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Waters-BioInfra ASEAN Academy for Bioanalysis

우리는 아세안국가들과의 동반적 발전을 추구합니다.
우리의 기술과 경험이 필요하다면 기꺼이 공유하겠습니다.

  • 아세안 아카데미 문의

    담당부서 : 아세안 아카데미
    전화 : +82-31-627-2800
    E-mail : academy@bioinfrakorea.co.kr

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  • 워터스-바이오인프라 아세안 아카데미는 아세안국가 분석연구원들의 분석기술 연수를 위해 워터스와 바이오인프라가 공동으로 운영하는 교육시설입니다.
  • 교육시설은 바이오인프라가 무상으로 제공하며 바이오인프라 본사에 설치되어 있습니다.
  • 실습용 분석기기는 워터스가 무상으로 제공합니다.
  • 아카데미 개소식

    아카데미 개소식

  • 연구실

    연구실

  • 강의실

    강의실

  • 실험실습실

    실험실습실

  • 실습용 분석장비

    실습용 분석장비

  • 실습용 로봇

    실습용 로봇

  • 해외연수생 숙소(침실)

    해외연수생 숙소

  • 해외연수생 숙소(화장실)

    해외연수생 숙소

Curriculum

  • Training Contents
  • 1 Chromatography and Molecular Detection
  • 1-1 Introduction of Chromatography
  • 1-2 Introduction of Detectors
  • 1-3 Operation of LC-MS/MS
  • 2 Establishment of a LC-MS/MS Detection
  • 2-1 Selection of Mass Tune Parameters
  • 2-2 Screening of LC Condition Using Grdient Technique
  • 2-3 Modification of the LC Condition
  • 3 Experimental Error Control
  • 3-1 Definition of Terms related to Error
  • 3-2 Significant Figures and Weighing
  • 3-3 Liquid Handling Error and Selection of Apparatus
  • 3-4 Correction of Measurement Error by Stable Isotope IS
  • 3-5 Check of Adsoption and the Prevention
  • 4 Stability and Stabilization
  • 4-1 Reaction Order and the Catalist
  • 4-2 pH-Stability and Selection of the pH-Range
  • 4-3 Temp-Stability and Selection of the Storage Temp
  • 4-4 In vitro metabolism and stabilization
  • 5 Extraction Methods
  • 5-1 Protein Precipitation
  • 5-2 Liquid-Phase Extraction
  • 5-3 Solid-Phase Extraction
  • Training Contents
  • 6 Design of an Analytical Method and the Preliminary Test
  • 6-1 Design of an Analytical Method
  • 6-2 Check of Extraction yield, Matrix Effect and Cross-Talk
  • 6-3 Modification of the Designed Method
  • 6-4 Preliminary test of the Modified Method
  • 7 Bioanalytical Method Validation Study 1
  • 7-1 Design of MV Study based on ICH M10
  • 7-2 Preparation of the MV Protocol
  • 7-3 Short-Term MV Studies
  • 8 Bioanalytical Method Validation Study 2
  • 8-1 Long-Term Stability Test
  • 8-2 Preparation of the MV Report
  • 8-3 Design of Partial and Cross Validation Studies
  • 9 Study Sample Analysis Using a Validated Method
  • 9-1 Preparation of Study Sample Analysis Plan
  • 9-2 In-Site Validation of the Method
  • 9-3 Study Sample Analysis
  • 9-4 Incurred Sample Reanalysis and Reporting
  • 9-5 Preparation of Study Sample Analysis Report
  • 10 Advanced Lab Systems
  • 10-1 Laboratory Information Management System
  • 10-2 Environment Monitoring Systems
  • 10-3 Lab Robotics
  • 10-4 Automated Data Processing and Reporting System
  • Training Contents
  • 11 GCLP Standards and Study Conduct
  • 11-1 Introduction of GCLPs
  • 11-2 Contract and Clinical Trial
  • 11-3 Sample Management and Analysis
  • 11-4 Sample Labeling, Receipt, Storage and Chain of Custody
  • 11-5 Preparation and Distribution of Clinical Kits
  • 11-6 Method Validation
  • 11-7 Repeat Analysis
  • 11-8 Data Recording
  • 11-9 Blinding/Unblinding
  • 11-10 Reporting
  • 11-11 Discussion
  • 12 Laboratory Operation
  • 12-1 Standard Operating Procedures (SOPs) and Facility Policies
  • 12-2 Organization
  • 12-3 Personnel
  • 12-4 Facilities
  • 12-5 Equipment Maintenance
  • 12-6 Computerized Systems
  • 12-7 Quality Assurance Processes
  • 12-8 Quality Control
  • 12-9 Retention of Data