Medidata, the world's leading provider of cloud solutions for life sciences, announced today that it has partnered with China's clinical development services and solutions provider, Pulse Biomedical Technology (Shanghai) Co., Ltd. (hereinafter referred to as “Jianmaiâ€). The company will use the Medidata cloud platform to promote operational efficiency and growth in its clinical development in China.
Media has leveraged Medidata's world-leading collection, management and reporting patient data solution, Medidata RaveTM, and Medidata BalanceTM, which combines randomized distribution and trial supply management (RTSM) and electronic data collection (EDC) into one system. Save time in data management and strengthen the quality of trials in major early studies. In addition, the company will also use the Medidata Rave Research Design and Construction Essentials (SDBE) training course and the Associated Instructor Training (SDBE TTT) course to provide the research team with the basic knowledge of research management and maintenance, including electronic medical records. Reporting tables (eCRFs) basic development skills and simple data validation development skills, as well as research design related skills and practices.
Is a clinical contract research organization (CRO) that provides high quality, end-to-end services to biopharmaceutical and medical device companies in China and around the world. It is headquartered in Shanghai. Its services include strategic consulting for clinical development and product registration science; clinical trial design and implementation; clinical data management, biostatistics and programming, medical writing, pharmacovigilance and risk management; and clinical trial quality assurance and review preparation. The data management team of the company has more than 15 years of experience and is very good at using the Medidata platform.
Tangmai Biomedical Technology (Shanghai) Co., Ltd.
Mr. Huang Guiping, Vice President of Operations, Asia Pacific, Medidata, said: “We welcome Lions to become a partner of Medidata. Together with China's leading CRO, we will help us further meet the demand for Medidata's advanced solutions in the Chinese market. We look forward to working closely with the company and supporting the company as a trusted partner in clinical development in China and around the world."
The world's leading provider of cloud solutions provider for life sciences clinical research, Medidata
There are mainly the following parts: 1. Sampling swab with disposable sterile plastic rod/rayon head 2. Sterile sampling tube containing 3ml of virus maintenance solution (gentamicin and amphotericin B are selected to better inhibit the fungus in the sample. Avoid the human sensitization reaction that may be caused by penicillin in the traditional sampling solution.) In addition, there are additional parts such as a tongue depressor, a biosafety bag, etc. Intended to use 1. It is used for monitoring and sampling of infectious pathogenic microorganisms by disease control departments and clinical departments. It is suitable for sampling of influenza virus (common influenza, highly pathogenic avian influenza, H1N1 influenza virus, etc.), hand, foot and mouth virus and other types of viruses. It is also used for sampling of Mycoplasma, Chlamydia, Ureaplasma, etc. 2. It is used to transport nasopharyngeal swab samples or tissue samples from specific parts from the sampling site to the testing laboratory for PCR extraction and testing. 3. It is used to preserve nasopharyngeal swab samples or tissue samples from specific parts for necessary cell culture. The virus sampling tubes are loaded with infectious substances, and some are even highly pathogenic substances. Therefore, the requirements for packaging containers are very strict, and three requirements must be met at the same time: 1. The safety of transportation. Ensure that the sample does not leak during transportation. Sampling tubes that comply with WHO regulations and biosafety regulations. 2. The security of preservation. Ensure that the sample does not leak during storage. Sampling tubes that comply with WHO regulations and biosafety regulations. 3. The validity of the sample. Make sure that the sampling tube itself will not have a toxic effect on the sample.
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