Plans

Find out how SciNote can transform your lab.

Trusted by regulated R&D teams at BD, Qiagen, and the FDA.

Industry labs have stringent standards to uphold. SciNote’s industry plans are built around 21 CFR Part 11 and GxP compliance, audit trails and e-signatures, and validated installation with IQ/OQ documentation included from the start.

Why Industry Teams Choose SciNote

Compliance that’s already built in
SciNote meets 21 CFR Part 11, GxP, GLP, GMP, and ISO standards, with audit trails, electronic signatures, and role-based access controls in place from day one.

Validated deployment, documented from the start
So your team validates the system the same way it validates everything else that touches regulated data.

Built for client-facing, multi-site work
Organize by client, product, or project, and keep confidentiality intact across teams and locations — whether you’re a CRO managing five sponsors or a CDMO running parallel programs.

Audit-ready by default
Time-stamped, version-controlled documentation means an FDA or EMA inspection is something your team walks into prepared, not something it has to reconstruct the week before.

Built to scale with your business
As your programs grow, your protocols, methods, and institutional knowledge stay intact instead of resetting with every new client or product line.

Industry plans include onboarding built for unregulated as well as regulated environments, dedicated support, and validation-ready setup, along with the ongoing updates that keep your compliance posture current. See how SciNote holds up under your standards.

Book a demo with our team.

G2 reviews SciNote

“Main benefit and reason for having an electronic lab notebook is the creation of a searchable database, accompanied by significant time savings.”

jonas neuway

“Customer service was very prompt, courteous, knowledgeable… They provided background on the origins of the bug and laid out a timeline for resolving the issue.”

kyle envirlogix

“It allowed us to pick and choose which features of the software worked best for us and to define a company-wide method for recording data.”

Rita Cruz Ingenza