Comprehensive support for clinical budgeting, compliance, contract management, and regulatory advisory to safeguard your research operations.
Design financial frameworks to optimize trial resources, control spending, and manage study budgets effectively.
Ensure all financial operations adhere to sponsor and legal requirements with detailed audit-ready documentation.
Draft, review, and negotiate agreements for sites, vendors, and third parties to ensure legal clarity and protection.
Consult on clinical trial agreements, intellectual property, and data protection laws including GDPR and PDPA.