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Drug Formulation Services
36 services found
Manufactured by:CD Formulation based in, NEW YORK (USA)
In order to ensure the safety of drug product quality, the packaging system that comes into direct contact with the drug product needs to meet compatibility requirements. Compatibility studies refer to the process of evaluating packaging components or systems that are in direct contact with the drug product without serious, or unacceptable, ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
One-Stop Solution for Small Molecule Drug Formulation: Small molecule drugs are chemically synthesized small molecules of active substances. Small molecule components can be made into tablets or capsules that are easily absorbed by the body. CD Formulation has extensive research experience in drug ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
The residue on ignition check method is used as an indicator to control the quality of API. CD Formulation offers a professional drug residue on ignition test, which assesses the quality of a drug by heating the drug to char and then ashing it. CD Formulation's business covers all aspects of drug ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
CD Formulation's Contract Development and Manufacturing (CDMO) division is a leader in drug development and drug delivery pathway development, offering services such as bioresorbable particle system development. CD Formulation also offers integrated services from evaluation of drug formulation to ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Swelling Performance Evaluation for Microspheres & Microneedles: Swelling test is one of the basic testing methods for microneedles and microspheres material properties. The purpose is to test the ability of microneedles and microspheres materials to absorb or release drugs as substrates for sustained drug release systems. The swelling tests of microspheres and ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Lyophilized formulation is designed around their API and in most cases include many excipients, such as buffers, fillers, tension regulators and stabilizers. CD Formulation can screen out suitable excipient formulation for customers, so that freeze-dried products with long shelf life and stable biological activity level can be prepared. Learn more at ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
The characterization and analysis of the phases in APIs and formulations is important to ensure that the drug properties are maintained at all times. Failure to fully understand the interactions of the phases may cause changes in solubility and/or dissolution, which can directly affect drug absorption. CD Formulation has mastered ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
The characterization and analysis of the phases in APIs and formulations is important to ensure that the drug properties are maintained at all times. Failure to fully understand the interactions of the phases may cause changes in solubility and/or dissolution, which can directly affect drug absorption. CD Formulation has mastered ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Preparation of Nano-vesicles for Encapsulating Protein Drugs: CD Formulation can customize the vesicles that encapsulate protein drug molecules to avoid the technical problems of drug rupture and leakage during in vivo delivery. Our technical team will perform a full range of analytical tests to ensure that the product meets your ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Poor solubility and low bioavailability of drugs are an important link that affects drug development. CD Formulation provides a variety of ways to improve these shortcomings of drugs, including physical and chemical methods. Among them, physical modification methods include eutectic method in addition to nano-grinding and ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Sterile powder for injection made by freeze-drying method is called lyophilized formulation, which is one of the important alternatives to liquid formulations. Any drug that is unstable at room temperature (e.g. interferon, coenzyme A and blood products) needs to be made into lyophilized formulation. Since biopharmaceutical ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Exenatide Microneedle Patch Preparation: The use of hydrophobic mold material to prepare microneedles maintains the integrity of the needle shape and the uniformity of drug loading. CD Formulation provides a microinjection method for the minimally invasive transdermal administration of exenatide to address the short half-life of exenatide, the defects of ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Melatonin Microneedle Patch Preparation: In order to avoid the first-pass effect, melatonin microneedles have been prepared to enable transdermal administration of melatonin, which is expected to improve its bioavailability; at the same time, microneedles are suitable for elderly people who cannot take the drug orally. CD Formulation provides melatonin ...
Manufactured by:Quay Pharma based inFlintshire, UNITED KINGDOM
We are extensively involved in developing early clinical formulations and clinical manufacturing of First in Human trials. We can develop a formulation specifically designed to achieve your targets during the crucial first clinical evaluations of your ...
by:Ardena Holding NV based inMariakerke, BELGIUM
At Ardena, we are experts in writing scientific and technical reports using a dossier-centric approach. This means we keep the final dossier submission in mind throughout to ensure consistency, completeness and ...
Manufactured by:CELONIC Group based inBasel, SWITZERLAND
We offer comprehensive Fill & Finish services for liquid-formulated drug products – from aseptic filling to QC tests, labeling, packaging, storage, and release. Our solution-driven GMP-complaint processes come with unparalleled flexibility, fully-adaptable to the unique needs of our clients. ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Long-acting Controlled-release Injection Technologies: CD Formulation can provide our clients with long-acting formulation technologies. Our pharmacologists can provide strategies to extend the duration of action of a drug after injection by (1) modifying the drug structure to extend the half-life of the drug's ...
by:Corpbiz Advisors based inNoida, INDIA
Central Drugs Standard Control Organisation is, known as CDSCO, is a regulatory body for the Indian medical devices industry, under the provisions of the Drugs & Cosmetics Rules, 1945 and Drugs & Cosmetics Act, 1940 and it’s the national regulatory body for Indian pharmaceutical and medical devices. Team Corpbiz will assist you in CDSCO Registration or DCGI approval for your ...
by:Lifecore Biomedical, Inc. based inChaska,, MINNESOTA (USA)
Lifecore has decades of experience, using its proprietary filtration system, filter sterilizing very high viscosity solutions (>100,000 cps sodium hyaluronate solutions) while conforming to industry standards for filter ...
Manufactured by:CELONIC Group based inBasel, SWITZERLAND
ProJect Pharmaceutics* builds quality into formulation and processes and applies high-throughput predictive stability technologies (Predictive Formulation Analytics, PFA) to ensure manufacturing consistency. Using such a regulatory-compliant Quality by Design (QbD) step at an early stage will result in an accelerated and risk-mediated downstream process (DSP) ...