Diagnostics
Innovation
Biotech
Environment
Testing
Research
Diagnostics
Innovation
Biotech
Diagnostics
Innovation
Biotech
Environment
Testing
Research
Diagnostics
Innovation
Biotech
Ariba & Mac Limited is a Saudi joint venture between Ariba Health Care (USA) and Mac & Rains Group (Pakistan, UK, Turkey), bringing together 30+ years of global expertise in pharmaceuticals, biotechnology, and clinical research. We connect R&D organizations, clinical institutions, and pharmaceutical companies—delivering advanced research solutions, regulatory excellence, and technology-transfer services fully aligned with Saudi Vision 2030.
Ariba & Mac Limited provides integrated, research and innovation based services across Pharmaceuticals, Biotechnology, Healthcare, Cosmetology and Aesthetics by combining global expertise with local insight—ensuring compliance, innovation, and trust.
In the near future, Ariba & Mac Limited plans to establish a full-fledged International Research and Innovation Centre in Jeddah, Saudi Arabia, equipped with modern infrastructure for focused Cancer and Biotechnology Research, Development, and Technology Transfer. Our goal is to enable local commercial organizations to access high-quality R&D in the shortest possible time and at the lowest feasible cost, aligned with the broader objectives of Vision 2030.
We accelerate product development and access through R&D, regulatory strategy, CMC/manufacturing oversight, and market access—grounded in data and compliance.
Our lab delivers data-driven insights that help protect nature.
Formulation development, Analytical development, Validations for Pharmaceuticals, Biopharmaceuticals, Nutraceuticals & Cosmetics.
IND, IMPD, NDA, BLA, MAA, Medical devices, eCTD and DMF; FDA/EMA/SFDA/MENA/MHRA/GCC/DRAP.
CMO/CDMO/CRO selection & oversight, process design and scale-up to GMP commercial.
Value communication, payer strategy, launch planning and execution.
We combine FDA/EMA/SFDA/MHRA/GCC/DRAP know-how with on-the-ground partners to de-risk timelines and ensure compliant delivery—from technology transfer to launch.
End-to-end guidance across IND, IMPD, NDA, BLA, MAA, Medical devices, eCTD and DMF.
From CMO/CDMO/CRO selection to GMP launch with measurable milestones.
We've compiled answers to the most common questions about our lab services, research process, and capabilities.
We provide formulation, validation, analytical & microbiology testing, CTD/DMF support and technology transfer services.
Yes. We scope custom R&D programs with defined deliverables, timelines and regulatory pathways.
Timelines depend on dosage form and regulatory needs. We provide a project plan with milestones after the initial consultation.
We work with certified partners and maintain cGMP-ready documentation and validation practices.
Use the contact form to outline your needs. We will schedule an advisory call and share a document checklist.