally, and adjust assumptions as new guidance comes in.
What's inside:
- Review-duration assumptions for 10 countries (US, EU, UK, Canada, Switzerland, Australia, Japan, South Korea, China, Brazil), covering both regulatory authority and ethics/IRB review
- Automatic handling of parallel vs. sequential review models per country
- A Submission Planner for up to 10 country entries, calculating best/typical/worst-case approval dates from your planned submission date
- A Dashboard identifying your global first-site-ready date and the country driving the critical path
Who it's for: Clinical operations and regulatory affairs teams planning multi-country study start-up timelines.
Please note: review-duration figures are illustrative planning estimates — always confirm current timelines with local regulatory counsel.
Format: One Excel workbook (.xlsx), fully editable, in English. Instant download after purchase.