Redefining functional pharmaceutical outsourcing through a global network of biotech experts and consultants.
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.
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
Our Biotech Experts help you navigate the continuously evolving regulatory environment while focusing on your business goals.
Our integrated cross-functional team of experts, and customized biologics solutions move your projects forward efficiently and effectively.
We closely monitor preclinical studies and ensure that instructions procedures are followed, data generated are reliable and GLP compliant.
We provide scientific support on all aspects of your program, Iincluding pharmacology, (bio)analytical methods, immunology or data analysis.
We established a network of qualified suppliers that cover you from late discovery through to clinical study needs – a fit for purpose vendor selection.
We established a broad network of qualified regulatory, toxicology, CMC, and clinical consultants to complement your team in a cost-efficient way.
Our wealth of experience and knowledge allows us to advise on the design of toxicology studies and handle unforeseen events during your program.
Once your clinical strategy is set, we help you select and manage your CRO with the appropriate expertise.
We help you navigate the biologic product development process to overcome regulatory challenges and complexities unseen in traditional development.
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.
Vaccine development has a unique regulatory approval process that focuses on stimulating the immune system. Let our team guide you through the process.
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.
