Thorough collection and assessment of product safety information is essential to the success of clinical research studies and maintaining post-marketing product licenses. To meet the increasingly complex and diverse global regulatory requirements, we offer a comprehensive suite of services designed to ensure safety while focusing on the rapid approval of your compound and pharmacovigilance monitoring thereafter. The team at Grand Pacific CRO focuses on transparency and easy to review outputs, with a strong focus on continuous quality improvement and operational efficiency.

Our safety and pharmacovigilance team operates globally and provides:

• Full safety service requirements including safety database
• Tailored solutions for commercial and academic research across all phases
• A service that is adaptable, yet able to maintain the highest regulatory and ethical compliance
• A thorough understanding of safety reporting requirements across trial countries