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Polymorphism, Salts & Crystallization Brochure

Polymorphism, Salts & Crystallization Brochure

Polymorphism, Salts & CrystallizationAn Integrated Approach to Solid-State Development Amazing where you can go-1-Introduction: Solid-State DevelopmentThe majority of drugs are administered as solids. This means that apart from the molecular structure of the active ingredient, solid-state properties significantly influence the performance of the final product.Often new ...
BySolvias AG

WasteLog - Tools and Solutions for Drug Diversion Prevention - Brochure

WasteLog - Tools and Solutions for Drug Diversion Prevention - Brochure

WasteLog® can verify the identity and concentration of liquid pharmaceuticals in an instant. Preventing drug diversion of controlled substances used in the OR requires a quick and reliable method of monitoring and controlling your returns. With its flexibility, efficient workflow and ease of use, WasteLog® can become an essential part of your Drug Diversion ...
ByCodonics

LeKrius 3D Storage Bag - Brochure

LeKrius 3D Storage Bag - Brochure

The multi-layer co-extrusion film used for the 3D storage bags ensures extremely low gas transmission, good physical strength, excellent chemical compatibility and biocompatibility of the aseptic storage bags. The bags can be safely used for storage and transport of various biopharmaceutical liquids. The standard 3D storage bags are available in various types and specifications from 50 L to 3000 ...
ByLePure Biotech

Bio Reme - Bioculture for Pharma - Brochure

Bio Reme - Bioculture for Pharma - Brochure

Bio Reme Pharma is very much effective for partial degradation and sustaining of biodegradable solvents, microbicides, antimicrobial substances and drugs intermediated in low concentrations. Bio Reme Pharma is capable to withstand high shock load which is happens due to change in production and R & D of new products in pharmaceutical, Nutraceuticals, Formulations, Antibiotics & Drugs, and ...
ByGreencraft Labs Pvt. Ltd

Extractables and Leachables Testing In Pharma - White Paper

Extractables and Leachables Testing In Pharma - White Paper

Containers meant to protect a drug from environmental contamination are actually themselves a source of contamination. at what stage in the development of a drug e/l becomes an issue, depends on the development program. certainly, when the final container closure system and/or de-vice is to be selected, e/l programs become mandatory. ...
BySolvias AG
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