We are a leading UK and European drug safety provider offering detailed responsive solutions through strategic thinking to help “Pharma make sense of Drug Safety”. Our highly experienced team of Pharma experts understand, and are fully conversant with, the latest Pharma regulations. We are as a team committed and passionate about all that we do for our clients, working with you to achieve total compliance every step of the way, supporting and helping navigate the way through the regulations, ensuring that your data is correct, compliant and clean. We are partnered with Samarind Ltd and have their Regulatory Software Management System installed here at our offices, allowing us to offer a software solution that includes Regulatory, xEVMPD, Medical Devices, Drug Safety, Medical Devices, eCTD, EDM and Tracking, thus allowing our clients to have the full flexibility of using an established software system at a fraction of the cost of a full database purchase. The cost of using an outsourced resource is often less expensive and more economical than using high cost internal team members. Let PDS take the strain of one off projects or a whole host of projects while you get on with running your departments. We provide services within the sectors of: • Pharmacovigilance (including CT, Post Marketed and Device Vigilance) • Medical Information • Patient Information • Regulatory Services • XEVMPD and ISO IDMP management and support • Medical Writing The new ISO IDMP regulations are to be implemented by all Pharma companies, whether large or very small, in the very near future, is your business ISO IDMP ready? We have developed a Gap Analysis tool to help you understand how ready you are, please feel free to ask us about this to ensure that you are ready for the new regulation changes. Find out how we can benefit your business , call us on +44 (0) 1476 512395 or email info@puredrugsafety.com or go to our website www.puredrugsafety.com