Pharma LIMS Software Built For GMP & Regulatory Audits
Pharmaceutical labs run under stricter scrutiny than almost any other industry — GMP, GLP, FDA 21 CFR Part 11 and NABL requirements all demand tamper-proof records, full traceability and instant audit readiness. Our pharma LIMS software (Pharmaceutical Laboratory Information Management System) is purpose-built for quality control labs, stability testing units and R&D departments that can't afford a failed audit or a lost batch record.
See A Live LIMS Demo First
Batch tracking, stability studies, electronic signatures aur audit trail — sab live demo mein dekho, 5 minute mein.
What A Pharmaceutical LIMS Needs To Handle
- Batch & sample testing — raw material, in-process and finished-product QC testing workflows
- Stability studies — scheduled pull dates, condition tracking, trend charts
- Electronic records & e-signatures — 21 CFR Part 11-style approvals with full audit trail
- Specification & OOS management — out-of-specification result flagging and investigation workflow
- Instrument integration — HPLC, GC and other lab instrument data capture
- Certificate of Analysis (CoA) generation — one-click, audit-ready PDF reports
- Change control & deviation tracking — documented, versioned, reviewable
- GMP / GLP / FDA compliance mapping — built around your SOPs, not a rigid template
Why Pharma Companies Choose Simpli Web
We already build compliance-first laboratory software for NABL-accredited labs, and the same audit-trail-first architecture carries over to pharmaceutical QC — full traceability from sample receipt to final certificate, reviewer/approver role separation, and reports formatted exactly the way inspectors expect to see them. See our broader LIMS software capabilities or the wider compliance software suite we build for NABL, NABH, BIS and QCI.
Frequently Asked Questions
Is your pharma LIMS software 21 CFR Part 11 compliant?
Yes. We build electronic records and electronic signature workflows that follow 21 CFR Part 11 principles — audit trails, restricted access, and reviewer/approver separation are built in, not bolted on later.
Can the LIMS handle stability study scheduling?
Yes — stability study modules track pull dates, storage conditions and result trends automatically, with alerts before a scheduled pull is due.
Does it integrate with lab instruments like HPLC?
Yes, our pharma LIMS supports instrument integration so results from HPLC, GC and similar equipment flow directly into the system instead of manual transcription.
How is pharma LIMS pricing decided?
Pricing depends on the number of users, instruments to integrate and the compliance scope (GMP, GLP, 21 CFR Part 11). Message us on WhatsApp with your lab's setup for a free quotation.