Current Edition

ICH

Medical Writing – Benefit of Good Medical Writing

Knowledge is vital at every stage of a medicine’s lifecycle – from that first glint in the scientist’s eye at their origin to the delivery …

Continue Reading →
clinical trials

The Role of The Falsified Medicines Directive and Delegated Regulation in The Supply Chain of Clinical Trials

Companies providing clinical trial supply services to sponsors and contract research organisations (CROs) need to comply with a complex framework of regulatory requirements and industry …

Continue Reading →