Speeding up clinical trial initiation Speeding up clinical trial initiation timelines is a very critical factor for study sponsors. Therefore, the faster a clinical study is initiated, the better....
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How are clinical trials conducted? What is a CRO? Read our articles and learn more about clinical trials and contract research organizations.
How to Carry Out a Cancer Clinical Trial in Spain?
Cancer clinical trials are complex and sponsors should know in advance the critical aspects and local procedures that will be needed to undertake such large and demanding venture. This knowledge...
Why Should Pharma and Biotech Consider Spain for their Cancer Clinical Trials?
Spain is a great country to conduct clinical trials. By the end of 2018, according to ClinicalTrials.gov, the American database of clinical studies carried out worldwide, Spain is the fifth European...
Which Electronic Data Capture System Should I Use?
There are several types of electronic data capture (EDC) solutions that can be used to manage data in clinical trials. The selection of the data management tool will depend on the size of the study...
What is an eCRF?
An eCRF (electronic case report form) is a software system used to collect data in a clinical study. Commonly, eCRFs are web-based applications containing various data forms and fields designed to...
Reducing Data Queries Through Optimized eCRF Design
Cleaning data in clinical trials can be a tedious task when the electronic case report form (eCRF) has not been properly designed. Identifying and resolving discrepancies in data is a...
How to Conduct High Quality Clinical Trials
The term "quality", when talking about clinical trials, is related to various elements and concepts. But what are the basics of quality that any clinical trial should meet? On what grounds is...
Sofpromed Extends Clinical Operations in Europe
Sofpromed, a full service contract research organization (CRO) focused on cancer trial management, has announced the extension of its clinical operations to provide local service in additional...
Clinical Trial Regulatory Affairs in Spain
Clinical trials involve several regulatory affairs before, during, and after the research. In Spain, trial sponsors need to interact with the ethics committee (EC) and the competent authority (CA),...
CRO for Clinical Trials in Spain
Sofpromed is a full-service contract research organization (CRO) headquartered in Spain. Thanks to its location, Sofpromed can provide local clinical trial management services in Spanish cities, for...
International Multicenter Clinical Trials: Benefits and Challenges
International multisite trials are complex and costly. Large numbers of hospitals and patients cause practical challenges.