Research & Development

Our Research & Development division is the scientific backbone of Ariba & Mac Limited. We deliver research-driven solutions across Pharmaceuticals, Biotechnology, Cosmetics and Nutraceuticals — turning evidence into compliant, market-ready products in the shortest possible lead time.

In most cases, having an R&D facility is very expensive and tiring, requiring a lot of expertise. Sometimes, both the development costs and the time invested exceeds initial estimates. Therefore, outsourcing product development is the most recommended track.

From concept to commercialization, our scope covers formulation design, patent drafting, CTD/DMF preparation, validation & qualification, and complete documentation. We integrate modern analytical methods and experienced scientific oversight to meet global regulatory expectations.

Comprehensive R&D Capabilities

Our dedicated research team of experienced scientists and inventors, is committed to developing a range of formulations and products as per customer specifications and regulatory requirements.

• Generic & Novel Formulation Development for Regulated and Semi-regulated Markets.
• Preparation and Filing of Patents, CTDs and DMFs for Global Submissions.
• Method/Process Development, Validation, Qualification, Trouble Shooting and Document Develpement.
• Clinical Research & Trials Support
• Batch Records, Stability Programs, and Quality Documentation.
• Technology Transfer and Scale-up with CMOs/CDMOs/CROs.
• Training Programs for Scientific & Clinical Professionals.
• Research Collaborations with Universities & Institutes

Formulation & Development

Design and optimize dosage forms to ensure efficacy, safety and stability using robust pre-formulation and analytical data.

Validation & Documentation

Comprehensive validation protocols and traceable documentation enabling GMP readiness and regulatory inspections.

Testing & Quality Control

Analytical, Microbiological and Stability Testing to ensure product quality throughout development.

Our Approach

We align R&D with regulatory and commercial objectives from day one, integrating quality-by-design and risk-based thinking.

• Cross-functional collaboration between research, regulatory and quality teams.
• Compliance mapped to SFDA, FDA, EMA, MHRA, GHC, MENA and DRAP frameworks with data integrity.

Initial Consultation

Define scope, dosage forms, timelines and regulatory pathways; align on data and deliverables.

Laboratory Testing

Execute analytical and microbiological methods, stability studies and iterative optimization to meet specifications.

Research Collaborations & Partnerships

We connect universities, CMOs/CDMOs/CROs and manufacturing partners to accelerate innovation and ensure successful technology transfer.

Technology Transfer

Seamless transition from pilot to commercial scale with complete methods, materials and process documentation.

Global Compliance Support

Support for eCTD/DMF preparation for IND, IMPD, BLA, MAA and NDA filings with SFDA, FDA, EMA, MHRA, MENA and GHC coordination.

Innovation & Knowledge Sharing

Joint Research, Training and Skill Development Programs for Scientists, Clinicians and Young Professionals.