Pharmacy - Events
This webinar will help you understand the requirements of the new medical device regulation EU MDR 745/2017 and teach you how to create new required reports for the Notified Body and the Competent Authorities and how this process is connected to other processes in the quality management system according EN ISO 13485:2021. Why Should You Attend: You should attend this webinar to understand, what are the changes to the previous medical device regulation and how to implement the changes in your current quality management system according ISO 13485:2021 like post-market-surveillance plan and report and how to create the annual PSUR – Performance Safety Update Report to the Notified Bodies and EUDAMED in a simple and quick way. Your implementation need smart ideas to reach the right level to pa…
This seminar is based on FDA E6 GCP Guidelines which are the basis of effective data quality management. Even if your research is not FDA regulated, the information you learn in this course will help to ensure a robust data collection and management plan. Learning Objectives: Regulatory guidelines for Clinical Data Management Best practices for data collection CDISC/CDASH/STDM standards Responsibilities of personnel Case report form criteria Maintaining confidentiality of data Data storage and transferability Data preparation and quality assurance for accuracy Data monitoring plan criteria Data systems validation Adverse event reporting and coding criteria What to expect on a monitoring visit Troubleshooting and resolution of deviations from plan Who will Benefit: Study Investigators Da…



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…




Conrad Dubai, Sheikh Zayed Rd - Trade Centre - Trade Centre 1, Dubai, Dubai, United Arab Emirates
The 11th Annual MENA International Orthopaedic Congress has been developed to provide an innovative and comprehensive overview of the latest developments in the field of Arthroplasty, Spine, Trauma, Orthopaedic Oncology, Foot and Ankle, Podiatry, Sport Medicine, Arthroscopic Surgery and Sport Medicine. This year's conference theme will focus on the practical management and latest evidence-based clinical data that will highlight the most advanced strategies in detection, prevention and management of common orthopaedic conditions through the most advanced techniques. Expect to meet thought leaders, leading orthopaedic surgeons, government pioneers, academia, researchers and technology providers who will be sharing their knowledge in the format of presentations, discussions, workshops providi…