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Microbial burden assessment of solid pharmaceutical products

European Pharmaceutical Review

The paper reported that benefits of these alternative methodologies include “the ability to respond more quickly to adverse microbiological results, as well as leading to fewer waste products”. The post Microbial burden assessment of solid pharmaceutical products appeared first on European Pharmaceutical Review.

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Leading innovators in ssRNA virus peptides for the pharmaceutical industry

Pharmaceutical Technology

J&J develops, manufactures, and sells pharmaceutical products, medical devices, and consumer products.

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The key role of GMP analytical testing for drug products

European Pharmaceutical Review

Analytical testing is an essential part of guaranteeing the quality, safety and effectiveness of pharmaceutical products. During the manufacturing processes, pharmaceutical products must be made correctly every time, due to the high level of regulatory oversight.

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Leading pharmaceutical wholesalers

Pharmaceutical Technology

Wholesale pharmaceutical companies also offer services such as end formulation contracts, which help pharmaceutical marketing companies and pharmacies locate manufacturing units across regions and coordinate negotiations when required. Discover the top pharmaceutical wholesalers. GDP and GMP advisory.

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Leading freeze-drying systems suppliers for the pharmaceutical industry

Pharmaceutical Technology

Freeze drying is a crucial technique to prolong the shelf life of pharmaceutical products. Also known as lyophilisation, the technique stabilises and preserves sensitive products such as biologics, and diagnostic kits, in a permanently storable state.

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Regulatory Compliance: Ensuring that pharmaceutical products meet all regulatory requirements and guidelines, including safety, efficacy, labelling, and post-marketing surveillance

eMediWrite

From the examination of raw materials through the release of the finished packaged product, Quality Control Authorities like Central Drugs Standard Control Organisation in India established under the Drugs & Cosmetics Act, 1940. They play a crucial role in assuring the efficacy and safety of products given to patients.

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INTERPHEX 2023 – experience science through commercialisation

European Pharmaceutical Review

INTERPHEX is set to bring leading brands and professionals together once again with new features, a reimagined Show Floor and returning Show Floor favourites. From development to distribution, INTERPHEX is the leading global event that takes you through all stages of the pharmaceutical product development lifecycle.