Pricing
Straightforward plans for labs of every size. All plans include a 7-day free trial.
Starter
For small teams getting started with digital lab management.
- Up to 3 team members
- Unlimited experiments
- Sample management
- Digital lab notebook
- Protocol library
- Audit trail (90 days)
- CSV / JSON export
- Email support
- Advanced analytics
- Approval workflows
- Multi-site management
- Priority support
Professional
For growing labs that need compliance, approvals, and deeper analytics.
- Up to 15 team members
- Unlimited experiments
- Sample management
- Digital lab notebook
- Protocol library
- Audit trail (unlimited)
- CSV / JSON export
- Email support
- Advanced analytics
- Approval workflows
- Multi-site management
- Priority support
Enterprise
For large institutions needing custom integrations, SLAs, and dedicated support.
- Unlimited team members
- Unlimited experiments
- Sample management
- Digital lab notebook
- Protocol library
- Audit trail (unlimited)
- CSV / JSON export
- Priority support
- Advanced analytics
- Approval workflows
- Multi-site management
- Dedicated onboarding & SLA
Save 20% with annual billing
Annual plans are available for all tiers. Contact us to switch.
Frequently asked questions
Is there a free trial?
Yes. Every new organisation gets a 7-day free trial with full access to all Professional features. No credit card required to start.
Can I change plans later?
Absolutely. You can upgrade or downgrade at any time. Changes take effect at the start of your next billing cycle.
What happens to my data if I cancel?
Your data is retained for 30 days after cancellation. You can export everything in JSON or CSV format at any time before or after cancellation.
Do you offer annual billing?
Yes. Annual billing is available at a 20% discount. Contact us to set up annual billing for your organisation.
Is Paraclyst suitable for FDA-regulated environments?
Paraclyst includes technical controls relevant to FDA 21 CFR Part 11 — including immutable audit trails, electronic signatures with password re-authentication, record locking, and protocol version archiving. Formal validation documentation (IQ/OQ/PQ) is the responsibility of the regulated organisation. Contact us for more information.