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If regulatory submissions proceed as expected, the earliest plausible timeline for a market authorisation decision in the UK or Europe would be 2026 or 2027 — though this is subject to the pace of regulatory review, the completeness of the submission package, and any additional data requests from the MHRA or EMA

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Prompted by these authoritative positions and in compliance to a precautionary principle, the Health Authorities of France, UK, Italy, and many other countries adopted the warning on NSAIDs recommendation

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