We believe that exceptional pharmacovigilance begins at the individual case report level with high-quality, consistent data capture and management practices. With today’s expanding regulations and growing enforcement, it is more important than ever to utilize proven methodologies and best-practices for managing your adverse event case load.
With Ashfield Pharmacovigilance, you have access to the tools and experience needed to provide a fully compliant drug safety program and a wide array of pharmacovigilance services. From clinical trials safety to post-marketing surveillance, Ashfield Pharmacovigilance manages data collection, triage, tracking, and reporting of your adverse events from start to finish.
Analyzing, assessing and reporting important safety data requires best practices for data entry, follow-up and query, quality control, medical review and quality assurance. Ashfield Pharmacovigilance adheres to industry-recognized best practices for data management, coupled with thoughtful, business metrics and workflow for enhanced efficiencies.
01 Jun 2015
Ashfield attended The World Drug Safety Congress Americas
The current pharmacovigilance landscape is defined by complex IT systems that require frequent...Read more
24 Jun 2015
Ashfield Pharmacovigilance has a unique advantage in drug safety and pharmacovigilance
Ashfield Pharmacovigilance has a unique advantage in drug safety and pharmacovigilance due to...Read more
Quality, Partnership, Ingenuity, Expertise, Energy
It’s not just what we do, it’s why we do it.