ERP ADVISORY & SOFTWARE SELECTION FOR LIFE SCIENCES
Give your teams an ERP foundation that supports compliant scale without slowing science or tech transfer.
We help life sciences teams turn complex GxP requirements such as Part 11 e-signatures, audit trails, controlled documents, lot and expiry traceability, and Laboratory Information Management System (LIMS), Quality Management System (QMS), and Electronic Document Management System (EDMS) integrations into concrete ERP selection criteria, a weighted scorecard, and an implementation plan you can defend to QA, IT, and regulators.
How We Help Life Sciences Companies
We work across your software ecosystem including ERP, LIMS, QMS, Manufacturing Execution Software (MES), CRM, and outsourced partners to make sure the platform you pick can be validated and scaled from lab bench to commercial launch.
Turn regulations into concrete ERP requirements
We translate your GxP expectations into testable requirements: document lifecycles, independent audit trails, 21 CFR Part 11 e-signatures with manifestation on output, training gates, and role-based access. Those controls become RFP and demo criteria, not after-the-fact validation gaps.
Design ERP around lots, expiry, and QA release
We define how formulas, BOMs, bulk-to-fill and pack flows, quarantine, sampling, test results, COAs, and MRB decisions should behave in ERP. Vendors are asked to prove lot and serial genealogy, FEFO picking, and QC release gates using your scenarios, so traceability and recalls are managed in one system, not spreadsheets.
Connect CROs, CDMOs, and labs into a coherent picture
We map integrations to CROs, CMOs/CDMOs, CPOs, 3PLs, LIMS, and QMS so outsourced work still lands as clean, timely data inside ERP. For many clients, that includes CDMO-style project accounting (ASC 606), portals for sponsor visibility, and near real-time status across development and manufacturing.
Fold FDA Validation and other compliance controls into selection from day one
We build a GxP-aware scorecard, script demos with validation hooks, and score platforms not just on functionality but on “validate-ability” for IQ, OQ, and PQ. Then we stay in your corner through implementation and FDA validation, ensuring VMP, risk assessment, test scripts, and documentation are all aligned with the overall program, so the system passes audit and works in day-to-day use.
Why Life Sciences Companies Choose Us
OPERATIONS FIRST MINDSET
We speak lab, manufacturing sites and outsourced partners, not just platform
EXPANSIVE KNOWLEDGE
Knowledge of 40+ ERP vendors so you're matched with the right fit
EXPERIENCED LEADERSHIP
Engagement led by long-tenured leader from first conversation through go-live
ACTIONABLE, READY-TO-USE DELIVERABLES
Designed for your business but structured to plug into your project
Making Life Science Companies' Vision a Reality
The following are life science topic excerpts from our ERP Visions blog
