WCT Drug Safety and Pharmacovigilance utilizes state of the art electronic methodology to provide superior safety oversight of clinical trials, while assuring strict compliance with all local regulations (FDA, EMEA) , international guidelines and best Pharmacovigilance practices (CIOMs). We process all SAEs in one business day via paper, remote and direct electronic entry using time and client honored methodology to ensure thorough and delimited follow-up through case closure.

• Medical monitor (physician) on call 24/7
• Processing of Serious Adverse Events and Communication to Sponsor within 1 business day
• Flexible Operational approaches
• - Industry-pioneering integration of SAE processing with Clinical EDC
• - Remote/direct electronic entry into Sponsor Safety Database
• CRF Safety and Lab Review
• SAE Reporting
• RiskMAP development
• Advanced Pharmacovigilance planning and Consultation