Formulation & Development

End-to-end formulation solutions designed to accelerate your molecule from early feasibility to commercial readiness. We integrate QbD-driven methodologies, analytical science, and regulatory alignment to deliver stable, scalable, and high-performance formulations for global markets.

Supporting innovators, generic pharma, and biotech companies worldwide.

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Accelerating Your Molecule From Concept to Clinic

Our formulation development approach ensures that scientific risk is minimized early, performance is optimized using structured experimentation, and every stage is supported by robust analytical insights. With deep experience in multiple dosage forms and complex molecules, we shorten development cycles and deliver formulations that are ready for scale-up and regulatory submission.

Formulation Services We Offer

Our laboratories are equipped with cutting-edge analytical platforms, formulation suites, and controlled facilities that support complete end-to-end development workflows.

Pre-Formulation Studies

Solubility, pKa, excipient compatibility, polymorph screening, and risk assessment to determine the most robust formulation strategy.

Prototype Development

Rapid development of multiple prototype formulations across diverse dosage forms using QbD-driven experimentation.

Scale-Up & Tech Transfer

Transition of optimized formulation into pilot and commercial batches with complete documentation and support for receiving sites.

Stability Studies

ICH-compliant accelerated and long-term stability studies with integrated analytical support and real-time evaluation.

Bioavailability Enhancement

Specialized solutions including solid dispersions, lipid-based systems, nanosuspensions, and solubilization strategies.

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Regulatory Support for Formulation

CMC documentation, pharmaceutical development reports, and formulation-specific responses to regulatory queries.

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Dosage Forms We Support

Across small molecules & complex formulations.

Pre-Formulation Assessment

Understanding physicochemical properties and identifying critical formulation risks.

Prototype Design

Developing initial formulations aligned with the target product profile and performance requirements...

Optimization & Robustness

Refinement using DoE and QbD tools to enhance stability, manufacturability, and bioavailability.

Scale-Up & Tech Transfer

Supporting process optimization, equipment selection, and pilot-scale manufacturing.

Stability Studies

Accelerated and long-term ICH studies to confirm product stability and shelf-life.

Regulatory Documentation

Preparing complete pharmaceutical development reports and CMC sections for global submissions.

Integrated Analytical Science

Analytical development is tightly integrated with formulation activities to provide faster decision-making and complete product characterization. Our analytical team ensures each formulation stage is supported with high-precision data, validated methods, and compliance with the latest ICH and GMP requirements.

Need formulation development support?

Share your molecule details and project requirements our formulation scientists typically respond within 24–48 hours with next steps and feasibility evaluation.