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Industry /003/ of 11

Phar­ma­ceu­ti­cals

AI That Helps Pharma Teams Move Faster. Research assistants, document intelligence, and validated automation for compliant lab work.

designed around
GxP21 CFR Part 11GDPRHIPAAICH E6

Outcomes

What changes
for your team

The stuff pharmaceuticals teams tell us they want more (or less) of.

  1. /001/

    Research teams move from literature search to synthesis in hours, not weeks

  2. /002/

    Regulatory submissions assembled with traceable evidence and version control

  3. /003/

    Lab data captured cleanly and aligned with study protocols

  4. /004/

    Pharmacovigilance signals reviewed faster, with audit-ready records

What we build

What we build
for pharmaceuticals

Starting points, not a menu. We pick the one that fits your workflow and make it work properly.

/001/

Research copilots

Search across internal studies, patents, and public literature with cited answers.

/002/

Regulatory assistants

Draft and check submission documents against the latest FDA/EMA guidance.

/003/

Trial data automation

Structured capture from CRFs, sites, and lab feeds with validation built in.

Standards

Rules we
design around

Compliance isn't a checkbox at the end. We build with these in mind from the first sprint.

/001/GxP
/002/21 CFR Part 11
/003/GDPR
/004/HIPAA
/005/ICH E6

Your move

See it on
your data

A short discovery call covers your workflow, the constraints and an honest read on fit. No deck, no boilerplate.