Expertise in developing parenteral dosage forms distinguishes Quraxia within the industry. Leveraging advanced pharmaceutical science and technologies, the team navigates the unique challenges of injectable drug formulation with strategic insight and innovative problem-solving.
Core capabilities include:
Process development for solubilizing poorly water-soluble drugs, stabilizing sensitive molecules, and selecting optimal excipients for compatibility and efficacy.
Sterility assurance and aseptic manufacturing, utilizing the latest sterilization methods and contamination control protocols.
Analytical rigor guided by Quality by Design (QbD), ensuring consistency, purity, and safety through all stages from pre-formulation to scale-up.
Full regulatory support with thorough validation and documentation for compliance across global frameworks.
Stability and packaging solutions designed to safeguard product integrity throughout shelf life and distribution.
This comprehensive approach anticipates challenges, delivers creative solutions, and facilitates seamless technology transfer to commercial manufacturing.
