Drug Delivery Products & Reviews

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Drug Delivery refers to dosage form, route of administration, formulations, technologies, and systems for transporting a pharmaceutical compound in the body as needed to safely achieve its desired therapeutic effect. Drug delivery is often approached via the biopharmaceutical or small molecule drug's formulation, but it may also involve medical devices or drug-device combination products. Considerations include instrumentation, software and services.

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Agilent 280-DS Mechanical Qualification System

Agilent Technologies

The Agilent 280-DS mechanical qualification system (MQS) enables the physical qualification of any dissolution apparatus per enhanced Mechanical Qualification (eMQ) guidelines. Once positioned, the innovative sensing technology allows hands-free measurements to be performed in seconds while measuring and recording critical physical parameters.

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709-DS Dissolution Apparatus

Agilent Technologies

Using the same platform as the 708-DS, the 709-DS Dissolution Apparatus ensures productivity, reproducibility and ease of use combined with the convenience of a bath-free design. The 709-DS reduces media heating time with Direct Vessel Heating (DVH) capabilities while insulating the vessel from environmental factors and eliminating water bath cleaning. The exclusive design of the chemically resistant, DVH TruAlign vessel incor…

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Parteck® SLC Excipients

Merck

Created specifically for solid dosage forms, Parteck® excipients are distinguished by outstanding functionalities and a unique particle structure. All Parteck® products are developed under our Functional Particle Engineering concept comprising advanced EMD Millipore technologies for quite extraordinary functionally relevant particle properties. These properties of Parteck® excipients offer decisive advantages to the formulato…

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EMPROVE® api Portfolio

Merck

Registering an API is complex and thus very time-consuming. That’s why we’ve offer EMPROVE® api: high-quality raw materials for use as active pharmaceutical ingredients. EMPROVE® api raw materials are produced according to cGMP guideline ICH Q7. What’s more, all of our EMPROVE® API production plants are located in Western Europe and follow current environmental standards. And in order to support your products’ compliance with…

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EMPROVE® bio Portfolio

Merck

Raw material qualification is a key factor in assuring the quality and safety of biopharmaceuticals. Even still, performing tests and compiling required documentation on your own is costly and time-consuming. Enter EMPROVE® bio raw materials – your solution for getting products to market faster. EMPROVE® bio raw materials for use in biopharmaceutical production offer specifications adapted for use in upstream or downstream pr…

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EMPROVE® exp Portfolio

Merck

EMPROVE® exp for use as excipient As drug approval procedures grow stricter, regulatory requirements are becoming more demanding for excipients. Our high-quality EMPROVE® exp raw materials for use as excipients not only comply with relevant regulations, but also come with detailed documentation, facilitating lower costs of qualification, so you can get to market faster. EMPROVE® exp dossiers comprise information on the manuf…

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