Ariba & Mac Limited (KSA) bridges the gap between Research & Development Organizations, Clinical Research Institutions and Pharmaceutical Companies, with Technology Transfer facilitation, regulatory expertise, facility setup, and research based services for investors, with a vision to integrate science, innovation, and patient care.
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.
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.
Ariba & Mac Limited is a Saudi Arabia–based joint venture between Ariba Health Care Limited (USA) and Mac & Rains Group (Pakistan, UK, and Türkiye). Together, we deliver integrated solutions in Pharmaceuticals, Biotechnology, Healthcare, Cosmetology, Aesthetics, Research Innovation and Technology Transfer , combining global standards with regional insight to drive sustainable progress.
With its valuable assets like 500+ expert scientists and inventors, trained staff, and sophisticated infrastructure, Ariba & Mac Limited encourages collaborations with international companies. These activities help us track our developmental activities against the highest benchmarks.
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We support pharmaceutical companies, healthcare investors, beauty & wellness brands, and clinical institutions with strategic, scientific, and regulatory expertise — delivering compliant, market-ready outcomes.
Drug discovery, analytical testing, formulation, and biotech innovation programs.
Trial design, CRO management, site coordination, and GCP compliance.
Process optimization, validation, scale-up, and GMP manufacturing support.
eCTD submissions, SFDA/FDA/EMA compliance, and post-market support.
Audit readiness, QMS design, validation, CAPA, and compliance audits.
End-to-end project setup for pharma, hospitals, and aesthetics ventures.
Clinical dermatology, hair restoration, lasers, and nutraceutical innovations.
Injectables, PRP, regenerative treatments, and anti-aging innovations.
Turnkey development of healthcare facilities with planning, equipment, compliance, and quality.
Evidence‑based assessments covering Science, Operations, Regulatory Posture, and Market Outlook.
Our tailored training programmes upskill your entire workforce with courses taught by instructors
Scholarship and training programs to support student, young professional and early career researchers.
From GMP plant design to Aesthetics programs and Clinical research, we combine scientific rigor with practical execution to deliver compliant, market-ready outcomes.
Proven Track Record
End‑to‑end support across consultancy, clinics, and labs—seamless from strategy to delivery.
Global Regulatory Mastery
Expertise with FDA, EMA, SFDA, MHRA, GHC,MENA, DRAP—built‑in compliance and faster approvals.
We partner with Pharmaceutical & Biotech companies, Hospitals & Clinics, Dermatology/Aesthetic centers, Nutraceutical & Skincare brands, Universities and Research Institutes. We also serve Investors/Startups, Venture Capitals and Bank due diligence, across KSA, MENA, USA, UK and Europe.
Strategic Consultancy, Facilities and Research Services for Regulated Markets.
Master planning, facility setup, Equipment selection, Validation support, QMS & SOP, commissioning and staff training, Product development & Stability, Bioequivalence and Regulatory support.
Clinic/Hospital planning, Diagnostic lab setup, Equipment selection, Validation support, QMS & SOP, commissioning and staff training.
Evidence-driven Cosmetology and Aesthetic programs including lasers & injectables. We serve for Clinic design, Laser and Devices selections, SOP trainings and medical-grade skincare protocols.
Academic-commercial collaborations, and startup advisory.
Our process is built on clarity, accuracy, and scientific rigor. From the moment a sample/research project arrives at our Research Center, it goes through a series of carefully managed steps — including analysis, validation, and expert review.
You'll meet with our scientific advisors to define your research goals, scope, timeline, and budget.
Our team selects the right techniques, tools, and protocols to meet your scientific and regulatory requirements.
Using advanced equipment and strict quality controls, we carry out all procedures with precision to develop your product.
Instead of rigid pricing, Ariba & Mac offers adaptable collaboration models designed to fit the scope, scale, and complexity of your project. We believe in aligning with your goals, not forcing one-size-fits-all solutions.
Ideal for defined deliverables and specific timelines.
For ongoing advisory and continuous support.
Strategic partnerships for long-term growth and innovation.
Find quick answers about our consultancy scope, facility setup support, regulatory pathways, and laboratory services.
We provide end-to-end consultancy in pharmaceuticals, healthcare facilities, cosmetology, aesthetics, and research laboratories. Our expertise includes facility setup, regulatory compliance, technology transfer, and scientific advisory.
Yes. We specialize in regulatory pathways for FDA, EMA, SFDA, MHRA, MENA, GHC, DRAP, and other global authorities. Our team guides clients from dossier preparation to final approval, ensuring compliance with international standards.
Absolutely. Our R&D and technology transfer services are tailored to client needs. We collaborate on product development, stability studies, bioequivalence, and process optimization to move innovations from lab to market.
Yes. Our network of laboratories operates under international quality standards including GLP, GMP, and ISO accreditations. This ensures reliable, reproducible, and compliant testing for our partners.
You can start by reaching out through our contact form or scheduling a consultation. Our team will review your requirements and propose a tailored engagement model that fits your project scope and objectives.
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