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To help you protect, manage and enforce your intellectual property (IP) rights in Philippines.
Explainer for the pharmaceutical industry on the implementation of Pharmacovigilance requirements during the transition time from the date the revised VMR have effect in GB to 17 May 2027.
The aim of this paper is to present a decolonial model of supervision called “WONDERFUL Supervision”.
Information for manufacturers of software as a medical device, detailing events that may cause indirect harm and are therefore reportable.
VMD response to concerns raised following media reports of serious adverse events in dogs administered Librela.
Guidelines for the monitoring of volume individual voluntary arrangement (IVA) and protected trust deed (PTD) providers
Armilla Verified is Armilla’s third-party verification of AI-powered products. It empowers AI vendors and enterprises alike to assure the quality and reliability of their AI solutions.
To assist sponsors and those conducting trials on implementing adequate oversight and monitoring processes for trials of investigational medical products.
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