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Analytical Chemistry We will provide our valued customers with analytical chemistry research and quality control services for NCEs throughout their life cycle from the early clinical stage to commercial manufacturing.

We will provide our valued customers with analytical chemistry testing services research and quality control services for NCEs throughout their life cycle from the early clinical stage to commercial manufacturing. Analytical Method Development and Validation Guided by Quality by Design (QbD), we provide comprehensive analytical method development and validation in accordance with ICH Q2 based on Critical Quality Attributes (CQA) to support oral dosage form development. We also perform life cycle management to ensure quality research and control and provide accurate and reliable data at different drug development stages.

The microwave reaction system is a microwave accelerated reaction system with chemical reaction process control. The control, display and operating system are integrated.It has a reliable anti-corrosion design and saves space. At the same time, the instrument has multiple functions and can be used for sample digestion in analytical chemistry, extraction, proteolysis, concentration, drying, organic/inorganic synthesis of experimental chemistry, and chemical process simulation data condition pilot test and other microwave chemistry applications.

After completing molecule's basic benchwork and characterization, it is time to leverage powerful simulation software for in vitro-in vivo extrapolation. Integrating in silico advancements into program will help consumer expedite timeline for CMC (chemistry, manufacturing, and controls) and dosing strategies. We can identify absorption risks in the early development and optimize preclinical and clinical dosing strategies.

We will provide our valued customers with analytical chemistry testing research and quality control services for NCEs throughout their life cycle from the early clinical stage to commercial manufacturing. Analytical Method Development and Validation Guided by Quality by Design (QbD), we provide comprehensive analytical method development and validation in accordance with ICH Q2 based on Critical Quality Attributes (CQA) to support oral dosage form development. We also perform life cycle management to ensure quality research and control and provide accurate and reliable data at different drug development stages.

Analytical Chemistry - Crystal Pharmatech Co., Ltd.

Highlights of API Form and solid state services Serving over 1000 clients worldwide Supported solid form screening, crystallization, and preclinical formulation development of over 2,000 new drug molecules The world's leading technology supports the understandingof molecule and formulation with a high-end platform High-quality service, a culture of confidentiality, and fast turnaround with cost-effective pricing Customized solution for your molecule, spanning the entire drug lifecycle API Form and solid state chemistry services Solid Form Screening and Selection Solid form is a general term that refers to both crystalline and amorphous materials. The solid form will impact active pharmaceutical ingredient (API) development properties such as solubility, dissolution rate, stability, hygroscopicity, and bioavailability.