Full Service CRO for Oncology Trials in Europe

CRO for cancer clinical trials. Regulatory, monitoring, data management, and pharmacovigilance services for the pharma and biotech industries.

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The Oncology CRO

Regulatory and monitoring services for phase I-IV clinical trials in cancer

Regulatory Monitoring

Full Service CRO for Clinical Trials in Spain

by Patricio Ledesma | 9 March, 2019 | CRO Spain | 0 Comments

Sofpromed is a full service contract research organization (CRO) specialized in the management of phase I-IV clinical trials in Spain. In this article we describe how we help pharma, biotechnology, and academic research sponsors to conduct their clinical trials in...

10 Things You Should Know About Rare Cancers and Clinical Trials

by Patricio Ledesma | 1 March, 2019 | Rare Cancers | 0 Comments

Rare cancers represent nearly 20% of all cancer cases. Many of them do not have effective treatments. Are there clinical trials for rare tumors? If you are looking for comprehensive and reliable information about rare cancers, and particularly on clinical trials...

Is Your Clinical Trial Ready for an Audit?

by María José López | 27 February, 2019 | Quality | 0 Comments

According to ICH-GCP, section 5.19.1: “The purpose of an audit, which is independent of and separate from routine monitoring and quality control functions, should be to evaluate trial conduct and compliance with the protocol, Standard Operating Procedures (SOP), Good...

OUR FOCUS: WE MANAGE CANCER TRIALS IN EUROPE

Sofpromed is a European full service contract research organization (CRO) specialized in the integral management of phase I-IV clinical trials and observational studies in oncology. We manage both adult and pediatric clinical studies in Europe, with wide expertise and knowledge in solid tumors (soft-tissue sarcomas, bone tumors, gastrointestinal, endometrial, ovarian, and breast cancer), hematologic malignancies (leukemia and lymphomas), and rare cancers.