What we do
- EU GMP fundamentals
- GACP for cultivation teams
- GDP for distribution teams
- Good documentation practice
- Data integrity and ALCOA+
- Root cause analysis and CAPA
- Quality risk management
- Internal auditor training
- AI in GMP and draft Annex 22
How it runs
- 01
Needs
We agree with you who attends, which roles they hold and what they need to be able to do.
- 02
Course
We hold the course on site or online, on the dates agreed with you.
- 03
Records
Each participant ends with a learning check, and you receive the training records for your files.
Other services
- Importing flower or extracts into the EUEU GMP supplier qualification
- Auditing a supplier, a CMO or your own siteIndependent EU GMP and GDP audits
- Growing cannabis for medical useGACP cultivation compliance
- Selling to EU GMP buyersFrom GACP to EU GMP
- Building or fixing your quality systemPharmaceutical Quality System
- Running quality without a QA teamFractional QA
Read more
- What does draft Annex 22 allow an AI assistant to do in GMP software?Draft Annex 22 keeps generative AI out of critical GMP applications, so what an assistant may do depends on where its output ends up.Read the article
- First-party or second-party audit: which one do you need?One looks inward at your own quality system, the other looks outward at your suppliers. EU GMP expects both, and neither can stand in for the other.Read the article
