Navigating supply chains and product portfolios during a pandemic

The UK has long been recognised as one of the world's leading destinations for clinical research. Home to world-class universities, an integrated healthcare system and a thriving life sciences sector, it offers an environment that enables innovative therapies...

For companies manufacturing or importing medicinal products into the EU or UK, the role of the Qualified Person (QP) is a mandatory regulatory requirement. What exactly is a QP, and why is this role so important? What is the Role of a Qualified Person? A Qualified...

Successfully conducting a clinical trial in the UK extends beyond developing an Investigational Medicinal Product (IMP) and recruiting participants. Sponsors must also establish robust regulatory, quality, and operational processes to safeguard participant safety,...