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ExoPTEN is being developed as a first-in-class, exosome-based therapy targeting high-impact neurological indications, including acute spinal cord injury, optic nerve damage, facial nerve injury, and ...
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AllAfrica on MSNNigeria: NAFDAC Seals 39 Illegal Water Factories in Five MonthsMr Benu explained that a total of 43 packaged water facilities were inspected during the periodThe National Agency for Food and Drug Administration and Control (NAFDAC) Ogun II Office, Ota, has sealed ...
Bigshot and Delta McKenzie offer variety of archery targets including augmented reality 3D animal targets for hunter ...
Eye care products, including artificial tears and drops, are being recalled by their distributor. The recall responds to deviations from good manufacturing practices discovered during a U.S. Food ...
An artificial tear solution is one of five ophthalmic products now under recall ... deviations from the agency’s current good manufacturing practice regulations and a “lack of assurance ...
BRS Analytical Service has issued a voluntary recall of multiple ophthalmic products due to FDA-identified ... Administration identified current Good Manufacturing Practice (cGMP) deviations ...
Eye drop recall: Nearly 76,000 cases of eye care products are feared to be of ‘unacceptable quality’
If you’re a frequent eye drop user, now’s the time to check your medicine cabinet: The pharmaceutical lab BRS Analytical Service, LLC has issued a voluntary recall of five different ophthalmic ...
The recall is due to current Good Manufacturing Practice (cGMP) deviations, which may lead to products of unacceptable quality, posing potential risks to users. The affected products include ...
has completed its first Good Manufacturing Practice ("GMP") Clinical Batch of its pharmaceutical-grade oral mucosal formulation of aspirin that utilizes Aspire's fast-acting formulation.
However, the compliance deadline for Good Manufacturing Practices (GMP) under Schedule M of the Drugs and Cosmetics Act was extended from January 1, 2025, to December 31, 2025, emphasising the ...
Developed and overseen by the International Organization for Standardization, ISO 22716 is the standard for Cosmetics – Good Manufacturing Practices (GMP). The standard offers guidance on ...
Adherence to the CGMP regulations assures the identity, strength, quality, and purity of drug products by requiring that manufacturers of medications adequately control manufacturing ... 211 details ...
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