Sign Up
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.
Access the signup page
Section titled “Access the signup page”- Navigate to
/signupin your browser. - Alternatively, on the login page, select the Create workspace link.
Step 1: Account details
Section titled “Step 1: Account details”Create your personal account by providing the following:
- Enter your Full Name.
- Enter your Email address. This will be your login identifier and used for verification codes.
- Select Next to proceed to workspace setup.
Step 2: Workspace setup
Section titled “Step 2: Workspace setup”- Enter a Workspace Name (typically your organization or facility name).
- Select your Industry from the dropdown:
- Medical Devices
- Pharmaceuticals
- Biotechnology
- Life Sciences
- Food & Beverage
- Cosmetics
- General
- Select Next.
Step 3: Compliance standards
Section titled “Step 3: Compliance standards”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).
- Review the pre-selected ISO Standards checkboxes:
- ISO 9001, ISO 13485, ISO 14001, ISO 45001, ISO 27001, ISO 17025
- 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
- Toggle any checkboxes on or off to match your organization’s requirements.
- Select Next.
Step 4: AI workflow preview
Section titled “Step 4: AI workflow preview”The system generates a tailored workspace configuration based on your industry and compliance selections. This step presents three interactive, collapsible sections for your review.
Suggested workflow
Section titled “Suggested workflow”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).
Document templates
Section titled “Document templates”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.)
Compliance summary
Section titled “Compliance summary”A consolidated view of your selected ISO standards and GMP compliances, along with your industry badge and recommendation source (AI Engine or Industry Config).
- Review all three sections. Expand or collapse each section by selecting its header.
- Select Confirm & Continue to proceed.
Step 5: Instant workspace setup
Section titled “Step 5: Instant workspace setup”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.
Modules
Section titled “Modules”All 13 modules are enabled by default. Toggle any non-essential module off if your organization does not need it:
| Module | Description |
|---|---|
| Document Control | Document lifecycle, versioning, approval workflows (required) |
| Training | Training assignments, quizzes, competency tracking |
| CAPA | Corrective & preventive actions with effectiveness reviews |
| Deviations | Non-conformance reporting and investigation |
| Audit Management | Internal/external audits, findings, action tracking |
| Change Control | Controlled change requests with impact assessments |
| Equipment & Calibration | Asset registry, calibration schedules, maintenance |
| Suppliers & SCARs | Supplier qualification, risk classification, corrective actions |
| Complaints | Customer complaint intake, investigation, resolution |
| E-Signatures | 21 CFR Part 11 compliant electronic signatures |
| AI Analytics | AI-powered dashboards, severity classification, RCA |
Default groups
Section titled “Default groups”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.
Default job roles
Section titled “Default job roles”Pre-populated job roles based on your industry (e.g. QA Manager, Quality Engineer, Regulatory Specialist). Remove any roles that do not apply.
Step 6: Select a plan
Section titled “Step 6: Select a plan”Choose the plan that fits your organization. All plans include access to all enabled modules with full enterprise-grade features.
| Feature | Starter | Professional |
|---|---|---|
| Users | Up to 5 | Up to 25 |
| Modules | All 13 | All 13 |
| AI features | Included | Included |
| E-signatures | 21 CFR Part 11 | 21 CFR Part 11 |
| Validation package | Self-generating | Self-generating |
| Support | Standard | Priority |
| 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.
- Select your plan (Starter or Professional).
- Select Subscribe & Create Workspace to proceed to Stripe Checkout.
Already have an account?
Section titled “Already have an account?”If you already have an account, select Login at the bottom of the signup page to return to the login page.