by Jill Ellsworth | Sep 2, 2026 | Infusion & Product Formulation
Cannabis infusion process capability is the easiest way to answer the question you eventually hear from QA, operations, or a buyer: can you reliably hit label claim, batch after batch, without holding your breath until the COA comes back? If you run infused pre-rolls,... 
by Jill Ellsworth | Aug 24, 2026 | Decontamination & Microbial Safety
Your ozone decontamination run log is the one page that answers a simple question: did this cycle actually run the way your SOP says it runs? If you have ever prepped for an inspection, you already know the vibe. Your SOPs are organized, training records are signed,... 
by Jill Ellsworth | Aug 20, 2026 | Infusion & Product Formulation
Infusion equipment total cost is the number that decides whether your infusion line runs calmly or keeps you chasing problems between batches. The quote you get from a vendor is only the opening line. The real spend usually hides in labor, cleanup, changeovers,... 
by Jill Ellsworth | Aug 17, 2026 | Compliance, QA & Testing
Digital batch records cannabis teams rely on can be the difference between an audit that feels routine and one that drags your whole week into the weeds. If your batch story lives on paper, in binders, or across a few “temporary” spreadsheets, you know the drill: you... 
by Jill Ellsworth | May 19, 2026 | Industry Insights & Technology
The future of cannabis QA is moving fast, and having predictive analytics baked into your process will give you a serious edge. As someone who’s been part of this industry right through its ups and downs, I’ve seen first-hand how prevention-first...