Pharmacovigilance Solutions
Products
Information
Drug safety services provided from clinical through post-approval We offer a full suite of PV services helping clients around the world improve patient health and safety from clinical development through post-approval. We are equipped to expand as your business grows and our global team is prepared to handle large case volumes. Our team of qualified experts, combined with integrated technology, ensure your product meets the highest levels of compliance with both regional and global regulations. Safety Management Plan Development - Clinical & Postmarketing PV Auditing - QPPV & LPPV Services - ICSR Processing Submission & Reporting - PSMF Development & Maintenance RMP Development & Maintenance - Global & Local Literature Screening- Signal Management
Main Categories
BiopharmaceuticalsContract Services - Analytical & Lab Services
All Categories
BiopharmaceuticalsClinical Data ManagementConsulting ServicesContract Services - Analytical & Lab ServicesPatient Safety MonitoringPharmacovigilanceTechnology and software
Distribution areas
OceaniaNorth America (USA, Canada)AfricaMiddle East Region (e.g. UAE)Central America (e.g. Mexico)East Asia (e.g. China, Japan, Korea)Europe - EU countriesEurope - non EU (e.g. UK, Russia, ex-CIS countries)South America (e.g. Brazil, Colombia)South Asia (e.g. India, Pakistan, Sri Lanka)
