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SOLUTIONS

Pharma, healthcare and life sciences

Compliance, audit log and multi-site without SAP.

ISO and GMP audits, multi-site across plant, office and field, sensitive contracts that need qualified signing. Orquiva carries the legal weight without demanding 6 months of implementation or a €1,500/day consultant.

10 años

Legal retention period for payslips and contracts in Spain (Law 30/2015)

01 — THREE REAL INDUSTRY PAINS

And the three modules that fix them.

01

Immutable audit log, SIEM-exportable

Every action logged with SHA-256 timestamp. When the ISO 27001 audit lands, your CISO has the JSON ready in one click.

Audit & security →
02

Qualified eIDAS signing with no per-envelope fee

Confidentiality addenda, medical-rep contracts, GMP agreements. Qualified signing with full legal validity, no €4-per-document fee.

Signatures →
03

Documents with per-type GDPR retention

Full-text search inside PDFs. Each document tagged with its legal retention: payslip 10y, contract 10y, medical certificate per agreement.

Documents →

02 — FROM A REAL CUSTOMER

Founder Program · 2026 Pharma/Health Cohort

We reserve 3 founder-program spots for pharma, health and life-sciences companies. Priority access to audit log, org-wide MFA and GDPR retention configurable per data type.

03 — VS THE USUAL ALTERNATIVE

Why teams in this sector pick Orquiva

VS Legacy ERP (SAP SuccessFactors / Workday)

  • Implementation measured in weeks, not quarters — no mandatory consulting.

  • Transparent per-person monthly pricing, no perpetual licences or opaque renewals.

  • Modern product: your plant team uses it from mobile without 8 hours of training.

04 — IMPLEMENTATION

21

days

From signing to production.

Assisted migration from your current HRIS + per-site roles + audit with your DPO. 3 weeks from signing to production.

OTHER SECTORS

LET'S START

Want to talk about your team's case?