As a FULL SERVICE CRO we meet all your needs in the area of clinical investigation and other related fields
European regulatory consultation, and management of clinical trials and investigational projects with medicinal products and medical devices.
Focused on start-up: Essential documentation, approval from authorities, ECs, autonomous communities, AEMPS, EMA, management and negotiation of contracts as well as management of amendments.
The experts at Alpha Bioresearch assume the management and monitoring of your project, providing personnel specialized in on-site, telephone and online monitoring.
Our tools allow us to work with the highest quality and safety standards, complying with European regulations.
With more than 20 years of experience, Alpha Bioresearch has the necessary personnel and knowledge to be able to offer the highest satisfaction guarantee.
The consultancy offers you the opportunity and flexibility to adjust your work force according to the necessities and size of your project, providing specialized personnel.