Crafting Precision
Redefining Discovery

Welcome to Aurore Life Science’s Analytical Research and Development (R&D) hub, where scientific curiosity meets precision instrumentation. At the forefront of innovation, we harness cutting-edge equipment and advanced techniques to unravel the complexities of API characterization. We strategically aim to optimize processes, streamline workflows, and reduce costs while maintaining the highest quality standards.

  • Precision in Equipment

    Our Analytical R&D division boasts an arsenal of high-end equipment, meticulously curated to meet the demands of modern pharmaceutical analysis. From state-of-the-art spectroscopy tools to ultra-high-performance liquid chromatography (UHPLC) systems, each instrument is a beacon of accuracy, enabling us to decipher the intricate molecular landscapes of APIs.

  • Unraveling Complexity

    Characterizing complex APIs demands ingenuity. Armed with advanced techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, and X-ray crystallography, we navigate the intricate structures of pharmaceutical compounds. This ensures a comprehensive understanding of APIs' physicochemical properties, enabling us to shape formulations with precision.

  • Optimization and Cost-Efficiency

    In our pursuit of excellence, we believe that optimization should complement innovation. Aurore's Analytical R&D is dedicated to minimizing costs without compromising quality. By employing robust Design of Experiments (DoE) methodologies and process analytical technologies (PAT), we enhance efficiency, reduce wastage, and deliver value that resonates across the entire pharmaceutical journey.

Our Comprehensive

Range of Services

Method Development and Validation

Crafting robust analytical methods tailored to your specific APIs, ensuring accurate characterization and reliable results.

Analytical Support for Formulation Development

Collaborating with formulation teams to optimize drug delivery systems by understanding the interaction between APIs and excipients.

API Characterization

Employing advanced spectroscopic, chromatographic, and mass spectrometric techniques to unravel the molecular makeup and physicochemical attributes of APIs.

Process Optimization

Enhancing manufacturing efficiency by developing in-process control strategies using process analytical technologies (PAT) and Design of Experiments (DoE) methodologies.

Structural Elucidation

Utilizing cutting-edge tools like NMR spectroscopy and X-ray crystallography to decipher complex molecular structures, aiding in precise formulation design.

Regulatory Support

Providing analytical data packages for regulatory submissions, ensuring alignment with global quality and safety standards.

Impurity Profiling

Thoroughly identifying and quantifying impurities, including degradation products and process-related impurities, to ensure safety and compliance.

Method Transfer and Training

Facilitating smooth method transfer between laboratories and providing training on advanced analytical techniques.

Stability Studies

Conducting rigorous stability assessments to determine API shelf-life and storage conditions, facilitating formulation stability and regulatory compliance.

Consultation and Collaboration

Offering expert consultation and collaboration on analytical challenges, aiding in problem-solving and innovative solutions.