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Hefei KS-V Peptide Biological Technology Co., Ltd. Hefei KS-V Peptide Biological Technology Co., Ltd.
Hefei KS-V Peptide Biological Technology Co., Ltd.
Preclinical Research

KS-V peptide is a contract research organization (CRO), relying on the platform of Suzhou Research Institute, we provide customers with customized preclinical service plans, including drug metabolism, pharmacokinetics, efficacy studies, and toxicology. We provide customers with high-quality data and a fast turnaround time to support their drug development, preclinical research, and clinical research and help them choose the most valuable drug candidates to enter the clinical trial stage. Our pre-clinical research services include three main parts: pharmacokinetics, pharmacology, and drug safety assessment. Our pre-clinical research services cover all aspects, including design, in vivo research, sample analysis, professional data analysis, IACUC review, and preparation of application materials.


Choose KS-V Peptide Preclinical Research

KS-V Peptide has nuclear magnetic resonance (NMR), gas chromatography-mass spectrometry (GC-MS), liquid chromatography-triple quadrupole mass spectrometry (LC-MS), inductively coupled plasma emission spectrometry (ICP-OES), inductively coupled plasma mass spectrometry (ICP-MS), high-performance liquid chromatography (HPLC), gas chromatography. There are dozens of high-end detection instruments and equipment, such as GC, elemental analyzer, ion chromatography, automatic dissolution instrument, microwave digestion/extraction system, etc., which have passed the National Laboratory Metrology Certification (CMA). Based on these advanced facilities and equipment, the company now has a technical platform to undertake reverse analysis of reference preparations, trace impurities analysis, compatibility study of pharmaceutical packaging materials, genetic toxicity impurities research, pharmaceutical quality research and other detection analysis and research and development.

The main research directions include reverse engineering of preparations, analysis of raw materials and accessories, development of prescription technology, the study of genotoxic impurities, compatibility of packaging materials, and large-scale instrument testing.

The center has three senior experts in pharmaceutical research, analysis and testing, and system certification. At the same time, two well-known professors in the industry are employed as special technical guidance to provide a decision-making basis and technical guidance for key research projects. Other project managers and technical backbone are responsible for the implementation of daily experiments and the verification of data reports. Front-line experimental technicians are bachelor's degrees or above, familiar with various detection methods and procedures. Senior expert tutors and hard-working project managers form the backbone of the center. In addition, the decision-making level of the research institute is familiar with the whole work process and has a deep understanding of the relevant compliance and technical requirements, thus ensuring the complete implementation, quality and quantity of each project undertaken.

Up to now, the center team has undertaken a number of generic drug Commission declarations, research and development, consistency evaluation, compatibility research of pharmaceutical packaging and testing services in the health field such as food and medicine, and has established good cooperation with domestic industry, academia and government departments.