Frank Zhang

Business Development Manager at Adicon Clinical Laboratories, Inc.
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Contact Information
us****@****om
(386) 825-5501
Location
Shanghai, China, CN

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Experience

    • Business Development Manager

    • Medical Practices
    • 1 - 100 Employee
    • business development manager
      • Jan 2004 - Present

      ADICON Central Lab About Adicon Adicon Clinical Laboratory, Inc. (www.adicon.com.cn) is a leading full-service independent clinical lab in China. Currently, we are operating thirteen labs located in Shanghai, Beijing, and Hangzhou etc. We are intending to build a national network with more than twenty labs throughout the country before 2012. We dedicates to serve the central testing of clinical trials and clinical lab testing, Adicon Central Labs To meet the diversified needs of pharmaceutical client for new drug development, Adicon had made its Central Labs to international standards in Shanghai. With over 1000 assays currently available, ADICON Central Lab provides testing services for Routine, Biochemistry, Trace element, Molecular Biology, Immunology, Microbiology, Pathology,HA1c, Coagulation, and R&D. Services • Provide a wide range of professional testing services with CAP standard for clinical trials. • Provide project management service. • Provide data management and query delivery. • Provide logistics services in China. • Provide specimen storage services under -20℃ or -70℃ condition for long term. Quality Since 2004, Shanghai Adicon successfully received College of American Pathologists (CAP) Certificate, National Glycohemoglobin Standardization Program (NGSP) Certificate, Metrology Accreditation Certificate, etc. Project Management We provide a certificated project manager and a management team with good clinical research background for each project. The service of project management contains investigator training and management, kit management, document management, risk management, logistic management, sample management and close out. Data management We set up MS SQL and Oracle Database System, Central Lab Management System, SOPs, and records comply with ICH GCP, US FDA 21 CFR Part 11 requirements. Electronic Format of Testing Data including HL7, XML, ODF, Excel, TXT, PDF, etc. Show less

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