The programme ECA Certified Packaging Manager lets you qualify as a specialist for pharmaceutical packaging systems and packaging operations. It provides guidance on ways to attain best regulatory practice and compliance. In addition, it addresses tools for the efficient and effective development of packaging materials and systems, qualification of suppliers, setting of specifications, management of changes and deviations, and performance of quality control testing.
ECA Certified
Packaging Manager
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 Packaging Manager”.
- Avoiding non-Compliance in Packaging Operations
- Serialization/Aggregation – Dealing with different global requirements
- Leachables & Extractables – Testing & Assessment
- Design Control for Drug-Device Combination Products
- Pharmaceutical Packaging Systems: Development
- Pharmaceutical Packaging Systems: Quality Control
- Plastic/Elastomeric Materials for Pharmaceutical Packaging and Production
- Glass meets Pharma
- GMP for Pre-Filled Syringes (PFS)
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)
(including detailed information on every event – venue, dates, fees and agenda as PDF)
Your Questions
For questions relative to the ECA Certified Packaging Manager, please contact enquiry@gmp-compliance.org.
GMP Conferences by Topics
- General Quality Assurance and GMP Compliance Topics
- Hygiene
- General Microbiology Topics
- Regulatory Affairs
- Development
- General Analytics Topics
- Good Distribution Practice
- Sterile Manufacturing
- Computer Validation
- General Qualification/Validation Topics
- General Engineering Topics
- APIs/Excipients
- GMP Basic Training Courses
- Medical Devices and Combination Products
- Packaging and Packaging Material
- Data Integrity
- Qualified Person (QP)
- GMP Auditing
- Documentation
- Cleaning Validation
- General IT Compliance Topics
- Impurities
- OOS / OOE / OOT
- Material Testing
- Validation of Analytical Methods
- Analytical Instrument Qualification
- Stability Testing
- Microbiological Testing
- Technology
- General Manufacturing Topics
- Solid Dosage Forms/Semi-Solid Dosage Forms
- Biotechnology/Blood/ATMP
- Herbal Drug Products/Cannabis/Radiopharmaceuticals
- Others