genae has extensive experience in a diverse number of therapeutic areas. Thorough understanding of the specific area of your therapy or device ensures compliance and facilitates in optimally executing your trial. Our unsurpassed network of Key Opinion Leaders enables finding the right sites at the right time.
You can count on genae for all phases of your clinical trial, from First In Human to observational registries. Since we are dedicated to medical devices only, we gained deep knowledge and understanding of device-based clinical research projects. We are aware that every project has different needs and regulatory requirements. Our team understands this and can help you with all different types of trials. We make sure your clinical trial will be optimally executed, so you can focus on your business.
Involving 1030 sites in 44 countries. Wherever you are, we can be too. genae offers global reach with offices in key research areas and involvement in more than 1030 sites.
450 active and completed medical device clinical trials. We are dedicated to medical device clinical trials and guide you through all stages.
More than 900 years of personnel experience in clinical research. genae was founded in 2005 and has quickly grown into a company with branches and key opinion leaders all over the world.
Involved in more than 120 Approval Studies. Do you need to obtain market approval? We make sure your clinical trial runs smoothly.
If you want to be sure about the outcome of your study, therapeutic insights of the CRO are indispensable. genae conducted hundreds of trials and therefore gained crucial therapeutic insights, from cardiovascular to neurological, that make a difference. Thanks to our expertise and know-how, you can rely on the outcome of your next study.
Conducting your trial in another country can be a challenge. Lack of knowledge can even slow down the process and make it more complex. genae has coverage across 6 continents and connections with key opinion leaders throughout the world. Our medical, operational and regulatory specialists have country-specific expertise. They understand the importance of local language, culture and processes. Thanks to this global expertise, we can proactively plan and execute trials of all sizes. We can help your trial advance faster and more efficient, in any country.
When you start your clinical trial, you want the outcome to be predictable. Of course, you also want your project to be executed on time and on budget. Throughout the development life cycle, genae provides medical and regulatory leadership and guidance, with efficient, disciplined operational execution of your studies around the world.
Want to hear more about our services or how we can support your clinical trial? Feel free to contact us with any questions you may have.Contact us