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CURRICULUM

Training Programs

Training for Professionals

Course Overview

This program is designed to support employees in the pharmaceutical and biotechnology industries by enhancing their job competencies, facilitating career transitions, and building networks. It consists of open-enrollment courses and customized corporate courses.

Open
Enrollment

This is an open training program where individuals can participate by registering for the open training program.

Customized Training

This is a closed training program designed and operated to meet the specific request of a company.
※ Programs can be configured in various formats such as 2-3 days or 5days. For more details, please inquire through the 1:1 inquiry channel.

Curriculum

Classification Contents
Cultivation

Classification Structure and Principles of Bioreactors and Centrifuges

  • Multi-use bag assembly and disassembly
  • Pilot fermenter structure and P&ID practice (Inoculation, Sampling, Harvesting)
  • Lab fermenter inoculation (Transformation (E.coli+ plasmide))
  • Explanation of the relationship between utilities and pilot fermenter parameters
  • Centrifugation: Comparison of tubular, disk stack, and laboratory rotor methods
  • 5L fermenter harvesting, operation of a labortory centrifuge, and 5L culture pellet harvesting
  • Cell Disruption: Operation of the Homogenizer
Purification

Classification Purification Processes: Understanding AKTA and TFF Systems

  • Chromatography Resin Fundamentals & Selection
  • Chromatography Theory (Ion Exchange, Hydrophobic Interaction, Affinity, Size Exclusion Chromatography)
  • Effective Purification Process Design
  • Chromatography Practical Training
  • Fundamentals of Filtration
  • Application of TFF (CFF) in Bioprocessing
  • TFF(CFF) Principles & Practical Training
QA

Classification Investigation Method & Technique for Deviation Investigator

  • Investigation Process
  • Defining the Problem of a Deviation: Writing a Deviation Occurrence Report
  • Data Collection for Problem-Solving: Interviewing Techniques
  • Identifying and Analyzing Root Causes: Utilizing Investigation Tools
  • Establishing an Effective CAPA
QC

Classification Quality Control: Understanding Capillary Elecrophoresis and Endotoxin Testing

  • Sample and Mobile Phase Preparation
  • Explanation and Setup of Capillary Electrophoresis
  • Post-Run Data Analysis
  • Calibration Curve Reliability
  • Preliminary Test for Reaction-Interfering Factors
  • Endotoxin Quantification