QVigilance is a Pharmacovigilance (PV) Service Provider that offers comprehensive PV and risk management services for Sponsors of clinical trials and Marketing Authorisation Holders. Use our pharmacovigilance services and expertise to meet all your clinical trial and post-authorisation needs as you remain compliant with your regulatory obligations and safeguard your patients and trial subjects through proactive continuous safety monitoring and proportionate risk minimisation of your medicinal products. Global Pharmacovigilance Services • PV Safety Database (Argus Oracle, v8.1.2) • Case Processing and Reporting • Global & Local Pharmacovigilance Literature • Aggregate Reporting • Signal Management • Risk Management • Regulatory Intelligence • Medical Device Vigilance • Pharmacovigilance Consultancy European Pharmacovigilance Services • Qualified Person for Pharmacovigilance (QPPV) • EudraVigilance submission and manteinance services • Pharmacovigilance System Master File (PSMF) Pharmacovigilance blog: http://qvigilance.com/blog White Papers & Webinars: http://qvigilance.com/pharmacovigilance-resources