95 services found
CD Formulation services
CD Formulation - Preformulation
Preformulation is an investigation of physical and chemical properties of a drug substance when used alone or combined with excipients. Early prediction of these properties will generate information useful to the formulator in developing stable and safe dosage forms with good bioavailability.
At CD Formulation , our preformulation services are equipped with advanced instrumentation, and our research team not only have the expertise to handle the most complex formulations, but also have a depth of experience in the pharmaceutical industry and contract service organisations. CD Formulation can offer tailored and rational preformulation development.
https://www.formulationbio.com/preformulation.html
CD Formulation - LogP/LogD/pKa Analysis
CD Formulation can provide you with LogP/LogD/pKa analysis services of APIs and inactive ingredients, and the pKa testing will be performed by our scientists through calculating the LogP or LogD values and measured in various pH values. It will help you to make a decision for operational and procedural conditions that can ensure the physical and chemical stability and pharmacological activity of the product to minimize potential formulation and stability issues. More at https://www.formulationbio.com/logp-logd-pka-analysis.html
CD Formulation - Solubility Analysis
CD Formulation can provide you with dissolution profiles of active pharmaceutical ingredients in various solvents (including inorganic solvents with different pH values, organic solvents, simulated intestinal juice or gastric juice, and other solvents) according to your needs. In addition, our scientists specialize in providing solubility enhancement services through a variety of technologies and methods to minimize potential formulation and stability issues. Learn more at https://www.formulationbio.com/solubility-analysis.html
Our Solubility Analysis Services
Building a full range pH solubility profile
Solubility in simulated gastrointestinal media
Solubility improvement
CD Formulation - Stability Analysis
Stability analysis is a very interesting field in pre-formulation research. Under the influence of various environmental factors (such as temperature, humidity, and light), the stability of active pharmaceutical ingredients (API) or the stability of pharmaceutical products is evaluated. This is helpful to study the internal stability of candidate drug molecules and obtain useful information, it is important to improve the integrity of pharmaceutical products and prevent changes in their physical, chemical and pharmacological properties. CD Formulation can provide you with stability analysis services of active ingredients and excipients, and our scientists will help you to make a decision for operational and procedural conditions that can ensure the physical and chemical stability and pharmacological activity of the product to minimize potential formulation and stability issues. Learn more at https://www.formulationbio.com/stability-analysis.html
CD Formulation - Solubility Improvement and Bioavailability Enhancement Services for Drug Design
Bioavailability refers to the degree and speed at which a drug is absorbed into the blood circulation. There are ongoing challenges with poorly water-soluble drugs and have failed to reach the market due to their poor water solubility. CD Formulation has developed a range of technologies and formulation expertise to improve the solubility and bioavailability of these drugs, helping customers find the right way to commercialize their drug products. This experience, along with a variety of techniques, enables CD Formulation to overcome many of the hurdles surrounding solubility and bioavailability, including physical, chemical, encapsulation techniques and so on. Learn more at https://www.formulationbio.com/solubility-improvement-and-bioavailability-enhancement-services.html
