Founded in 2002, we are a pharmacovigilance focused consultancy delivering advisory and outsourcing solutions to the bio-pharmaceutical and medical device sectors. We operate across the drug development and post marketing spectrum and have served more than 170 clients globally. Our experienced team of physicians, pharmacists and scientists is the key to our success, and our simple and transparent operating model routinely results in high levels of client satisfaction and repeat collaboration. We are based in Cheshire, UK with team members and consulting partners based in the US, mainland Europe and India.
We have a proud history of consulting with clients to help them overcome challenges...
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At DSSL, we offer flexible sourcing solutions to support your pharmacovigilance system..
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Audits and Inspections are an essential component of maintaining a PV system that is fit for purpose.
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We can provide pharmacovigilance training to your teams through our network of expert partners.
READ MOREWe 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.
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.
Irfan serves as the Managing Director of DSSL. He is a trained physician and holds a Master’s Degree in Molecular Medicine from University College London. He has over 18 years’ experience in the pharmaceutical industry, having worked in leadership roles for both large and medium-size biopharmaceutical companies, in clinical development and pharmacovigilance. This experience has resulted in his extensive knowledge and insightful understanding of the global pharmacovigilance and clinical development landscape.
He has hands-on expertise in formulating and applying best practices in pharmacovigilance across Europe/US/Japan and has been instrumental in driving a pro-active approach to patient safety and risk management globally.
Rob is an industry veteran; his experience includes leading pharmacovigilance operations groups for top 10 pharma and have provided consulting services to Regulatory Authorities. He is passionate about delivering patient safety through process design and technology and he has gained significant experience in traditional pharma products as well as the development of new wave products such as gene and cell therapies.
Maikel is a qualified nurse with over 14 years of experience in the pharmaceutical industry. Highly experienced in pharmacovigilance, case processing, and aggregate report writing, he has specialized in working for both marketed and under development product lines. In addition to his extensive in PV operations, he is a qualified auditor who has led global PV auditing programs. Having taken part and played critical roles in pharmacovigilance related projects. PV inspections, and audits, Maikel Hofwijks also serves as EU QPPV for several DSSL clients.
Rahul is a physician, who for more than 12 years has worked in Pharmacovigilance and clinical research. Rahul’s expertise includes safety review strategies, signal management, aggregate report writing, Risk Management Planning and Minimization activities, case processing and literature surveillance.
