OPTIMIZE

YOUR DRUG DEVELOPMENT JOURNEY

PAREXEL® Clinical Development Optimization offers end-to-end, technology-enabled drug development services to accelerate and simplify study design, start-up, execution and submission.

Design
Start-up
Execute
Submit

Find out what your journey could look like with PAREXEL’s optimization innovations.

DESIGN

Commercialization and Outcomes Plan Regulatory Strategy Quantitative Clinical Development Protocol Optimization Country and Site Selection Risk Assessment

START-UP

Investigator Grants and Contracts Regulatory and Ethical Approval Site Regulatory Documentation Study T raining Clinical Path Management Clinical T rial Logistics

EXECUTE

Recruitment and Retention Payments Risk-Based Monitoring Data Surveillance T rial Management and Analytics Imaging and Spirometry

SUBMIT

Data Management and Statistics Aggregation Clinical Study Report Publications Study T ransparency and Disclosure Cross Data Analysis Regulatory Cloud