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Conferences - GMP Certification Programme


ECA Certified Quality Control Manager


The most frequently cited cGMP non-compliances are often found in analytical laboratories - showing the importance of the pharmaceutical quality control and the Quality Control Manager. Further, the QC Manager has to observe a multitude of GMP requirements (FDA, EMA, WHO, Pharmacopoeias, etc.).

The programme ECA Certified Quality Control Manager lets you qualify as a specialist for analytical GMP laboratories. It provides guidance on ways of attaining best regulatory practice and compliance. In addition, it addresses tools for the efficient and effective management and performance of quality control laboratories today.

This programme will be of significant value to employees both in routine quality control and in analytical development laboratories, who are responsible for GMP compliance and laboratory organisations:

  • Analytical scientists
  • Analytical laboratory managers / supervisors
  • Employees working in the incoming goods control of APIs, excipients, and packaging materials
  • Contract laboratories personnel
  • Auditors responsible for assessing laboratory compliance and performance

"Your Questions"

For questions relative to the ECA Certified Quality Control Manager, please contact

Courses and Conferences acknowledged

To receive the certificate, the applicant must attend three out of the following courses / conferences. After attending the third course, the applicant obtains the certificate "ECA Certified Quality Control Manager".

  • Integrating Analytical Equipment Qualification and Computerised System Validation
  • Maximising HPLC Productivity
  • Quality of Pharmaceutical Packaging Systems
  • Quality Control of Raw Materials
  • Measurement Uncertainty
  • Validation of Analytical Test Procedures
  • OOS/OOE/OOT Results
  • Impurities
  • Dissolution Testing
  • Efficient and Effective Quality Management in the Analytical Laboratory
  • Analytical Data - Interpretation and Treatment
  • FDA Compliance in Analytical Laboratories
  • Reference Standards
  • Analytical Instrument Qualification
  • Plastic Packaging Materials
  • Printed Packaging Materials
  • Setting Specifications
  • Stability Testing
  • Lab Data Integrity
  • Lechables and Extractables

>>> LIST OF ALL COURSES AND CONFERENCES CURRENTLY OFFERED AND ACKNOWLEDGED IN THIS PROGRAMME (including detailed information on every event – venue, dates, fees and agenda as PDF; just click on any event in the list)

 GMP Conferences by Topics
 Quality Assurance
 GMP in Biotechnology
 Regulatory Affairs
 GMP in Pharmaceutical Development
 Quality Control
 Storage, Distribution, Transportation
 Sterile / Aseptic Manufacturing
 Computer Validation
 Technical Operations
 GMP for APIs and Excipients
 Medical Devices
 GMP Basic Training Courses