Intermediary services for Biopharma, Biotech & Cosmestics companies.
We act as intermediary and support Contract Research organizations to deliver succesful preclinical studies
OUR MISSION IS TO EMPOWER YOUR SUCCES THROUGH PRECLINICAL STUDIES
Are you facing challenges to perform pharmacology, toxicity or efficacy studies for your products due to Limited Resources, Lack of Expertise, Time Constraint, Limited Infrastructure, Regulatory Compliance?
Our team of experts, with over 25 years of experience, is dedicated to ensuring that your preclinical studies are efficient, cost-effective, and successful.
Choosing the right CRO for your research project can be a daunting task
Partnering with us maximizes your potential for success.
We streamline your search for the most suitable CRO, SAVING valuable time and resources. We ensure that the chosen CRO possesses the necessary expertise and capabilities to meet your specific requirements. By harnessing the expertise of top-notch CROs, we enable you to achieve successful outcomes in your research and development endeavors.
ABOUT PROMAFUN CRIO
> Meet Our Dedicated Team
Meet the team of project managers, scientists, study managers and operations experts, all driven by a common goal: to empower your success through preclinical studies.
> Current Vacancies
HOW DO WE OPERATE?
We collaborate within a vast network of leading CROs, research centers and advisors in immunology, vaccinology, virology, cancer, and drug discovery offering access to world-class scientific expertise and state-of-the-art technologies.
Why PROMAFUN CRIO?
- ☑ Cost-effective services
- ☑ Quality according to GLP guidelines 100% 100%
- ☑ Experts/Advisors with 25+ years of experience
- ☑ Customer Service and Customer Relationships 100% 100%
We offer a range of Services
By assessing feasibility at the outset, project managers and researchers can anticipate any potential problems and make sure that everything is in place for a successful study outcome.
Preclinical studies are essential in the drug development process to ensure that the drug candidates are safe and effective before entering clinical trials.
Site Study Auditing
- We audit test sites to confirm studies were performed according to GLP guidelines.
- We provide training and GLP advice.
- We review documentations required to start the study.
Pharmacology & Toxicology Studies
Animal models permit researchers to assess the potential toxic effects of a drug candidate on living organisms. These toxicity studies help determine the maximum safe dose and the potential causes of adverse effects.
Data Management & Biostatistics
Data management is crucial for results coming from preclinical studies. It assist with improved decision-making, improve data quality, reduce costs, comply with regulations and improve performance.
Efficacy studies for cancer, bacterial and virus infections: vaccines, drug compounds, and antibodies
Determining the drug candidate’s efficacy – An animal model can help determine the effectiveness of the drug candidate in treating or preventing a specific disease or condition