

Mid-Market Manufacturing ERP Software Selection Guide 2026
How should a mid‑market manufacturer actually choose ERP? This 2026 field guide starts on the plant floor, turning routings, WIP, quality, and costing into clear selection criteria. Then it shows how to run scripted demos with your own jobs and items, use objective fit‑gap scoring, and avoid pitfalls like bad labor reporting, UoM conversions, and fragile scheduling. The goal is simple – pick a manufacturing ERP system that holds up under real load.

John Hannan
9 min read


Understanding ERP Selection Roles: Perspective, Expertise, and Where Bias Can Influence Decisions
ERP can deliver meaningful business value, but the path to getting there is often more complex than leadership expects. One reason is that ERP decisions involve multiple participants with different expertise, responsibilities, and perspectives.

John Hannan
4 min read


ERP selection and validation in FDA‑regulated companies (CSV & 21 CFR Part 11)
Most teams treat validation after vendor choice—backwards. This guide shows how to bake CSV and 21 CFR Part 11 into ERP selection: translate URS into measurable criteria, compare vendors on audit trails, e‑signatures, and role security, and outline a pragmatic VMP with risk‑based IQ/OQ/PQ. The goal is selection that stands up in audit and in operations—no bolt‑on validation scramble later.

John Hannan
6 min read


A Practical ERP Software Selection Playbook for Confident, Defensible Decisions
Software selection becomes risky when decisions hinge on demos instead of evidence. This guide shows how to structure selection with clear criteria, weighted scorecards, scripted day-in-the-life demos, integration and data checks, and TCO analysis. Built from 25+ years of running selections across manufacturing, distribution, and life sciences, it’s a vendor-neutral playbook for confident and defensible decisions that hold up on go-live day.

John Hannan
7 min read


FDA ERP Validation Checklist & Templates for 21 CFR Part 11
Learn how to validate an ERP system for FDA 21 CFR Part 11 and GxP without bloating scope. This guide shows a risk‑based path through IQ/OQ/PQ, the exact Part 11 controls to prove (e‑signatures, audit trails, timeouts, lockouts), and the evidence auditors expect for backup and restore. Includes concise test snippets you can copy and a downloadable checklist, risk traceability matrix, and test‑case template to accelerate your project. Useful for NetSuite, SAP, and D365 in regu

John Hannan
5 min read


Considerations for Your Business When Selecting a New ERP System
Most organizations expect an ERP system to support the business for seven to ten years or longer, which makes the selection process a strategic decision rather than a simple software purchase.

John Hannan
9 min read


ERP Stakeholders and Their Role in Software Selection and Implementation
ERP touches the core of the business. When stakeholder input is too narrow, companies often select systems based on polished demonstrations, executive preference, vendor familiarity, or incomplete requirements.
John Hannan
9 min read


Understanding 21 CFR Part 11 Compliance when selecting a new ERP System
21 CFR Part 11 must provide complete documentation of process controls, record and data integrity safeguards, accuracy assurances, and user authentication and authorization processes.
John Hannan
4 min read


ERP Guidance to Help Life Sciences Companies Reduce Recall Risk and Improve Product Quality
Recall readiness is not a single feature. It is the ability to detect an issue, contain it quickly, and prove what happened with an audit ready trail.
John Hannan
3 min read


7 Steps To Choosing the Right ERP Software
These steps are designed to help leadership teams evaluate options objectively, involve the right stakeholders, compare vendors consistently, and select a solution that supports both where the business is today and the capabilities needed to support future growth.
John Hannan
6 min read






