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Taking care of all pharmacovigilance requirements.

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:


For more information pharmaceutical and biopharmaceutical  companies should e-mail info@mawdsleys.com

You may also be interested in: Third Party Logistics, Regulatory Services UK, QP Services, QP Batch ReleaseControlled Access Programmes, Clinical Trial  ServicesDrug Shortage Management

Helping ensure patients have access to the drugs they need, when they need them.

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