Pharmora can help throughout the lifecycle of drug development and post-marketing, having expertise across all phases and requirements. We have individuals and teams available to provide flexible and dedicated resources at your convenience. We 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 training on research techniques and pharmacovigilance either at our Macclesfield training centre or in-house. We can also help you improve your existing procedures and ensure you are prepared for a pharmacovigilance inspection.