CDMO Services

End-to-End Solutions in Pharmaceutical Development

At Aurore Life Sciences, we provide GMP-compliant Contract Development and Manufacturing Organization (CDMO) services, offering dedicated solutions for the development and manufacturing of:

  • New Chemical Entities (NCEs)
  • Advanced Intermediates
  • High-Potency Drugs
  • Controlled Substances

With expertise in chemical synthesis and semi-synthesis, we ensure seamless support from early-stage R&D to full-scale commercial manufacturing, along with strong regulatory assistance. Our global presence and in-house capabilities allow us to manage the entire process with a single point of contact, ensuring complete accountability and efficiency.

Comprehensive

Project Management Approach

We understand the complexities of technology transfer and product development, which is why our dedicated project management team ensures smooth execution through:

Structured Planning & Tracking

A specialized team oversees timelines, resolves resource conflicts, and proactively addresses critical issues.

Seamless Communication

Regular updates, reports, and technical consultations (TCs) to keep customers informed at every stage.

Regulatory & Compliance Support

A highly experienced technical team collaborates directly with customers, providing insights to optimize the regulatory strategy

Our commitment to excellence and customer-centric approach make us a trusted partner among leading CDMO companies, delivering high-quality, innovative, and compliant solutions tailored to meet global pharmaceutical demands.