Specialist Pharmacovigilance Course UK
One of the most experienced pharmacovigilance and pharmacoepidemiology experts in the world.
Professor Saad Shakir
Global Expert in Pharmacovigilance & Pharmacoepidemiology
★★★★★
“Collaborating with Professor Saad Shakir at Adroit Vigilance has significantly benefited our organisation. His pharmacovigilance and pharmacoepidemiology expertise deepens our drug safety understanding and fosters team adaptability. His guidance enhances patient outcomes and ensures proactive industry responses. We value his impactful commitment to excellence.”
– Dr. Edmund Burke
Pharmacovigilance Course UK
Pharmacovigilance Course UK
Pharmacovigilance Course UK
Professor Saad Shakir is a recognised authority in pharmacoepidemiology and drug safety, with international standing in pharmacovigilance, regulatory governance, and risk management. He delivers a specialist Pharmacovigilance Course in the UK through Pharmacovigilance Training UK, supporting pharmaceutical companies, regulators, and healthcare organisations operating across the UK, Europe, and global markets.
His distinguished career includes senior roles within the UK regulatory authority, GSK, and RPR, followed by his appointment as Director of the Drug Safety Research Unit in Southampton. In June 2025, he established an independent consultancy, offering expert drug safety advisory services alongside advanced Pharmacovigilance Course in the UK programmes and tailored international training solutions.
Through Pharmacovigilance Training UK, Professor Shakir addresses complex drug safety challenges, including product withdrawals, risk management planning, regulatory submissions, and the implementation of large-scale pharmacovigilance systems. His approach integrates clinical expertise with advanced epidemiological methods, supporting post-authorisation safety studies, real-world evidence generation, and robust risk minimisation strategies, underpinned by in-depth knowledge of UK, EU, and international regulatory frameworks.
Professor Shakir provides strategic oversight for safety submissions and regulatory responses, working closely with multinational pharmaceutical organisations as well as mid-sized and emerging life sciences companies in the UK and internationally. He has extensive experience collaborating with regulatory agencies and global institutions, serving as Chair or member of Safety Advisory Boards and Data Safety Monitoring Committees.
A prolific author, he has published widely in peer-reviewed journals, book chapters, and conference proceedings covering pharmacovigilance, pharmacoepidemiology, and drug safety risk management. He also serves on editorial boards for leading publications, including Drug Safety and Pharmacoepidemiology and Drug Safety.
Committed to advancing global standards in medicine safety, Professor Shakir delivers a leading Pharmacovigilance Course in the UK and internationally, and is a regular speaker at scientific and regulatory conferences, promoting best practice, regulatory compliance, and excellence in pharmacovigilance and pharmacoepidemiology.
Professor Saad Shakir
MB ChB, LRCP&S FRCP FISPE MRCGP
Global Drug Safety Consultancy & Pharmacovigilance Course UK
Pharmacovigilance Course UK
Saad Shakir is a highly regarded authority in pharmacoepidemiology and drug safety, internationally recognised for his expertise in pharmacovigilance, regulatory drug safety, and pharmacoepidemiology across the UK, Europe, the United States, and global markets. He provides specialist consultancy services and delivers a leading Pharmacovigilance Course in the UK through Pharmacovigilance Training UK, supporting pharmaceutical companies, life sciences organisations, and regulatory stakeholders in achieving operational excellence, regulatory compliance, and best practice in drug safety.
His distinguished career includes senior leadership positions within the UK regulatory authority, GSK, and RPR, followed by his role as Director of the Drug Safety Research Unit in Southampton. This extensive background spans regulatory, commercial, and academic environments and is underpinned by in-depth knowledge of UK, EU, US, and international regulatory frameworks relevant to organisations operating across Europe and beyond.
In June 2025, Saad established his independent consultancy, Adroit Vigilance, providing expert pharmacovigilance advisory services, advanced professional training programmes, and strategic drug safety support. Through Pharmacovigilance Training Europe, he works closely with organisations delivering a comprehensive Pharmacovigilance Course in the UK, helping to strengthen pharmacovigilance systems, enhance regulatory compliance, and implement robust risk management strategies aligned with UK, EU, and global regulatory requirements.
Our Services
Drug safety is essential for protecting patient wellbeing and maintaining trust in healthcare systems. Pharmacovigilance Training UK delivers a specialist Pharmacovigilance Course in the UK, equipping organisations with the skills required to monitor and assess adverse drug reactions, conduct comprehensive risk evaluations, and implement effective risk minimisation strategies in line with UK, EU, and international regulatory standards.
Through the systematic collection, analysis, and interpretation of safety data, the course enables early identification of medicine-related risks, supporting evidence-based clinical decisions and timely regulatory interventions. High-quality training provides healthcare and life sciences professionals with practical expertise to ensure the safe and appropriate use of medicines, prevent misuse, and uphold best-practice standards in pharmacovigilance.
By focusing on patient safety, regulatory compliance, and therapeutic effectiveness, the Pharmacovigilance Course in the UK helps improve patient outcomes and reinforces long-term confidence in pharmaceutical products and healthcare providers.
Consultancy & Advice
We provide expert consultancy and advice in the fields of pharmacovigilance and pharmacoepidemiology. Our services include:
Risk Management: We handle risk management and risk minimization, including monitoring its effectiveness.
Safety Studies: We conduct Real World Studies and PASS (Post-Authorisation Safety Studies).
Benefit/Risk Evaluation: We perform thorough benefit/risk evaluations.
Regulatory Submissions: We assist with pharmacovigilance submissions and responses to regulatory authorities.
ADR Assessment: We provide assessment of single and clusters of Adverse Drug Reaction (ADR) reports.
Specialised Boards: Saad is experienced in working with Data Safety Management Boards and Advisory Committees.
Medicolegal Work: We also undertake medicolegal work.
Training & Education
Our courses provide essential knowledge and practical skills for the safe handling, management, and administration of medicines. Through Pharmacovigilance Training UK, participants complete structured modules covering drug classifications, adverse effects, and best-practice guidance for storage, handling, and disposal. Learning is enhanced through expert-led sessions, real-world case studies, and practical exercises, enabling attendees to identify, assess, and mitigate medication-related risks across diverse settings. Strong emphasis is placed on regulatory compliance, ethical responsibility, and patient safety, equipping healthcare professionals, pharmacists, and medicines management teams with the confidence to uphold the highest standards of care.
We are committed to training and education on a wide range of topics in pharmacovigilance and pharmacoepidemiology. Our training is delivered through various formats:
Delivery Methods: Training can be delivered online, hybrid, or face-to-face.
Training Options: We offer in-house training, specific training courses, and conferences.
Collaborative Projects
As a recognised authority in pharmacoepidemiology, we actively engage in international collaborative programmes designed to advance pharmacovigilance standards and enhance patient safety. Through Pharmacovigilance Training UK, we deliver a comprehensive Pharmacovigilance Course in the UK that promotes innovation in drug safety, reinforces regulatory best practice, and ensures consistent compliance across complex UK, European, and global regulatory frameworks.
Our work through Pharmacovigilance Training UK supports organisations in developing robust safety systems, strengthening risk management processes, and facilitating evidence-based regulatory decision-making. By sharing global expertise and practical insights, we enable healthcare and life sciences organisations to improve patient outcomes and uphold the highest standards of drug safety across the UK, Europe, the USA, and international healthcare markets.
For general enquiries about AdroitVigilance and our services or courses, please fill out the form provided.
If you wish to engage Professor Saad Shakir, a leading pharmacoepidemiology consultant, for specialist advice, speaking engagements, or a Pharmacovigilance Course in the UK, please complete the enquiry form. For urgent matters, Professor Shakir can also be contacted directly using the details provided, though response times may vary due to international professional commitments.
To ensure the most effective support, we recommend providing your objectives and requirements in as much detail as possible. Alternatively, you may contact us by email or telephone to arrange a consultation or a tailored Pharmacovigilance Course in the UK delivered by an experienced pharmacoepidemiology specialist.