Medical device equipment manufacturers work in an environment where product quality isn't just a competitive advantage, it's a regulatory necessity with direct implications for patient safety. As ...
In pharmaceutical manufacturing, cleaning validation is an essential stage of verifying that the manufacturing process is suitable. As an integral stage of the cleaning validation program, analytical ...
Dublin, April 15, 2026 (GLOBE NEWSWIRE)-- The "Cleaning Validation - Best Practice in Pharmaceuticals (June 23rd - June 24th, 2026)" training has been added to ResearchAndMarkets.com's offering. Learn ...
A lifecycle approach can be used to develop GMP-compliant cleaning procedures for continuous manufacturing of solid-dosage pharmaceuticals. It is now possible, as demonstrated by Janssen (1), for drug ...
With COVID-19 vaccine facilities receiving recent citations, it is evident that failure to meet cleaning and sanitization requirements puts patients, facilities, and operators at risk. Keeping ...
The pharmaceutical industry is undergoing a transformative era driven by increasingly stringent global regulatory requirements, significantly impacting operational processes, particularly those ...
ISO 19227 Implants for Surgery--Cleanliness of Orthopedic Implants--General Requirements is a long-awaited guidance document that was finalized and published early 2018. This guidance document is ...
ValGenesis, Inc., the global leader in enterprise digital validation, successfully concluded two ValConnect Innovation Day events in Lisbon, Portugal, and Research Triangle Park (RTP), North Carolina, ...
The majority of food manufacturers would accept that cleaning is a vital function within food processing, especially with respect to issues of hygiene. However, cleaning is also a defining process in ...
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