Pre-formulation & Feasibility Studies

We conduct comprehensive pre-formulation studies to evaluate the physicochemical properties of drug substances and identify potential development challenges. These studies support informed decision-making and establish a strong foundation for successful formulation development.

Oral Solid Dosage Forms (Tablets & Capsules)

Our team develops robust and scalable oral solid dosage formulations, including immediate-release, modified-release, and combination products. We focus on achieving optimal product performance, manufacturability, and patient compliance.

Liquid, Topical & Injectable Formulations

We provide formulation development support for oral liquids, suspensions, creams, gels, ointments, and sterile injectable products. Our approach ensures product stability, efficacy, and compliance with regulatory requirements.

Formulation Optimization & Troubleshooting

We help resolve formulation and manufacturing challenges through systematic investigation and scientific problem-solving. Our experts optimize product performance, improve stability, and enhance manufacturing efficiency.

Stability Studies & Product Characterization

We design and manage stability studies to evaluate product quality throughout its shelf life. Our characterization services provide critical insights into product attributes, supporting development, regulatory submissions, and lifecycle management.

Technology Transfer & Scale-Up Support

We facilitate the successful transfer of formulations and processes from laboratory development to pilot and commercial manufacturing. Our scale-up strategies help ensure process consistency, product quality, and operational efficiency.

Regulatory & CMC Documentation Support

We prepare high-quality scientific and technical documentation to support regulatory submissions and compliance activities. Our expertise includes formulation development reports, CMC documentation, CTD Module 3 support, and technical dossier preparation.