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Post-market safety studies


First major overhaul of medical device regulation comes into force across Great Britain
MHRA published 16 June 2025 New Post-Market Surveillance (PMS) regulations have taken effect across Great Britain, requiring medical...
kenashman
Jun 171 min read
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Real-World pharmacovigilance analysis of drug-related conjunctivitis using the FDA adverse event reporting system database
Nature 18 April 2025 Drug-related conjunctivitis can compromise ocular health and quality of life. To evaluate its epidemiology, this...
kenashman
May 131 min read
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Real-World Evidence (RWE) in Drug Safety Market Projected To Witness Massive Growth, 2025-2032
Coherent Market Insights 26 March 2025 The global Real-World Evidence (RWE) in Drug Safety market is estimated to be valued at USD 8.03...
kenashman
May 81 min read
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A Real-World Pharmacovigilance Study of FDA Adverse Event Reporting System Events for Avelumab
Cureus : Published 27 March 2025 This study utilized data from the FDA Adverse Event Reporting System (FAERS) to investigate adverse drug...
kenashman
May 81 min read
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Post-market safety profile of cefiderocol: a real-world pharmacovigilance exploratory analysis based on U.S. FDA adverse event reporting system (FAERS)
BMC Pharmacology and Toxicology 26 (1) March 2025 Cefiderocol is a new drug class, which is approved to treat Gram-negative bacteria...
kenashman
May 81 min read
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