Where We Excel

We excel in manufacturing sterile and complex drug products, meeting stringent GMP requirements with dedicated capabilities for aseptic processes and complex dosage forms.

Whether it’s high potency APIs or challenging formulations, we pride ourselves on our flexibility and innovation, tailoring solutions that others may find daunting. Our facilities include ISO 5 suites for aseptic processing, lyophilization capabilities for biologics, and specialized technologies like nanomilling under aseptic conditions.

At Agno Pharma, we prioritize quality and precision in all stages of development. Our analytical services are conducted under full cGMPs, offering robust method development and validation tailored to each phase of your project. As a client-focused CDMO, we ensure a smooth transition from clinical trials to commercial manufacturing, supported by ICH-compliant stability programs and a state-of-the-art electronic lab management system for enhanced data integrity and reporting.

Partner with us to navigate the complexities of drug development and accelerate your path to market success.