Our services

Project Management

• Clinical trial planning oversight
• Monitoring of strategy Development
• Design and maintenance timeline expectations
• Communicate with internal team members, the sponsor and other relevant subjects
• Assurance of compliance with GCP and other regulations and guidelines
• Preparation of progress and status reports
• Adverse Events tracking and management
• Internal and external regular meetings and communication, TCs
• Monitoring
• Efficient data flow
• Clinical trial materials management
• Ethics Committees and regulatory submission/approval tracking
• Quality assurance
• Audit Site preparation
• GCP and trial-specific trainings
• Consulting services