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.

 

The Oncology CRO

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

RegulatoryMonitoring

Full Service CRO for Clinical Trials in Spain

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

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?

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.

SERVICES

Regulatory Affairs

Ethics Committees Competent Authority Insurance policies

Site Selection & Activation

Selection visits
Site contracts
Initiation visits

Recruitment Support

Communication with sites
Randomization
Progress reports

Monitoring

Onsite visits
Source data verification
CRF review

Data Management

eCRF/DB design
Data cleaning
Query resolution

Logistics Management

Biological sample shipments
Drug distribution
Trial materials

Pharmacovigilance

SAE/SUSAR management
EudraVigilance
Safety reports

Biostatistics

Sample size
Statistical programming
Statistical analysis

Medical Writing & Translations

Protocols
Informed consents
Publications

Project Management

Planning & follow-up
Quality control
Financial management

CUSTOMERS

Pharmaceutical & Biotech Companies

 

Research Groups

 

Hospitals & Institutes

 

Independent Investigators

 

ARE YOU PLANNING A CLINICAL TRIAL IN SPAIN?

We help sponsors from the US, EU, & Asia to recruit fast in Spanish hospitals

Our Oncology Expertise

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