Become a partner. Help regulated companies get audit-ready.

Join our partner network helping pharma, medical device, and financial services companies deploy compliance systems - audit-ready in weeks, not months.

The partner opportunity

What your clients are dealing with:

audit deadlines approaching with no system in place - SOPs in shared drives, approvals over email, training tracked in spreadsheets
enterprise QMS platforms that cost $200K+/year, take 6-12 months to implement, and require dedicated admin teams
growing out of spreadsheet-based quality systems but not ready for enterprise overhead

How we engage together:

guided setup ($15-30K) delivers an audit-ready compliance system in weeks
all modules included - document control, CAPA, training, change control, audit management
self-hosted deployment option for data sovereignty requirements

Referral partners

Earn recurring revenue by connecting regulated companies with a compliance system that actually deploys. We handle the implementation - you make the introduction.

What referral partners do:

identify companies preparing for audits - ISO 13485, FDA inspections, SOX compliance reviews - without adequate systems
make warm introductions between quality/compliance leaders and our team
position the guided setup as a low-risk path to audit readiness

Good fit for:

quality consultants advising life sciences companies
regulatory affairs advisors in pharma, med devices, or banking
technology advisors working with regulated mid-market companies

Solution partners

Build a practice around compliance system deployments. Learn our two-layer methodology, earn from implementation services, and resell licenses at competitive margins.

What solution partners do:

map quality processes using the Business layer - document types, approval chains, training requirements, regulatory scope
configure and deploy compliance modules on the Automation layer - document control, CAPA, training, change control, audit management
lead guided setups to get clients audit-ready in weeks
extend the platform for client-specific workflows - cross-site tracking, ERP integrations, custom approval chains
resell Comind.work licenses directly to clients

Good fit for:

GxP validation and compliance consulting firms
system integrators serving regulated industries
IT consulting firms with pharma, med device, or financial services clients

Industries we serve together

Pharma & biotech

QMS for FDA 21 CFR Part 11, ICH Q10, GAMP 5. Document control, CAPA, deviation management, batch release workflows.

Medical devices

QMS for ISO 13485, EU MDR, MDSAP. Design controls, DHF management, post-market surveillance, risk management.

Banking & financial services

Compliance management for SOX, Basel III, OSFI. Approval workflows, policy management, audit trails, regulatory reporting.

Become a partner

Tell us about your business and which partnership type interests you most.