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New users can create an account and set up a workspace through the guided signup wizard. The wizard walks you through six steps to configure your quality management environment and select a plan.

What takes others 6+ months and multiple consultants, InnoQualis does instantly. No setup fees. No implementation costs. No consultants required. Your fully configured, compliance-ready workspace is ready in minutes — not months.

  1. Navigate to /signup in your browser.
  2. Alternatively, on the login page, select the Create workspace link.

Create your personal account by providing the following:

  1. Enter your Full Name.
  2. Enter your Email address. This will be your login identifier and used for verification codes.
  3. Select Next to proceed to workspace setup.
  1. Enter a Workspace Name (typically your organization or facility name).
  2. Select your Industry from the dropdown:
    • Medical Devices
    • Pharmaceuticals
    • Biotechnology
    • Life Sciences
    • Food & Beverage
    • Cosmetics
    • General
  3. Select Next.

Based on your industry selection, the system provides recommended ISO standards and GMP compliances. Recommendations may come from an AI engine or from built-in industry configurations (indicated by a badge).

  1. Review the pre-selected ISO Standards checkboxes:
    • ISO 9001, ISO 13485, ISO 14001, ISO 45001, ISO 27001, ISO 17025
  2. Review the pre-selected GMP Compliances checkboxes:
    • 21 CFR Part 820, 21 CFR Part 11, EU GMP Annex 11, EU GMP Annex 15, ICH Q7, PIC/S GMP
  3. Toggle any checkboxes on or off to match your organization’s requirements.
  4. Select Next.

The system generates a tailored workspace configuration based on your industry and compliance selections. This step presents three interactive, collapsible sections for your review.

A visual pipeline of the recommended document lifecycle for your industry. For example, a Medical Devices workspace sees:

Draft → Peer Review → QA Review → Approve → Effective → Periodic Review

The workflow name and steps vary by industry (e.g. Pharma GxP Workflow, Food Safety QMS Workflow).

A grid of recommended document types for your industry, each showing:

  • Template name (e.g. SOP, Design Control, Batch Record)
  • Description of its purpose
  • Category badge (Core, Engineering, Compliance, Quality, etc.)

A consolidated view of your selected ISO standards and GMP compliances, along with your industry badge and recommendation source (AI Engine or Industry Config).

  1. Review all three sections. Expand or collapse each section by selecting its header.
  2. Select Confirm & Continue to proceed.

This is where InnoQualis eliminates the setup burden that other QMS platforms impose. While traditional QMS implementations require months of consulting, manual configuration, and costly onboarding, InnoQualis auto-configures everything based on your industry selection. You review, adjust if needed, and you are ready to go.

All 13 modules are enabled by default. Toggle any non-essential module off if your organization does not need it:

ModuleDescription
Document ControlDocument lifecycle, versioning, approval workflows (required)
TrainingTraining assignments, quizzes, competency tracking
CAPACorrective & preventive actions with effectiveness reviews
DeviationsNon-conformance reporting and investigation
Audit ManagementInternal/external audits, findings, action tracking
Change ControlControlled change requests with impact assessments
Equipment & CalibrationAsset registry, calibration schedules, maintenance
Suppliers & SCARsSupplier qualification, risk classification, corrective actions
ComplaintsCustomer complaint intake, investigation, resolution
E-Signatures21 CFR Part 11 compliant electronic signatures
AI AnalyticsAI-powered dashboards, severity classification, RCA

Pre-populated organizational groups based on your industry (e.g. QA Team, Engineering, Manufacturing, Management). Remove any groups that do not apply to your organization.

Pre-populated job roles based on your industry (e.g. QA Manager, Quality Engineer, Regulatory Specialist). Remove any roles that do not apply.

Choose the plan that fits your organization. All plans include access to all enabled modules with full enterprise-grade features.

FeatureStarterProfessional
UsersUp to 5Up to 25
ModulesAll 13All 13
AI featuresIncludedIncluded
E-signatures21 CFR Part 1121 CFR Part 11
Validation packageSelf-generatingSelf-generating
SupportStandardPriority
Price£12,000/month£24,000/month

Plans are billed annually. There are no setup fees, no implementation costs, and no consultant requirements. You get a production-ready QMS from the moment your workspace is created.

  1. Select your plan (Starter or Professional).
  2. Select Subscribe & Create Workspace to proceed to Stripe Checkout.

If you already have an account, select Login at the bottom of the signup page to return to the login page.