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Mawdsleys understand that pharmaceutical and biopharmaceutical companies need to know their Pharmacovigilance (PV) and Medical Information (MI) are being managed correctly and efficiently. A key part of Mawdsleys’ Regulatory Services, our Pharmacovigilance Service offer an accurate and competitive Adverse Event Reporting (ADR) system. By partnering with Mawdsleys clients will also get access to a wide range of services for all stages of the product life cycle.
Mawdsleys can take away the pressure by supporting pharmaceutical and biopharmaceutical companies with all pharmacovigilance needs:
Helping ensure patients have access to the drugs they need, when they need them.
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