Straight answers, from the engineers who do the work.

Pharmaceutical manufacturers and distributors, hospitals and clinical laboratories, food and beverage producers, mineral water plants, paint and chemical industry, warehouses and distribution networks, research institutes and educational institutions.

Our head office is in DHA Phase II, Islamabad, with a regional office in Lahore. Our engineers travel nationwide, and we have executed projects internationally including a QC laboratory in Liberia, West Africa.

Yes. QCS is ISO 9001:2015 certified (ISOQAR, UKAS accredited). We maintain PNAC traceability documentation, FBR legal registrations, master calibrator certificates and staff training records — all available in our company profile on request.

Yes. We use NIST-traceable standard materials and master calibrators. Our master calibrators are themselves calibrated by accredited calibration laboratories, which maintains an unbroken chain of traceability from your instrument to international standards.

Most calibrations are performed on site at your facility, which avoids transport risk and minimises downtime. Instruments that require laboratory conditions or repair are handled at our maintenance laboratory in Islamabad.

Typically annually, but the interval depends on the instrument's criticality, usage, manufacturer recommendation and your quality system. We help you set justified intervals and run a reminder schedule so nothing falls past its due date.

We record the as-found readings, notify you immediately and support an out-of-tolerance impact assessment on results produced since the last calibration. Where possible we adjust and re-calibrate; otherwise we quote repair or replacement.

Qualification (DQ, IQ, OQ, PQ) demonstrates that a piece of equipment is correctly specified, installed, operating and performing. Validation demonstrates that a process, cleaning procedure or analytical method consistently produces results meeting predetermined criteria. Equipment qualification is normally a prerequisite for process validation.

Either. We can author protocols and reports for your approval, or execute and document against protocols your quality unit has already approved.

A single instrument IQ/OQ/PQ is usually completed in one to three days on site. A full laboratory or facility program is scheduled by phase after a gap analysis, and typically runs over several weeks.

Thermal mapping documents and controls the temperature distribution inside a storage area, cold room, freezer or vehicle. It is required for organisations handling temperature-sensitive products — medicines, vaccines, biological products and foods — and identifies the hot and cold spots where permanent monitoring sensors must be placed.

A typical study runs a minimum of 24 to 72 hours per condition. Warehouses are usually mapped empty and loaded, and in both summer and winter conditions, to cover the worst case across the year.

Yes. We qualify refrigerated vehicles and distribution lanes as per WHO GDP guidelines, including door-opening and power-failure excursion studies.

Both. We deliver on-site trainings at your facility and in-house sessions at our premises, customised to your SOPs, equipment and audience.

ISO 9001, ISO 14001, ISO 45001, ISO 22000, ISO 13485, ISO/IEC 17025, HACCP and HALAL — through awareness and implementation training, documentation, internal audit and certification support with our partner bodies.

Yes. Every training closes with attendance records, competency assessment and certificates of participation suitable for your training files and audit evidence.

LABTRON is the QCS brand for laboratory equipment manufacturing, established in 2010. We manufacture under GMP conditions to USP and BP standards — stability chambers, column ovens, laminar flow hoods, dispensing and sampling booths, plus tablet testers including dissolution, disintegration, friability and hardness testers.

Yes. Every supply includes installation, commissioning, operator training, qualification documentation and ongoing backup support and maintenance.

Yes. Annual contracts bundle scheduled calibration, preventive maintenance and priority breakdown response at a fixed cost, which is how most of our long-standing pharmaceutical clients work with us.

We print pharmaceutical packaging materials: folding cartons, self-adhesive labels, blister and strip foils, patient information leaflets and package inserts, and corrugated shipper cartons. Every job runs against a controlled artwork master with a recorded version and an approved press proof.

Artwork is prepared or received, version-numbered and circulated for proof-reading. Nothing goes to press before your QA department signs the proof and shade card, and the released master is archived so any future reprint or regulatory query can be traced back to it.

The approved artwork master with version number, the signed press proof and shade card, a batch-wise print record, the delivery challan, and reconciliation of printed versus rejected material.

We are currently delivering three products — LIMS (Laboratory Information Management System), eBMR (electronic Batch Manufacturing Record) and HMS (Hospital Management System) — alongside corporate websites and portals. All are developed, hosted and supported by our own team.

Yes. Audit trails, role-based user access, electronic signatures and review workflows are built in, aligned to ALCOA+ data integrity principles and to 21 CFR Part 11 and EU GMP Annex 11 concepts, with development following GAMP 5.

Yes. Because the same team writes your validation protocols, every implementation ships with a computer system validation package — URS, functional and design specifications, executed IQ/OQ/PQ and a traceability matrix.

Yes. LIMS supports instrument connectivity and direct result capture from analytical instruments such as HPLC, GC and balances, which removes manual transcription and the data-integrity findings that come with it.