Global Compliance Seminar Information

We offer the opportunity to seek topics of special interest to the highly regulated healthcare industry. We provide customized webinars for FDA GLP, GCP, cGMP (QSR), 510(k), PMA, CE marking (MDD/AIMDD/IVDD), FDA BIMO inspection, MDR, labeling complaint handling system, and many more. The contents of our webinars are designed to help achieve compliance and remain compliant in the highly regulated healthcare industry. In particular, by focusing on aspects of global regulatory, quality, clinical, and compliance matters (drugs, biologics, biosimilars, and medical devices including in vitro diagnostic medical devices), we greatly help to facilitate marketing clearance or approvals of medical products while achieving compliance and increasing awareness. We strive daily to significantly improve patient safety, business practices, and public health.