Cidal

CIDAL provides the following services in the organization and implementation of a Clinical Trial:

• Project Management
  Supervision, communication and tracking of Project activities
• Quality Assurance
  Internal process audits to ensure compliance with Good Clinical Practices and project SOPs
• Study Monitoring
  Experienced Clinical Research Assistants (CRAs) fully trained in FDA regulations, ICH guidelines and GCP/SOP compliance
• Research Site
  CIDAL physicians and scientists as Project Investigators or Sub-investigators
• Feasibility evaluations
• Pilot tests of study instruments and questionnaires
• Organization of Investigator Meetings
• Regulatory services and submission of proposals to local ethics committees and health authorities
• Study drug management
• Collection, processing and shipment of biological specimens to central laboratories
• Selection, hiring and supervision of clinical and imaging laboratories
• Legal and informal English-Spanish translations