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QED adds Safety / Pharmacovigilance service offering

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QED adds Safety / Pharmacovigilance service offering

Demonstrating their appreciation of the critical importance of safety and pharmacovigilance in clinical trials, not just from a Regulatory standpoint, QED has today extended its service offering to include provision of extensive Safety and PV services, ranging from SAE & SUSAR reporting through to consultancy and training. QED’s expert Safety team can provide a centralized and highly coordinated service for global studies as well as drawing on local expertise on a country-by-country basis. Similarly to their wider service offering, QED are able to tailor their safety and PV service provision to each individual client ranging from handling high volumes of SAEs for large pharma sponsors through to acting as a complete Safety Department for smaller Biotech sponsors. QED’s Safety/PV team consists of highly experienced Senior Pharmacovigilance Specialists with on average more than 10 years industry experience