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Pharmaceutical Microbiology Testing Articles & Analysis
14 news found
The Food and Drug Administration’s (FDA) recent Roadmap to Reducing Animal Testing in Preclinical Safety Studies marks a pivotal shift toward the adoption of innovative, human-relevant methodologies commonly known as New Approach Methodologies (NAMs). As leaders in preclinical research tools, we welcome this movement towards advanced and validated NAMs solutions already in place. emka ...
As the new academic year looms on the horizon, CD Formulation is ecstatic to announce a special Back to School Promotion 2024. Emphasizing its commitment to supporting educational and research institutions, the promotion offers up to 10% off on all their products and services. This timely initiative aims to facilitate ground-breaking research and innovation in pharmaceutical, cosmetic, and ...
CD Formulation, a CRO service provider of analysis and testing services, offers a comprehensive range of tests for determining physical parameters in pharmaceutical formulations. These tests play a crucial initial role in ensuring the quality, stability, and efficacy of pharmaceutical products. One of the key tests offered by CD Formulation is the relative density test. This test determines the ...
In the ever-evolving field of pharmaceuticals, CD Formulation has emerged as a major player in developing innovative drug delivery systems aimed at enhancing the efficacy and safety of therapies. Through its expertise in various cutting-edge technologies such as microneedle and thin film technologies, transdermal patches, microencapsulation, and nanoparticle development, CD Formulation is ...
In the pharmaceutical industry, ensuring product safety and efficacy is paramount. Therefore, rigorous testing and analysis procedures are employed to ensure that pharmaceutical products meet the required standards. CD Formulation is emerging as a trusted partner specializing in biological determinations for pharmaceutical analysis and testing. From sterility testing to disinfection efficacy ...
The need for high-quality pharmaceutical development services has never been more pressing. Therefore, in a swift response to such demand, CD Formulation has recently rolled out its new Pharmaceutical Formulation Characterization Testing (PFCT) services, a move aiming to help ensure that the newly developed pharmaceutical products are stable, effective, and in compliance with the regulatory ...
Pharmaceutical testing is a must to ensure that all medications meet the top quality, safety, and performance requirements before they enter the market. CD Formulation’s cGMP-compliant laboratory is well-equipped to identify both the chemical and structural composition of each drug substance. More recently, the company announced to broaden its service range to tablet fragility test, ...
Packaging is another factor that decides the stability and integrity of drugs. Except for the role as an excipient producer and supplier, the US-based CRO company CD Formulation today announces that it newly launches a wide range of pharmaceutical packaging services, providing support throughout the whole process of packaging design, from material selection to chemical and surface analysis and to ...
Earlier this month, CD Formulation announces that it is now capable of providing nitrosamine impurities analysis service for customers who are involved with drug formulation projects and need help from CRO companies like CD Formulation. The analysis of nitrosamines can be challenging. These ultra-low levels of impurities must be quantified in a variety of complex matrices. Equipped with all the ...
In a recent statement, the York-based CRO company CD Formulation announces the launch of tailored solutions for increased bioavailability excipients, which aims to tackle the issue of poor bioavailability, a long-lasting challenge in drug development. Many drug candidates unfortunately stopped their way ahead from the discovery pipeline just simply because they are poorly water-soluble, which ...
Titration is an important analytical method that is widely used for pharmaceutical assay testing. However, many USP monographs still refer to manual visual endpoint titration methods. Such manual procedures are not only tedious to perform but also more prone to human error. A free white paper by Metrohm summarizes the steps involved converting an existing manual titration procedure to ...
Oxford Brain Diagnostics has started a project for Takeda Pharmaceuticals. The project is testing Cortical Disarray Measurement (CDM®) technology as a neurodegeneration biomarker with a view to using it in future clinical trials. Dr Steven Chance, CEO, said ‘we are very excited to be engaged with Takeda on this project using our CDM method on diffusion MRI scans. Alzheimer’s ...
Near-infrared spectroscopy (NIRS) has long been one of the most versatile analytical techniques in the pharmaceutical and other industries as it can handle any sample matrix, requires no sample preparation at all and provides real-time results for multiple parameters at the push of a button. The latest applications developed by Metrohm are dedicated to the pharmaceutical, polymer, and other ...
Health authorities reported that a tainted dye and injection used during eye surgeries caused 33 cases of rare fungal eye infections. The products were made by the same Florida pharmacy, Franck’s Compounding Lab, that produced the supplements responsible for killing 21 elite polo horses in 2009. All patients with the infections had undergone either eye surgeries or injections. According ...