Welcome to Pharmora
We provide specialist pharmacovigilance, drug safety, risk management and other pharmaceutical medical and regulatory expertise.
The word pharmacovigilance originates from the Greek word “Pharmakon”, meaning drug, and the Latin “vigilare”, meaning “to be awake or alert, to keep watch”.
Pharmacovigilance was defined by the World Health Organisation as “The science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem.” The aim is therefore to identify potential new hazards and prevent harm to patients, but there are many other ways it can add value for the brand and the company, and this continues right through the product life cycle.
Pharmora can help you plan, monitor and report safety data from the first clinical trial all the way to marketing authorisation of the product and beyond. We can help with licence-to-operate activities including routine submissions and ad hoc regulatory interactions. Pharmora can provide pharmacovigilance training in house to help you improve your existing procedures and ensure you are prepared for a pharmacovigilance inspection.
We hope you enjoy our website, why not use it to find out more about the services we offer, or you can get in touch via our contact form.