The QMS team is largely responsible for document preparation, control and distribution, ensuring all WHO, MOH, UAE, EMEA and US FDA guidelines are strictly adhered to. They also take on the management of all internal audits, annual training plans, medical checkups, signature controls and certification for ISO 9001:2015.


The GMP compliance team are responsible for compliance at all ADCAN facilities. They have control over batch release, deviation, change control, CAPA, complaints, recalls, quality risk management and the return of goods. ADCAN also has a well-established IPQA laboratory for in-process controls.

Quality Control Lab

ADCAN’s Quality Control Laboratory is one of the most well-equipped in the world, with the most advanced technical instruments put to use in carrying out all necessary testing relating to the physical, chemical and micro aspects of our products.

Regulatory & Pharmacovigilance

Our Regulatory Department is well-established and is responsible for developing fully-compliant product dossiers according to ICH guidelines. ADCAN is fully committed to responding effectively to any adverse event reporting relating to our products, from the market, hospitals or any other establishment, as set out in guidelines from the UAE’s Ministry of Health

Feedback can be submitted by a doctor or pharmacist. Simply contact pv@adcanuae.com.


ADCAN’s engineering and maintenance teams work according to Good Engineering Practices, and all our utilities have been installed with the support of leading partners. All our utilities are monitored through our Building Monitoring System (BMS), with real time data recorded to ensure they meet GMP requirements.