GMP line and batch checks
Record line clearance, in-process checks, yield and reconciliation checks and batch documentation with user and time stamps.
Industrial pharma
QHSE software for compliant pharmaceutical manufacturing
Run GMP line checks, cleanroom and utility inspections, deviation follow-up and CAPA in one system. Give production, quality and EHS teams the same evidence, from the warehouse to the packing line.
Built for regulated production
Quality and safety checks that stand up to inspection
Configured for the pace of a production suite, a warehouse or a utilities plant, with controlled evidence at every step.
Cleanroom and utility inspections
Check cleanliness, differential pressure, temperature, humidity, HVAC, water and compressed-air systems on a fixed schedule.
Equipment and calibration readiness
Inspect production equipment, balances, sensors and emergency systems, and escalate overdue calibration or maintenance.
Deviations, CAPA and change control
Capture deviations, investigate root causes and track corrective actions through to effectiveness checks.
Supplier and incoming material checks
Approve suppliers, inspect deliveries and track certificates, non-conformances and corrective actions.
Controlled documents and training
Give teams the current SOP, batch record or work instruction, with revision history and read-and-understood evidence.
From line finding to verified close-out
Product quality depends on the follow-through
A line clearance check finds a damaged sieve and a temperature excursion on a critical utility. Both are recorded with a photo and routed to production and engineering before the next batch starts.
The fixes are uploaded, the line is re-checked and the batch record is closed. The quality team can show the finding, owner, action and verification in one place at the next GMP inspection.
- Findings assigned with owner and due date
- Photo evidence before and after the fix
- Audit history by line, site and standard
The quality loop
Plan, check, correct, prove
A consistent audit rhythm that connects frontline checks to GMP, ISO and customer evidence.
01
Plan
Schedule GMP checks, cleanroom rounds and equipment inspections by line, standard and risk.
02
Check
Teams complete mobile checks with scores, photos and notes.
03
Correct
Assign findings, escalate overdue actions and verify the fix.
04
Prove
Export GMP, ISO and customer-audit evidence by site or production line.
FAQ
Industrial pharma: frequently asked questions
Can we score audits and track trends?
Yes. Checks can use weighted scoring, so you can compare lines, sites and audit cycles and focus on repeat findings.
Does it support GMP and ISO 9001?
Yes. The system supports controlled documents, GMP line checks, deviations, CAPA, change control, internal audits and management review evidence.
Can staff use it on shared devices?
Yes. Role-based access and QR codes let staff open the right checklist quickly while keeping permissions and records attributed.
Can we link incidents and CAPA?
Yes. Incidents, audit findings and deviations can create corrective actions with an owner, due date and verification step.
Can we use it alongside our electronic batch record?
Yes. InspecOps complements the batch record by capturing the checks, evidence and actions around each batch, with exports that fit your quality system.
How long does rollout take?
A production line or warehouse is typically live in days. Multi-site rollouts with templates, permissions and training usually take a few weeks.
Keep exploring
See Industrial pharma inspections in action
Bring a real site, checklist or high-risk activity. We will map it to InspecOps and show you the evidence trail it creates.