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Sunday, 02/18/2024 10:18:04 PM

Sunday, February 18, 2024 10:18:04 PM

Post# of 711653
Could it be that submitting in the UK will lead to approval in all these Orbis partner countries! Fingers crossed!

Project Orbis is coordinated by the US Food and Drug Administration (FDA). Alongside MHRA, it involves the regulatory authorities of:

Australia (Therapeutic Goods Administration (TGA))

Canada (Health Canada)

Singapore (Health Sciences Authority (HSA))

Switzerland (Swissmedic)

Brazil (Agência Nacional de Vigilância Sanitária (ANVISA))

Israel (Ministry of Health)

Project Orbis Partners (POPs) may propose products for inclusion in the scheme. Each country remains fully independent on their final regulatory decision.

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