Successful programme and project management of biopharmaceutical,  pharmaceutical, healthcare, over-the-counter (OTC), and medical device products requires a unique blend of technical, scientific, regulatory, and quality skills to ensure focus and delivery of those critical activities that will directly impact the product registration and approval.

Often the commercial success of a project depends on the effective management throughout the clinical, product development, commercialisation, and licensing stages. Many companies find they lack the blend of skills within their own resource pool to manage this complex blend of activities.