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Team of experienced professionals having over 20 year's experience, We can help clients shape their product offerings by continually innovating and developing new technologies and processes. So it’s fair to say, we know what we’re doing. We are ideally placed to deliver a wide range of GMP-compliant services from our dedicated development facilities, each designed to adapt to customer needs.



Analytical research and development (AR&D) offers standalone services and supports our formulation development activities. The AR&D teams are integrated with preformulation, product development and quality assurance teams to ensure effective and accelerated product development. Our experience in developing methods for highly complex and unstable drug products.

Global out-license collaborations of development assets

Out licensing

Cuckos is working to expand its global strategic marketing partnerships for products developed-in house. Cuckos products typically incorporate proprietary platform technology offering a therapeutic benefit and generic complex products. Cuckos aims to provide patent protection for its products and we work closely with our partners to ensure that an effective life-cycle management strategy is in place.


Identifying and collaboration with right manufacturing sites which suits your product, Cuckos has the capabilities to deliver your project from development through to the manufacture of large commercial batch sizes of tablets, capsules or powders.

Regulatory Affairs

Cuckos helps pharmaceutical companies to manage their regulatory affairs portfolio by way of Regulatory Strategies, Feasibility Studies, Dossier compilation and filings, Agency follow ups & approvals, Post Approval License Management, Regulatory Compliance, Gap Analysis and Regulatory due diligence

Need A Development CRO

Developing pharmaceuticals can be a tricky business, so let us help.

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