CD Formulation services

CD Formulation - API-Excipient Compatibility

CD Formulation can provide you with comprehensive services of API-excipient compatibility, our services can save both time and cost for you by assessing the risk of excipient interactions prior to formulation development. We test the materials that need in the formulation to determine their chemical and physical properties, 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. Our API-Excipient Compatibility Services Obtain an in-depth understanding of physical or chemical API-excipient interactions. Support the selection of the most appropriate excipients in dosage form design. More at https://www.formulationbio.com/api-excipient-compatibility.html

CD Formulation - Crystallinity Determination

CD Formulation can provide you with crystallinity determination services of active pharmaceutical ingredients, 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. Our Methods for Crystallinity Determination Differential scanning calorimetry (DSC) FT-Raman spectrometry X-ray powder diffraction (XRPD) Near infrared spectroscopy (NIRS) More at https://www.formulationbio.com/crystallinity-determination.html

CD Formulation - Amorphous Content Determination

CD Formulation laboratories can test products of any scale, and we can provide comprehensive amorphous content determination for APIs according to related standards. 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. More at https://www.formulationbio.com/amorphous-content-determination.html

CD Formulation - Hygroscopicity Evaluation

CD Formulation laboratories can test products of any scale, and we can provide comprehensive hygroscopicity evaluation for APIs according to related standards. By determining whether APIs are sensitive to moisture, 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. Our Methods for Pharmaceutical Hygroscopicity Evaluation Gravimetric Sorption Analysis (GSA) Method Thermogravimetric Analysis (TA) More at https://www.formulationbio.com/hygroscopicity-evaluation.html

CD Formulation - Particle Size Analysis

The particle size distribution of active ingredients and excipients is an important physical property of materials used to manufacture pharmaceutical products. The size, distribution and shape of the particles will affect the overall performance, stability and appearance of the final product. Therefore, particle size monitoring is essential for the entire drug development and manufacturing process. CD Formulation can provide comprehensive particle size 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.

CD Formulation - Moisture Content Determination

CD Formulation can provide you with moisture content determination services of APIs and inactive ingredients, 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/moisture-content-determination.html Moisture Sources of Dosage Forms Bulk drug Manufacturing processes Inactive excipients Environmental conditions

CD Formulation - Heavy Metal Testing Services in Pharmaceuticals

The professional team of CD Formulation has the expertise and equipment to test and analyze heavy metals in samples to determine whether the drug meets the specified requirements. Among many metals, lead is the most easily introduced heavy metal element, and it is very easy to accumulate in the body and cause toxic reactions, so lead is often the main object of testing. The heavy metal ions react with the chromogenic agent to produce insoluble heavy metal sulfide particles, and compare the color shades of the heavy metal sulfide particles generated by the test solution and the standard lead solution evenly mixed in the solution to determine whether the limit of heavy metals in the test product is in accordance with the regulations. Learn more at https://www.formulationbio.com/heavy-metal-testing-services-in-pharmaceuticals.html.

CD Formulation - Elemental Impurities Analysis

CD Formulation laboratory is cGMP-compliant and equipped with state of the art analytical instruments. We have experienced analysis experts who can work with our formulation and manufacturing team to provide you with drug elemental impurities analysis services. Our elemental impurities analysis is performed in accordance with pharmacopeia methods to give you reliable, independent data, which can help you to make an appropriate risk assessment for your final drug products. In addition, we are also able to develop and validate tailored methods of elemental impurities analysis that will meet your specific needs.

CD Formulation - Long-Term Accelerated Shelf-Life Testing

Long-term accelerated shelf-life testing is performed in artificial environments where the temperature and humidity exceeds normal conditions of sale and consumption. After accelerated aging testing, the product must be subjected to the necessary physical, microbiological and chemical analyses to ensure that we have prior knowledge of the product's stability. CD Formulation offers rapid aging testing in medical products performed as accelerated aging testing. According to the standard, the rapid aging time is calculated based on the product's construction and packaging characteristics, taking into account the temperature and real-time shelf life that the product can withstand. Learn more at https://www.formulationbio.com/long-term-accelerated-shelf-life-testing.html

CD Formulation - Infrared Absorption Spectrometry Analysis of Pharmaceutical Preparations

Infrared spectroscopy is simple and fast, however, for some drugs with different crystalline forms and the same or little difference in infrared spectra, it is difficult to distinguish the infrared spectra, and sometimes the difference in the spectra may be due to the lack of sample purity, the size of the crystals, the transfer of crystals in the grinding process, etc., resulting in deviations in the analytical results. This is when other methods are needed to jointly determine the crystalline form of the sample at the same time. Our skilled scientists at CD Formulation use state-of-the-art infrared (IR), near infrared (NIR) and Raman spectrometers for solid state analysis. Learn more at https://www.formulationbio.com/infrared-absorption-spectrometry-analysis-of-pharmaceutical-preparations.html