2013 Documentation Pharmaceutical Manufacturing 
European Pharmaceutical Review
JULY 5, 2023
43: Identification and Classification of Nonconformities in Moulded and Tubular Glass Containers for Pharmaceutical Manufacturing. Having been originally published in 2007, then revised in 2013, this latest 2023 edition addresses evolving standards and container types.
Express Pharma
MARCH 16, 2025
What are the top 3 trends that defined pharma manufacturing in India and globally in 2024? In 2024, the pharmaceutical manufacturing landscape underwent transformative changes, driven by technological innovations, regulatory adaptations, and evolving global demands. per cent of global patents to almost 2 per cent.
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European Pharmaceutical Review
APRIL 8, 2025
Implementing PAT in (bio)pharmaceutical manufacturing New sensors or larger equipment with more complex setups (software and hardware) require stringent procedures to become fully implemented in a good manufacturing practice (GMP) manufacturing facility.
pharmaphorum
OCTOBER 7, 2020
When I finally sought treatment in 2013, I learned how to turn my ADHD into a strength by better managing it. Done is here to combat these stereotypes, and is working to remove barriers to treatment such as requirements and expectations about frequency of visits, documentation, medication choice and choice of provider.
Ramblings of a pharmacist
SEPTEMBER 26, 2023
First of all - the text of the law passed by Congress and signed into law on 11/27/2013 is available here, on page 562-595. As I’ve discussed before on this blog, counterfeit products DO exist and even have the apparently appropriate T3 documents to validate their legitimacy. .”
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