Our approach
Four phases from first walkthrough to ongoing support. Transparent, predictable, built to hand off cleanly to your team when that makes sense.
Week 1
We do a structured on-site or remote walkthrough, map every hazard and regulatory touchpoint, and produce a written gap analysis.
Your team: Ops lead, lab manager, facilities. Minimal bench interruption.
Weeks 2–8
We scope the program you need — not a bloated binder — and write the specific policies, training plans, waste streams, and submittals required.
Your team: Head of Ops, QA/QC, Safety Committee, legal if applicable.
Weeks 3–6
We stand up the program — file the paperwork, run the training, label the containers, install the trackers.
Your team: Entire workforce during training rollout; otherwise minimal impact.
Ongoing
We keep the program alive — inspections, record reviews, renewals, and regulator representation.
Your team: Typically 1 ops counterpart; we handle the rest.
How we work
Everything we produce is specific to your site. No templated binders, no generic checklists, no rebranded exemplars.
Policies and SOPs are written so the people actually doing the work will read and follow them. If your lab tech can't understand it, it isn't done.
Compliance is the floor. The goal is an operation that's safe, defensible, and doesn't slow science down.
When the regulator shows up, you shouldn't be alone in the room. Our engagement fee includes on-site representation.
Start with a free 15-minute review — we'll tell you honestly where you stand and what phase you'd start in.
