What We Do Best
Programme Consultancy:
Strategic Planning
Investment (Private/Venture)
Grant Funding (H2020/EIS/NIH)
Pre-Clinical Requirements (Toxicology/ADME)
Regulatory (Liaison/Licensing/Submission)
Experimental Design
IMP Drug/Device Management (GMP/Importing)
Clinical Oversight
Project Management
Site Selection/Initiation
Patient Recruitment
Implementation Of Infrastructure
Clinical Monitoring
Medical Review And Monitoring
Safety Monitoring -Pharmacovigilance
Data Management
Analysis And Reporting
Statistical Design
Development Of Analysis Plans
Programming And Analysis
ICH Reporting
Scientific Writing
Quality Assurance
Publications (Journals/Conference Presentations)