cro.lifespex.de
Your trusted CRO partner
LX CRO helps manufacturers in the life sciences sector access the European market and maintain a sustainable market presence. As a full-service contract research organisation (CRO), we specialise in clinical investigations and clinical evaluations.
Full-Service CRO
Solutions for every stage of your product lifecycle
Our services are designed both for established manufacturers of medical devices and IVDs as well as small start-ups preparing for market entry. The MDR (Medical Device Regulation, Regulation (EU) 2017/745) and the IVDR (In Vitro Diagnostic Medical Devices Regulation, Regulation (EU) 2017/746) impose stringent requirements on the development and commercialisation of medical devices and IVDs.
We advise you with these regulatory requirements and support you throughout every stage of your product lifecycle.
Why LX CRO?
Because experience and efficiency make the difference
The regulatory requirements for medical devices and IVDs are extensive and complex. With LX CRO at your side, you have a partner who will guide you safely and efficiently through every stage of your clinical investigation.
Our experts in medicine, life sciences and engineering can offer decades of experience in planning, conducting and documenting clinical evaluations and clinical investigations.
Excellence
Our in-depth expertise and continuous improvement from project to project ensure the highest quality at every stage.
Experience
Our multidisciplinary team of scientists, engineers and physicians combines decades of experience in clinical studies and regulatory processes.
Reliability
Clear communication, transparent processes and consistent on-time delivery enable reliable planning.
Flexibility
We provide solutions tailored your specific needs—for start-ups, SMEs and global enterprises.
Partnership
Successful collaboration is built on reliability and commitment. We work alongside you towards shared goals.
Effiziency
We reduce complexity, translate your needs into clear requirements and develop practical solutions that save time and resources.
Clinical Product Lifecycle
Your partner at every stage
As your CRO, we support you throughout the product lifecycle—from development and market launch to post-market surveillance.
Our structured approach ensures efficient delivery. We assess your needs, design fit-for-purpose clinical investigations and conduct them to the highest standards. Moreover, we support you towards conformity assessment and post-market surveillance activities.
You can benefit from our experience.
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Packages
From initial guidance to full-service delivery
Make the most of our multidisciplinary team.
As a full-service life sciences CRO, we are your qualified partner for small work packages as well as complete studies—from the initial project concept and clinical data collection to the final clinical report and beyond.
A Clear Strategy Starts Here
Get in touch to discuss our packages and services.
Whether you need an initial assessment or detailed information, we will connect you with the right experts.