Bioclever
BioClever is a Contract Research Organization (CRO) based in Spain, specializing in clinical trials, observational studies, and related services. They focus on providing high-quality, customized solutions for pharmaceutical and medical device development, ensuring compliance with international standards and regulations. Their mission is to support the development of new drugs and treatments through expert management, innovative technology, and a commitment to quality and integrity.
Industries
Nr. of Employees
medium (51-250)
Services
Protocol development and start-up activities for a range of trial designs including randomized, blinded, crossover and placebo-controlled studies.
End-to-end project management for clinical studies, including risk management, milestone tracking and client liaison.
Monitoring services delivered by CRAs to ensure site compliance, recruitment performance and data quality through study conduct to close-out.
CRF/eCRF design, database build and validation, coding of adverse events, data processing and maintenance of data traceability.
Statistical design, SAP development, sample size calculations, randomization, interim analyses, adaptive designs, DSMB support and production of statistical reports and TLFs.
Mapping and conversion of clinical study data to SDTM/ADaM, generation of define.xml, XPT files and supporting documentation for regulatory submissions.
Protocol development and start-up activities for a range of trial designs including randomized, blinded, crossover and placebo-controlled studies.
End-to-end project management for clinical studies, including risk management, milestone tracking and client liaison.
Monitoring services delivered by CRAs to ensure site compliance, recruitment performance and data quality through study conduct to close-out.
CRF/eCRF design, database build and validation, coding of adverse events, data processing and maintenance of data traceability.
Statistical design, SAP development, sample size calculations, randomization, interim analyses, adaptive designs, DSMB support and production of statistical reports and TLFs.
Mapping and conversion of clinical study data to SDTM/ADaM, generation of define.xml, XPT files and supporting documentation for regulatory submissions.
Expertise Areas
- Clinical trial management
- Clinical monitoring and CRA services
- Data management and electronic data capture (EDC)
- Biostatistics and statistical programming
Key Technologies
- Electronic data capture (eCRF/EDC)
- Interactive Web Response System (IWRS)/RTSM
- Electronic Trial Master File (eTMF) and CTMS
- ePRO and patient data capture systems
News & Updates
BioClever joins REVASCAT ischemic stroke trial
BioClever participated in the REVASCAT trial, which revealed benefits of a new treatment for ischemic stroke, including data management and statistics.
BioClever organizes coaching event with European University of Madrid
BioClever hosted a coaching event on leadership and management, emphasizing professional development.
BioClever and UFV organized conference on 21st-century vaccines
The event included expert speakers discussing vaccines' importance and impact, with participation from industry professionals.
BioClever's participation in clinical trials in Barcelona and Madrid
BioClever conducts clinical trials in Barcelona and Madrid, offering services from trial design to monitoring and data analysis.
The key role of Contract Research Organizations
An overview of CROs' importance in clinical research, highlighting BioClever's role in Spain.
eCRFs: Ensuring quality for your clinical trial results
The significance of electronic case report forms in clinical trials for data accuracy and efficiency.
BioClever joins REVASCAT ischemic stroke trial
BioClever participated in the REVASCAT trial, which revealed benefits of a new treatment for ischemic stroke, including data management and statistics.
BioClever organizes coaching event with European University of Madrid
BioClever hosted a coaching event on leadership and management, emphasizing professional development.
BioClever and UFV organized conference on 21st-century vaccines
The event included expert speakers discussing vaccines' importance and impact, with participation from industry professionals.
BioClever's participation in clinical trials in Barcelona and Madrid
BioClever conducts clinical trials in Barcelona and Madrid, offering services from trial design to monitoring and data analysis.
The key role of Contract Research Organizations
An overview of CROs' importance in clinical research, highlighting BioClever's role in Spain.
eCRFs: Ensuring quality for your clinical trial results
The significance of electronic case report forms in clinical trials for data accuracy and efficiency.