Transforming Molecules Into Market-Ready Products

We provide integrated pharmaceutical research services — from formulation development and analytical method design to scale-up, stability studies, and regulatory documentation. Accelerate your molecule with science-driven development, global-quality systems, and faster turnarounds.

Your Partner for End-to-End Pharmaceutical Development

From feasibility and prototype design to stability and regulatory readiness, we support R&D teams with deep expertise across formulation science, analytical development, and quality compliance. Our QbD-driven workflows, advanced technologies, and multidisciplinary scientific team ensure faster problem-solving, higher success rates, and smoother transitions to commercial scale.

Our Core Services

We provide integrated pharmaceutical research services — from formulation development and analytical method design to scale-up, stability studies, and regulatory documentation. Accelerate your molecule with science-driven development, global-quality systems, and faster turnarounds.

Formulation & Development

Designing stable, scalable, and bioavailable formulations across dosage forms using QbD-based strategies.

Analytical Development

Method development, validation, stability-indicating methods, impurity profiling, and release testing.

Stability Studies

ICH-compliant accelerated and long-term stability programs with real-time analytical evaluation.

Scale-Up & Tech Transfer

Seamless transition of optimized formulations to pilot and commercial facilities.

Bioavailability Enhancement

Specialized solutions: solid dispersions, lipid systems, nanosuspensions, and solubilization techniques.

Regulatory Support

CMC documentation, development reports, validation summaries, and global submission readiness.

Advanced Capabilities & Technologies

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

10+ HPLC Systems

Precision chromatography platforms for complex methods

Pilot-Scale Formulation Facility

Structure confirmation & impurity identification

Pilot-Scale Formulation Facility

Granulation, compression, coating, encapsulation

ICH-Compliant Stability Center

25°C/60%RH, 30°C/65%RH, 40°C/75%RH, photostability

Why Pharmaceutical Teams Choose Us

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

QbD-Driven Scientific Approach

Risk-based formulation and analytical development to ensure robustness and consistency.

Integrated Development Model

Formulation + analytical teams work together for faster decisions and fewer iterations.

Regulatory-Aligned Documentation

ICH, GMP, FDA & EMA-ready reports, methods, and audit-friendly data integrity practices.

Faster Development Timelines

Rapid prototype cycles, predictive analytical insights, and efficient project management.

Transparent Communication

Clear documentation, weekly updates, and complete visibility at every stage.

Certified Excellence. Global Trust.

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