“Just say what you do and do what you say” and just as importantly “write down what needs to be done and do what it says.” Patient safety, product quality and efficacy, and compliance are key in a life sciences environment. In addition, (bio-)pharmaceutical organizations strive for optimal business efficiency and product release time. Quality plays an essential role in achieving these objectives. Auditors assess whether organizations adhere to their agreements and regulations and whether there is a quality unit that is independent of production. Progress supplies specialists and project managers who can support you in implementing or improving quality (management) systems and processes and increasing staff awareness of all quality aspects. Our seasoned consultants have the latest knowledge of applicable current cGMP and other regulations and can guide you before, during and after inspections. We also offer interim quality personnel at every level and for operational departments (Interim Management – Progress (progress-lifesciences.nl).