Service · Compliance Tools

Compliance software built by a compliance professional.

Fixed scope web apps that replace the spreadsheets your quality and regulatory team run on. Specified, built and documented by Wilson Blaney, a former Global Head of Quality with 25 years in GMP & GDP environments, so the tool encodes the regulation correctly first time.

SupplierStatusAudit dueNotes
Rhine Labs GmbHApproved14/03/27TA signed
Kessler Pack LtdPending02/11/26chase audit?
Nordvale Ing.approved??who updated
Bramley Cold Ch.Approved30/01/27temp log v3

Who changed this, and when?

Supplier approval: Rhine Labs GmbH

Approved
Technical agreement
Signed
Audit due
14 Mar 2027
Requalification trigger
Scope change

Audit trail

  • Approved by W. Blaney, 06 Sep 2026 14:12
  • Agreement uploaded by J. Patel, 02 Sep 2026
  • Record created, 28 Aug 2026
25 years in GMP and GDPFormer Global Head of Quality, FTSE 100Responsible Person (GDP) trained860 product novel food dossier led25 years in GMP and GDPFormer Global Head of Quality, FTSE 100Responsible Person (GDP) trained860 product novel food dossier led

Why the spreadsheet is the problem

Most small and mid sized regulated businesses run supplier approval, deviations, training and batch release on spreadsheets and shared drives. They work until an inspector asks who changed a cell, when, and why. Generic software vendors do not understand the regulation, and full GxP platforms cost six figures and take a year to implement. Medicexum sits in the gap: one workflow, turned into a small web app with access control, an audit trail and a data export, in about four weeks.

What we build

  • Supplier approval and qualification tracker

    Approval status, technical agreements, audit due dates and re qualification triggers, aligned to GDP Chapter 5 and GMP Chapter 7, including GDP storage and transport excursions with product impact assessment and disposition.

  • Batch release checklist

    Certificate of analysis review, specification checks and release sign off with a full record of who released what and when.

  • Deviation and CAPA log

    Logging, risk rating, root cause, actions, effectiveness checks and overdue escalation.

  • Training records

    Read and understood tracking against controlled documents, competence sign off and expiry reminders.

  • Novel food product register

    Ingredient, dossier linkage and label claim tracking for CBD and supplement ranges, built from experience leading an RP521 dossier covering 860 products.

  • CBPM importation register

    Import notification tracking, controlled drug register cross reference and licence condition checks for cannabis based medicinal products.

Deviation and CAPA logLive view
RefDescriptionRiskOwnerDueStatus
DEV-0241Cold chain excursion, lane 4MediumJ. Patel18 Sep 2026Open
DEV-0238Label artwork revision missedLowS. Ahmed11 Sep 2026Overdue
CAPA-0117Retrain picking team on FEFOMediumL. Fraser24 Sep 2026In progress
DEV-0235Supplier CoA missing assay resultHighW. Blaney30 Sep 2026Open
CAPA-0114Update goods in SOP for CD receiptLowM. Doyle05 Oct 2026Closed

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Audit trail · DEV-0238

  • Escalated automatically, 12 Sep 2026 09:00
  • Due date set to 11 Sep 2026 by S. Ahmed, 04 Sep 2026
  • Risk rated low by W. Blaney, 03 Sep 2026
  • Record created, 03 Sep 2026

Three ways to start

Free

CBD Compliance Checker

Answer six questions about a CBD product and get a compliance checklist for the UK or EU.

Try the checker
Most clients start here£5,000 to £15,000, fixed price

One workflow as a web app

Scope, build, test evidence, training and handover in about four weeks.

Book a scoping call
From £1,000 a month

Platform and retainer

CannaComply as a licensed platform, or a bespoke build with ongoing support and regulatory updates.

Ask about CannaComply

How a build runs

  1. Week 1

    Scoping call and a one page requirement specification you sign off.

  2. Weeks 2 and 3

    Build, with a working version to review each week.

  3. Week 4

    Testing against the requirements, test evidence, user training and handover.

  4. After launch

    Change control for any updates, and a data export available at any time.

What you get with every build

  • User requirement specification
  • Role based access control
  • Audit trail on every record
  • Test evidence against each requirement
  • Change log
  • Data export in CSV
  • Hosting region agreed at scoping
  • You own the data and the code

Proof

Wilson Blaney, founder of Medicexum

Wilson Blaney

I have run quality for a FTSE 100 business, led a novel food dossier covering 860 products and sat through more inspections than I care to count. I build these tools because I have spent twenty five years watching good teams get caught out by bad spreadsheets.

About Wilson

Frequently asked questions

Bring the spreadsheet you trust least.

Tell us what it does and we will come back within one working day with a first view on scope and price.