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Drug Stability Services
24 services found
by:MtoZ Biolabs based in, MASSACHUSETTS (USA)
Drug affinity responsive target stability is a label-free small molecule probe technique under chemical proteomics first proposed by Lomenick et al. in 2009, which makes it possible to track and identify target proteins whose stability changes after binding with small molecules. To date, Drug affinity responsive target ...
by:MtoZ Biolabs based in, MASSACHUSETTS (USA)
Biopharmaceutical stability analysis is crucial for assessing the safety, efficacy, and quality of biopharmaceuticals throughout their storage, transportation, and usage. This analysis evaluates changes in the chemical, physical, microbiological, and biological properties of the ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
CD Formulation offers Mandatory Degradation Tests that help customers find ways to promote drug stability. Our end-to-end enhancement solutions combine complete capabilities from concept to commercialization, minimizing project complexity, timelines, and ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
Influencing Factors Analysis: Influence factors test is conducted under drastic conditions, its purpose is to understand the factors affecting drug stability and possible degradation pathways and degradation products, to provide a basis for the prescription, process, packaging, storage conditions, transportation, use and expiration date / retest period ...
Manufactured by:CD Bioparticles based inShirley, NEW YORK (USA)
CD Bioparticles offers custom services to characterize drug stability. For recent years, our experienced scientists have been dedicating ourselves to helping every custom to measure drug stability when bioparticle formulation is ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
About 40% of newly developed medicinal chemical entities have poor water solubility, and 90% of drugs under development can be classified as poorly soluble drugs. A solid dispersion (SD) refers to a dispersion system in which the drug particle size is within the range of 0.001 to 0.1 μm in a certain state and uniformly dispersed in a solid ...
by:Solvias AG based inKaiseraugst, SWITZERLAND
We understand that early assessment of a protein biopharmaceutical’s stability can be invaluable, even during pre-development. For drug substances and drug products all stability aspects can be monitored including long term and accelerated stability studies, in use studies, short term temperature excursion ...
Manufactured by:CD Formulation based inShirley, 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, ...
by:Niracle, LLC. based inNewtown, PENNSYLVANIA (USA)
Examples include content uniformity related failures, dissolution problems, polymorph conversions during manufacturing and stability studies, drug release related issues for prolonged release formulations, and problems related to fluid-bed wet granulation ...
Manufactured by:RheaVita based inGent, BELGIUM
During freeze-drying, biopharmaceutical and other products require protection against dehydration stress during freeze-concentration and drying. Therefore, a suitable formulation strategy is essential to guarantee the long-term stability of drug products. This strategy could include adding protectants to withstand the dehydration stress, selecting a suitable ...
Manufactured by:Biodextris based inLaval, QUEBEC (CANADA)
Clinical Drug Substance/Product Analysis: We support you to confidently release your clinical product by executing validated assays which form the backbone of your product monograph or IND CMC section, and establish the quality, efficacy and safety of your product. Our technologies allow complete analysis of bulk drug substance and liquid or lyophilized drug product, and the validated analytical ...
by:MtoZ Biolabs based in, MASSACHUSETTS (USA)
HCP is a critical quality marker in the development and production of bioproducts, particularly recombinant protein drugs. Its presence can impact drug purity and stability and may trigger adverse immune responses. Thus, qualitative identification and relative quantification of HCP are essential in drug development and quality ...
Manufactured by:ABX Advanced Biochemical Compounds GmbH based inRadeberg, GERMANY
The focus is on finding optimal radiochemical labelling conditions using various radionuclides such as F-18, Ga-68, Lu-177, and I-123. This development involves meticulous purification and formulation to create a reliable drug product. The process includes stability and formulation studies to ensure a safe and stable solution for patients. With a facility housing ...
by:MtoZ Biolabs based in, MASSACHUSETTS (USA)
In biopharmaceutical processes, particularly for protein and antibody drugs, charge heterogeneity analysis is crucial for ensuring quality control of bioproducts. Interactions between molecules with different charge can significantly impact the bioactivity, immunogenicity, half-life, and charge stability of drugs, ultimately affecting their ...
by:MedPharm Ltd. based inDurham, NORTH CAROLINA (USA)
Analytical and bioanalytical methods underpin all the services MedPharm provides and we have dedicated experts to ensure we can solve the most complex of challenges and stay at the forefront of the ...
Manufactured by:Relequa Analytical Systems Ltd based inDungarvan, IRELAND
Relequa's Moisture Profiling™ is an advanced method specifically designed to measure moisture movement in pharmaceutical products, providing precise insights into their stability. Unlike conventional techniques like Loss-on-Drying or Dynamic Vapour Sorption, which rely on weight metrics, Moisture Profiling measures moisture status changes due to water vapor exchange. This ...
Manufactured by:Piramal Pharma Solutions (PPS) based inMumbai, INDIA
In vitro facilities at PDS provide absorption, distribution, metabolism, and excretion (ADME) services for faster and improved decision making points or standalone offering to support drug discovery programs. Cost-efficient, standardized and customized assays for ADME parameters are provided to the ...
Manufactured by:Piramal Pharma Solutions (PPS) based inMumbai, INDIA
The highly experienced analytical development team covers a wide range of analytical methods from small molecule analysis through to cell killing assays and ELISA development. We support the analytical development, validation, and quality control release testing needed to get ADC or bioconjugate to clinic or market, all at one location. We also offer method development and testing to characterize ...
Manufactured by:Ascendia Pharmaceuticals based inNorth Brunswick, NEW JERSEY (USA)
Nanotechnology is now being extensively utilized in the development of innovative drug delivery systems for various routes of administration. Due to the advantages of their targeted drug delivery, reduced toxicity, long circulation, and enhanced half-life, nanoparticles are particularly useful for use in long acting formulations. Different types of injectable nanomedicines have been ...
Manufactured by:Creative Bioarray based inShirley, NEW YORK (USA)
Creative Bioarray provides various in vitro ADME/PK services including high-throughput ADME screening, in vitro metabolism, in vitro permeability and transporter assays. ADME is short for "absorption, distribution, metabolism, and excretion". The four properties determine the drug level within a body, the drug exposure to tissues, and the metabolic process of a compound, which can help predict ...