As discussed in the Product Perspective, the Modernization of Cosmetics Regulation Act of 2022 (MoCRA) represents a major shift in cosmetic industry regulations. This article is one of a series of ...
DUBLIN--(BUSINESS WIRE)--The "How to Interview During GMP (Good Manufacturing Practice) Audits Training Course (Mar 12, 2026)" training has been added to ResearchAndMarkets.com's offering. Ensuring ...
Good Manufacturing Practice (GMP) is a system or protocol for ensuring product safety and consistency according to quality standards. GMP is important in all manufacturing industries, though it is ...
GUATEMALA CITY--(BUSINESS WIRE)--The tropical oil production and processing company, Agroaceite, was ranked with a 97.3% score by the Global STD certifier in Good Manufacturing Practices. The Good ...
Standard environmental monitoring with a cart of equipment that collects samples at pre-established locations of the cleanroom is a process that many have grown accustomed to performing. These ...
NOT FOR DISTRIBUTION TO NEWSWIRE SERVICES IN THE UNITED STATES OR FOR DISSEMINATION IN THE UNITED STATES. ANY FAILURE TO COMPLY WITH THIS RESTRICTION MAY CONSTITUTE A VIOLATION OF UNITED STATES ...
Successful Audit of the Company’s State-of-the-Art Manufacturing Facility Represents a Key Milestone Toward Plan to Commercialize D-PLEX₁₀₀ Globally PETACH TIKVA, Israel, Sept. 21, 2023 (GLOBE ...
Developing life-saving medicines is no easy feat. Manufacturing them quickly, consistently and with repeatability is even more challenging. The National Institute for Innovation in Manufacturing ...
DALLAS, July 15, 2024 (GLOBE NEWSWIRE) -- The Biotechnology and Healthcare Industry Alliance of North Texas (BHIANT) is proud to announce a strategic partnership between Dallas College and Panthera ...
The FDA final guidance for combination product good manufacturing practices (GMPs) grew by 10 pages compared to the draft guidance, but the final product was hailed as "a good guidance document" by ...
Manufacturers are usually subjected to a diverse variety of regulations typically established by international and regional bodies. Failure to comply can result in the loss of authorization and ...
With nearly 75% of the pharma units yet to begin upgradation work for their manufacturing facilities, the government might be forced to extend the deadline to implement revised Schedule M guidelines ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback