• Phone: +44 (0)1476 570819
  • Email: bd@drugsafetysolutions.co.uk


Founded in 2002, we are a pharmacovigilance consultancy delivering advisory and outsourcing solutions to the bio-pharmaceutical and medical device sectors. We have operated across the drug development and post marketing spectrum and have served more than 170 clients globally. We have a dedicated team of physicians, pharmacists and scientists. Our experience is the key to our success, and using our simple and transparent model routinely results in high levels of client satisfaction. Our headquarter is in Cheshire, UK, and our team is based in Europe and India.


We offer high quality, value added solutions for global pre- and post-approval pharmacovigilance as well as related services in product safety such as clinical development, medical monitoring, medical information and regulatory services through our trusted partners.

We offer a full range of Pharmacovigilance and Product Safety services, including:

  • Provision of Qualified Person for Pharmacovigilance (QPPV) – local and EU
  • Set up and operation of PV System • Adverse Event processing Literature surveillance
  • Signal detection and evaluation
  • Aggregate Reports (PSUR/DSUR)
  • Risk Management and Minimization
  • Pharmacovigilance audits and inspection readiness activities
  • Registration to EudraVigilance and registration of products in xEVMPD
  • Safety Data Exchange Agreements (SDEA) preparation/review and mainte nance
  • Provision of pharmacovigilance training


DSSL’s knowledge is deep and varied, and the service is attentive and intuitive – they have a CAN-DO attitude.


Their collaborative approach is bespoke and client-centric. At every stage we were clear on who is doing what, when and how. The results speak for themselves.