An intelligence hub innovating and accelerating groundbreaking therapies to address unmet medicinal needs
Please enter subscribe form shortcode
Please enter instagram feed shortcode
We scout for adjuvants globally from academia and industry (particularly the lesser known). We provide due diligence to understand the therapeutic potentials of your product. We establish strategies for quick advancement into acceptable medicinal product. We leverage appropriate advanced technologies to develop, redevelop or enhance product qualities.
We drive CMC, clinical proof of concept studies, and appropriate path to global markets.
We provide due diligence to Pharma/BioPharma/Cell-Gene Therapy companies to identify therapeutic gaps and opportunities. We identify your targeted medicines that could benefit from adjuvants for increased effectiveness. We provide appropriate adjuvants for combination therapies with your targeted medicines and drive advancement strategies.
We drive process and product improvements to increase specific activity of your single-target medicines for combinations with adjuvants.
From our experiences and numerous regulatory breakthroughs, we provide troubleshooting of your medicinal advancement challenges and provide creative strategies for quick resolution and regulatory approvals. Our scope includes functions of CMC (Process development, Analytical development, GMP Manufacturing, Quality assurance, Clinical development, and Regulatory) and involves quality investigations, operational leadership and creative strategies for rigor and speed.