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Graeme Ladds
With a career spanning more than three decades, Graeme has trained thousands of professionals worldwide in pharmacovigilance and regulatory compliance best practices.
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35+ years in pharmacovigilance, drug safety, and regulatory affairs
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Delivered 500+ training courses to over 5,000 professionals in 30+ countries
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Developed 100+ bespoke training programmes for top pharmaceutical companies and CROs
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Worked with eight of the world’s top ten pharmaceutical companies
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Conducted audits in 6 continents (face-to-face and remotely) and attended over 70 inspections globally
Sarah Collins
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17+ years in pharmacovigilance and medical information leadership
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PgDip in Pharmacovigilance, University of Hertfordshire
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Subject Matter Expert in literature search set-up and safety reporting plans
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Extensive experience in client onboarding and workflow optimisation
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Leader in company-wide training programme development
Ben Rees
Ben has led aggregate reporting, risk management planning, and signal detection initiatives for global safety teams, combining scientific expertise with practical regulatory insight.
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16+ years in aggregate report management, risk mitigation, and signal detection
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Expert in MedDRA coding, data analysis, and safety surveillance
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Experienced in regulatory risk communication and strategy
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MSc-qualified with a scientific and analytical background
Paul Gilbert
Paul has a proven track record in delivering high-quality pharmacovigilance services for both clinical development and post-authorisation programmes.
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25+ years in the pharmaceutical industry, majority in pharmacovigilance and medical services
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UK-registered pharmacist with broad regulatory and operational expertise
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Specialist in inspection readiness, SOP development, and service delivery expansion
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Proven success in managing global PV services for clinical and post-authorisation programmes
Manohar Bollineni
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12+ years in global pharmacovigilance leadership
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Expert in case processing, PADERs management, signal detection, and PSMF oversight
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Led automation projects improving turnaround times and reducing error rates
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Developed scalable operations for high-volume regulatory periods