CLAUSE Ltd is a Contract Research Organization (CRO).
We provide clinical trial organizing services all over Europe to Pharmaceutical and Medical devices companies All our team consists of experienced CRAs and Project Managers who have been working since 2005 in various therapeutic fields, such as cardiology, dermatology, gastroenterology, orthopedics, endocrinology, pulmonology, pediatrics, otolaryngology, nephrology and other.
Medical Device Trial
Full range of clinical trial services for Medical Device companies.
Regulatory Support
Regulatory approval is the first step to organize you clinical trial.
Feasibility Services
Can Feasibility data be reliable?
Pharmacovigilance
We guarantee the result, we guarantee the terms.
Certification of Medical Device
Get a CE-certificate for your medical device. Which country better to choose? Click here to learn more.
Registration of Medical Device
From establishment registration and listing to 510(k) - we manage all the process of registration establishment and products on the US market.
Laboratory Logistic and Managment
Laboratory management and logistics. Step by step.
Project Management
Getting the Project Management right is the key to achieving a successful result at each stage of clinical trial organizing.
Auditing Service
Clause offers a full range of auditing services.
Trainings
We offer interesting workshops and various training programs in the field of clinical research.
Clinical monitoring
With Clause your clinical trial is under the strict monitoring
Why CLAUSE?
- Providing high quality services
- Low cost services
- Flexibility
- Excellent Communication