Most audit findings start in the grow room. I find them there.
GACP and EU-GMP readiness for pharmaceutical-cannabis facilities. I read your rooms and your records together — and fix each finding where it starts.
The auditor cites the paperwork. The cause is in the room.
Illustrative examples. Every findings log I issue carries both columns.
Room-to-Record Inspection
One day on-site. A findings log graded Critical, Major and Minor, each tied to its clause and its room. $2,500 fixed plus travel at cost — credited in full if you start a programme within 60 days.
“Very knowledgeable across every type of certification — the right person to build a QMS, maintain it and keep it sustained.”
Four situations I get called into.
You can't export without a certificate
Licensed, well grown — and a buyer who won't move without GACP.
You failed an audit
Open non-conformances and a contract waiting on the outcome.
You're still building
Designing compliance in now costs a fraction of retrofitting it.
You import and need to trust the farm
I audit your supplier's rooms and records and tell you what the certificate doesn't.
Fixed where it starts. Held by your own team.
1 · A two-column findings log
Each gap graded, cited to its clause and traced to where it starts.
2 · A corrective plan
Owner and deadline per finding, tracked to close — on the room as well as the record.
3 · A QMS your team can run
Handed over through mock audits and SOP walkthroughs, then support through the certification audit.
Billed by milestone, with each stage's deliverables agreed in writing before it starts.
A grower who reads Annex 7.
I ran commercial grow rooms for twenty years before I started auditing them. So I read a drying-room log and a micro result as one problem, not two — the link a pure document reviewer misses.
And if your facility isn't ready, I'll tell you before the audit, not after it.
- 2026–27Postgraduate Diploma, Pharmaceutical Quality Systems — IL3, Universitat de Barcelona (in progress)
- 2025ECA Academy — GMP-Compliance Manager — CAPA, ICH Q9, supplier qualification
- 2025European QP Association · ECA GMP Pharma Congress
One quality system across the standards you need.
The questions I get asked first.
How long does certification take?
Do you issue the certificate?
BioCompliance is part of Hydrofarm. Will you push their equipment?
Are you insured, and who owns the work?
Book a free 20-minute call.
Tell me what you grow, where you want to sell it and which certificate is blocking you. I'll tell you how far off you are — and if you don't need me, I'll say so. Replies within one business day.
Prefer to write? Send me a note instead.