Spain is one of the most attractive countries in the world to carry out clinical trials, especially in the area of oncology.
The high quality of the Spanish health system, the scientific level of researchers, the great recruiting potential of Spanish hospitals, and the competitive local costs position Spain as a preferred destination for biotech companies developing anti-cancer drugs.
Below we provide a list of 11 clinical research organizations (CROs) capable of managing and monitoring oncology clinical trials in Spanish hospitals:
Sofpromed is a full-service Clinical Research Organization (CRO) specialized in the management of phase I-IV clinical trials worldwide for biotechnology and pharmaceutical companies across all therapeutic areas. Being a cancer-focused CRO since its beginnings, Sofpromed has particularly strong capabilities to run oncology trials in Spain.
As a Contract Research Organization (CRO) Leon Research offers solutions that include all the activities related to the design, start-up, and follow-up of clinical trials and research studies in Spain. Leon Research manages the whole process to introduce a new medical device or drug into the market, from medical writing to data management and registration.
Effice has been offering quality clinical research services in Spain for more than 19 years, as a Contract Research Organization (CRO) with highly qualified personnel. Effice is specialized in providing full clinical research services to both pharmaceutical and biotechnology companies, as well as independent researchers who wish to conduct high-quality clinical studies within available resources.
Along the last 25 years, Sermes CRO has evolved from being a traditional company to a new technology driven CRO. From the very protocol conception, we deliver tailor-made solutions that will help you through the whole drug development cycle. Clients can rely on Sermes’ strategic scientific, clinical, and regulatory advice, supported by a strong business know-how.
BioClever is a provider of outsourced development and commercialization services to pharmaceutical, biotechnology, medical device and health organizations. We focus our efforts on the factors that are critical to our clients (reducing times, reducing cost, and increasing quality). Our team of experts has extensive experience in a broad range of therapeutic areas.
Apices was born in 2009, founded by a group of highly qualified professionals with a vast experience in CROs and pharmaceutical companies. We are an organization with Spanish identity and international vocation. We add value to customer in study design, clinical development planning and successful regulatory timelines to achieve customers milestones.
Anagram was founded in 1998. We are a Clinical Research Organization (CRO) with integrated Imaging Core Lab based in Spain which provides high quality services in clinical development and post-authorization trials with drugs and medical devices. We partner with our clients by getting proactively involved in each stage of the project, from study design to final deliverable.
Evidenze is a full service CRO with experience in all research stages, from clinical trials (Phases 1-4) to observational and real-world evidence (RWE) studies. We work in all research phases. We are partners of the biomedical sector, with an internal multidisciplinary structure that can meet the most demanding needs, creating differential and value solutions thanks to the synergism of knowledge between our units.
Pivotal provides full Contract Research Organization (CRO) services and builds a flexible client relationship by offering a variety of contracting models, from single source to full service. From protocol conception to publications, Pivotal’s scientific team provide tailored risk-management strategies to optimize our clients’ products chances of making it to the market.
ClinicalTrialsTeam was founded in 2016 by professionals with more than 20 years of hands-on clinical trial experience. We are a globally focused company whose main goals are to offer the highest quality and to satisfy clients demands without forgetting industry requirements and regulatory compliance. Based in Madrid (Spain), our highly qualified professionals are trained and ready to develop projects within the European Union (EU) and abroad.
QualitecFarma® is a Contract Research Organization (CRO) with headquarters in Madrid and offices in the US. We provide value-adding consultancy and support services to the biopharmaceutical industry. Our area of work is focused on clinical trials, clinical and post-marketing pharmacovigilance, regulatory affairs, strategic development, and search for business opportunities for our clients.
