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This two day interactive seminar will focus on: Complaint Management Medical Device Reporting (MDR) EU Vigilance Reporting Product Recalls This course will provide practical guidance and real life examples that will help you develop and/or optimize your company’s post market surveillance system. Learning Objectives : Key goal of this course is to understand: Legal authorities (statutes and regulations) and definitions applicable to key elements of Post Market Surveillance (Complaint Management, MDRs, Vigilance and Product Recalls) Regulatory and compliance requirements related to each element of Post Market Surveillance (Complaint Management, MDRs, Vigilance and Product Recalls) Implementing applicable processes and procedures for Complaint Management, MDRs, Vigilance and Product Recall…






