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Pharmaceutical Ingredient Software

6 software items found

DDDPlus - In Vitro Dissolution Simulation Software

DDDPlus - In Vitro Dissolution Simulation Software

by:Simulations Plus   based inLancaster, CALIFORNIA (USA)
The DDDPlus software from Simulations Plus is a renowned tool for conducting in vitro dissolution experiments specifically tailored for pharmaceutical dosage forms. Designed for formulation and analytical scientists, it facilitates the modeling and simulation of the dissolution process involving active pharmaceutical ingredients (API) and ...
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Aicos - Version Schedule++ - Scheduling Software for Chemical and Pharmaceutical Industries

Aicos - Version Schedule++ - Scheduling Software for Chemical and Pharmaceutical Industries

by:AICOS Technologies AG   based inAllschwil, SWITZERLAND
This powerful detailed scheduling software was developed specifically for the needs of the process industries (chemicals, pharmaceuticals, cosmetics, food, etc.). It offers the planner a detailed visualization of the schedule as well as the possibility to keep at each moment an overview over all resources needed for production (devices, manpower, raw materials,...). Different scheduling ...
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Nova Stability - Stability Management System Software

Nova Stability - Stability Management System Software

by:Novatek International   based inMontreal, QUEBEC (CANADA)
Determining of the shelf-life of a pharmaceutical product is critical for understanding how long that product can maintain original quality specifications. Product used after the expiration date can negatively impact a patient. For this reason the shelf-life determination must be accurate. The stability studies required to evaluate shelf-life can take several years to complete. Mistakes made ...
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OOS Software - Out of Specification Software

OOS Software - Out of Specification Software

by:MasterControl, Inc   based inSalt Lake City, UTAH (USA)
OOS Software to Automate Out of Specification (OOS) Processes to Comply with FDA CGMPs and 21 CFR Part 211 and Part 820 Regulations. In the FDA environment, specifications are essential in maintaining quality. CGMP regulations for finished pharmaceuticals (21 CFR Parts 210-211) and medical devices (21 CFR Part 820) require strict conformance to approved specifications which can be acheived easily ...
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Sphere Fluidics - Version ESI-Mine - Platform for High-Throughput, Miniaturised Electrospray Injection Mass Spectrometry (ESI-MS)

Sphere Fluidics - Version ESI-Mine - Platform for High-Throughput, Miniaturised Electrospray Injection Mass Spectrometry (ESI-MS)

Manufactured by:Sphere Fluidics Limited   based inCambridge, UNITED ARAB EMIRATES
ESI-Mine™ can test up to 200,000 biomolecular samples (e.g. peptides, enzymes, antibodies, metabolites and small molecules) per day in miniaturized volumes of 500-700pL (picodroplets) facilitating more efficient screening and analysis in bioproduction or synthetic biology processes. Applying this novel approach, researchers can create a large library of picodroplets containing ...
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EVK SQALAR - Qualitative and quantitative Analysis Software Tools

EVK SQALAR - Qualitative and quantitative Analysis Software Tools

Manufactured by:EVK DI Kerschhaggl GmbH   based inRaaba/Graz, AUSTRIA
EVK SQALAR is a multifunctional quantitative analysis software tool for multivariate measurements of chemical properties. It is a software tool suitable for sorting, inspection and monitoring applications, both in-line and at-line, and also in ...
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