Precision Weighing for Pharmaceutical & Life Sciences
GMP-compliant instruments · ISO/IEC 17025 calibration · DAC/ENAS traceable · JAFZA support
Pharmaceutical manufacturing in the UAE operates under some of the strictest measurement requirements in any industry. From raw material dispensing to finished-product checkweighing, every weighing step must satisfy ICH Q7, GMP Annex 15, and UAE Ministry of Health audit trails. AND Gulf has supplied GMP-grade A&D Japan balances and calibration services to pharmaceutical facilities across the GCC for over 40 years, with factory-level diagnostics and same-day calibration certificates available from our JAFZA base.
Analytical balances used in pharmaceutical dispensing must deliver repeatability within ±0.1 mg and maintain linearity across the full capacity range. A&D Japan's Super Hybrid Sensor (SHS) technology combines electromagnetic force restoration with single-point parallelogram load sensing, achieving 1-second stabilisation without sacrificing accuracy at the extremes of capacity. The BM Series micro-analytical balances extend this to 0.001 mg readability for API formulation work, while the GH and GR Series cover the 120 g–310 g range required for most solid-dosage dispensing.
Moisture content is a critical quality attribute for active pharmaceutical ingredients, excipients, and finished tablets. The A&D MS-70 and MX-50 moisture analyzers use Secondary Radiation Assist (SRA) halogen heating — a technology that provides uniform heat distribution without hotspots — to deliver repeatable loss-on-drying results in under 5 minutes. Resolution to 0.001% moisture content satisfies pharmacopoeial drying specifications including USP ⟨731⟩ and BP moisture methods.
AND Gulf's calibration service issues certificates that document the full measurement uncertainty budget to k=2 (95% confidence) with DAC/ENAS traceable reference weights. These certificates are formatted for direct submission to GMP auditors and the UAE Ministry of Health. Our mobile calibration lab can perform on-site work at your facility across Dubai, Abu Dhabi, and the wider GCC — eliminating the instrument downtime and chain-of-custody risk of sending balances off-site.
Key Requirements in This Sector
- ICH Q7 / GMP Annex 15 audit trail for all weighing operations
- Readability to 0.1 mg (analytical) or 0.001 mg (semi-micro / micro)
- ISO/IEC 17025-traceable calibration certificates
- Stable performance under HVAC air currents in clean rooms
- USP ⟨731⟩ / BP-compatible moisture determination
- Same-day calibration service for production continuity
Recommended Instruments
BM Series — Micro Analytical Balances
0.001 mg readability with built-in ioniser for static-free API dispensing
GH Series — Semi-Micro Analytical Balances
Motor-driven internal calibration, 120 g capacity, GMP-grade draft shield
GR Series — Analytical Balances
Fully automatic self-calibration, 30% smaller footprint than conventional balances
MS-70 / MX-50 Moisture Analyzers
SRA halogen heating, 0.001% resolution, USP/BP moisture method compatibility
Calibration Services
DAC/ENAS traceable certificates, GMP audit-ready format, on-site UAE/GCC
Frequently Asked Questions
What balance readability is required for pharmaceutical dispensing in UAE?
How often must pharmaceutical balances be calibrated in the UAE?
Are AND Gulf calibration certificates accepted by UAE GMP auditors?
Equip your pharmaceutical facility with GMP-grade instruments
Speak to our team about balances, moisture analyzers, and calibration packages for your UAE or GCC site.
AND Gulf FZE · Jebel Ali Free Zone (JAFZA), Dubai · +971 4 881 9900