What We Deliver

PharmaActive is one of the MENA region’s leading pharmaceutical engineering partners — providing integrated solutions from feasibility study to compliant, operational facility. Founded in Jordan in 2017 and expanded into Saudi Arabia in alignment with KSA Vision 2030, we serve pharmaceutical, food, cosmetics, veterinary, and petrochemical industries with engineering depth, regulatory precision, and a 95% client return rate.
Our work spans three core pillars:

Machinery & Production Systems

Turnkey Engineering & Project Delivery

Accredited Calibration, Qualification & GMP Consulting

Pharmaceutical Production & Packaging Systems​

We integrate complete GMP-compliant machinery systems tailored to your production needs — from formulation through to final packaging.

Preparation & Formulation

Covers granulation (FBD and high shear), tablet compression and coating, capsule filling, liquid and semi-solid systems, and CIP/SIP integration.

Packaging Lines

Include blistering and cartoning, bottle filling and counting, powder filling, softgel encapsulation, and sachet and stick-pack systems.
All systems are designed for 21 CFR Part 11 compliance and scalable output, with more than 17 exclusive international agents supporting our product portfolio.

Serialization & Traceability

In collaboration with VISIOTT | TPS, we implement serialization and traceability as regulatory infrastructure — not a standalone add-on. Solutions cover serialization across ampoule, vial, bottle, and carton formats; aggregation systems; integrated weight control; tamper-evident labeling; and GAMP 5 and GMP-compliant architecture. Traceability is built into your production environment from the ground up.

Water & Utility Systems

In partnership with BRAM-COR, we engineer pharmaceutical-grade water and utility systems to pharmacopeial and GMP standards. This includes Purified Water (PW) and Water for Injection (WFI) systems, RO-EDI units, multi-effect distillers, pure steam generators, and storage and distribution loops.

Containment & Environmental Control

We supply and integrate isolators, LAF systems, misty showers, pass boxes, and cleanroom solutions — designed for controlled production environments and high-potency pharmaceutical applications.

Metal Detection & Product Integrity

Through CEIA, we implement high-sensitivity metal detection with auto rejection systems and 21 CFR Part 11 data logging — protecting product integrity and your brand at every stage of the line.

Turnkey Pharmaceutical Projects

PharmaActive delivers full lifecycle pharmaceutical facility projects, managing every phase from concept through operational handover. Our engineering and project management teams cover feasibility studies, conceptual and basic design, URS and P&ID development, detailed engineering, project management, construction supervision, commissioning and qualification, and training and handover.

We also apply Building Information Modelling (BIM) across new projects and facility expansions — reducing design clashes, improving coordination, and delivering time and cost savings before a single piece of equipment is installed.

GMP-by-design execution. From planning to operational readiness.

Accredited Calibration, Qualification & GMP Consulting

PharmaActive holds SAAC accreditation under ISO/IEC 17025:2017 — one of very few pharmaceutical engineering integrators in the region to offer accredited qualification services under the same structure as project delivery and machinery supply.

Our compliance services include:

Calibration Services

Covering mass and weighing instruments, environmental monitoring devices, pressure and differential pressure measurement, temperature and humidity measurement, volume instruments, analytical laboratory instruments, and calibration for utility and production equipment.

Cleanroom Qualification

Full qualification to GMP, ISO 14644, and FDA guidelines, including HEPA filter integrity testing (PAO), air balancing, ACH calculation, smoke testing, particle count, differential pressure, temperature and humidity, and utility performance testing.

Thermal Mapping

Conducted in accordance with GSP, GMP, GDP, FDA, and WHO guidelines, covering storage areas, cold storage equipment, transportation, and thermal processing equipment.

Systems & Equipment Qualification (IQ / OQ / PQ)

Comprehensive qualification for buildings, utilities, equipment, machines, and instruments.

GMP Consultation & Audit Readiness

Supporting businesses in optimizing operations, achieving required accreditations, and maintaining regulatory compliance.

Regional Presence

PharmaActive operates across Jordan, Saudi Arabia, Iraq, Egypt, Sudan, Oman, UAE, Palestine, Algeria, Lebanon, and broader MENA markets — bridging international technology with local regulatory frameworks and more than 53 client relationships across the region carton formats; aggregation systems; integrated weight control; tamper-evident labeling; and GAMP 5 and GMP-compliant architecture. Traceability is built into your production environment from the ground up.

Ready to Build or Upgrade?

Whether you’re upgrading a single production line or establishing a complete pharmaceutical facility, PharmaActive delivers engineered, compliant, and execution-ready solutions backed by accredited technical expertise and regional execution capability

Request a technical consultation to discuss your project.