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South Africa: Renewal of Medicines Certificate of Registration Framework
On 26th August, 2025 the South African Health Products Regulatory Authority (SAHPRA)Â has introduced a structured framework for the...

Sharan Murugan
Aug 282 min read
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Navigating UK MHRA Guidance: Registration and Regulation of Medical Devices in the UK
The Medicines and Healthcare Products Regulatory Agency (MHRA) Â oversees the regulation and registration of medical devices within the...

Sharan Murugan
Feb 182 min read
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USFDA Guidance: REMS Logic Model: A Framework to Link Program Design With Assessment
The U.S. Food and Drug Administration (FDA) Center for Drug Evaluation and Research and Center for Biologics Evaluation and Research...

Sharan Murugan
May 11, 20242 min read
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