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5 d

What Global Manufacturers Must Know About NMPA Policies?
This blog starts with key NMPA policies global manufacturers must know, covering compliance, regulatory updates, and pathways for China market access.
https://www.freyrsolutions.com..../blog/what-global-ma

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5 d

SAHPRA Drug Registration Process - Freyr Solution
This blog talks about the SAHPRA drug registration process in South Africa—offering pharmaceutical companies a clear, step-by-step guide to get approvals efficiently.
https://www.freyrsolutions.com..../blog/sahpra-drug-re

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5 d

Pharmacovigilance Hong Kong: Component of Product Lifecycle Management
This blog talks about pharmacovigilance in Hong Kong, highlighting its role in drug safety, regulatory compliance, and effective product lifecycle management.
https://www.freyrsolutions.com..../blog/pharmacovigila

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5 d

Foreign GMP Inspection Malaysia: Overseas Pharma Sites Must Comply
This blog starts with Malaysia’s Foreign GMP inspection, explaining why overseas pharma sites must comply and how to prepare for regulatory approval.
https://www.freyrsolutions.com..../blog/foreign-gmp-in

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5 d

10 FAQ's About Drug Registration in China
This blog starts with answers to 10 frequently asked questions about drug registration in China, tailored for manufacturers navigating regulatory requirements and compliance.
https://www.freyrsolutions.com..../blog/10-frequently-

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UK MHRA mandates Medical Device manufacturers located outside the United Kingdom (UK) and without any local business offices for MHRA UK Responsible Person registration. Manufactureres need to appoint a United Kingdom Responsible Person (UKRP) or UK Representative on their behalf, as a pre-requisite for device registration and launch of the device in the United Kingdom.

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