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The Strategic Biotech Consultants for Outsourcing Drug Development to World Class CROs

Redefining functional pharmaceutical outsourcing through a global network of biotech experts and consultants.

About Us

Your One-Stop Drug Development Partner

KreaMedica is your general contractor in the biotech industry. With complete transparency, we help you identify suitable vendors, prepare and manage budgets, oversee and monitor day-to-day activities, and hand you the keys upon program completion (submission).

KreaConnect provides a tool to quickly identify and engage the right consultants/experts to plan your programs. With our broad network of experts, we have expertise in regulatory, CMC, pharmacology, toxicology, and clinical areas.

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Our Services

Combining Capital with Collaborative Drug Development Consultants.

KreaMedica is a collaborative drug development company that works with international biotech and pharma clients. We plan, manage, and execute programs from lead candidate selection through non-clinical safety assessments, and early clinical trials. Our rapid and streamlined contracting process provides our clients with a “one-stop-shop” experience for outsourcing to a world-class CRO/CMO network

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Regulatory Strategy

Our Biotech Experts help you navigate the continuously evolving regulatory environment while focusing on your business goals.

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Monitoring & Auditing

We closely monitor preclinical studies and ensure that instructions procedures are followed, data generated are reliable and GLP compliant.

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Vendor Selection

We established a network of qualified suppliers that cover you from late discovery through to clinical study needs – a fit for purpose vendor selection.

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Project Management

Our integrated cross-functional team of experts, and customized biologics solutions move your projects forward efficiently and effectively.

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Scientific Support

We provide scientific support on all aspects of your program, Iincluding pharmacology, (bio)analytical methods, immunology or data analysis.

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We established a broad network of qualified regulatory, toxicology, CMC, and clinical consultants to complement your team in a cost-efficient way.

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Our Expertise

A Few Areas Of Our Core Expertise

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General Toxicology

Our wealth of experience and knowledge allows us to advise on the design of toxicology studies and handle unforeseen events during your program.

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Once your clinical strategy is set, we help you select and manage your CRO with the appropriate expertise.

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We help you navigate the biologic product development process to overcome regulatory challenges and complexities unseen in traditional development.

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Delivery of medicines to the lung is an elegant way to target the respiratory tract – but also challenging. However, with our help, you can easily navigate the obstacles.

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Vaccine Development

Vaccine development has a unique regulatory approval process that focuses on stimulating the immune system. Let our team guide you through the process.

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Central Nervous System

Medications acting on the CNS have complex pharmacology, must often cross the blood-brain barrier and bear potential abuse liabilities. Let our CNS experts assist you.

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Truth in Numbers


Development Programs


Sponsors Who Trust Us


Years Combined
Industry Experience


Don’t take our word for it.

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