[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"doc-detail-145971-en":3,"doc-seo-145971-105":30,"detail-sidebar-cat-0-en-105":90},{"code":4,"msg":5,"data":6},0,"success",{"doc_id":7,"user_id":8,"nickname":9,"user_avatar":10,"doc_module":4,"category_id":11,"category_name":12,"doc_title":13,"doc_description":14,"doc_content":15,"file_id":16,"file_url":17,"file_type":18,"file_size":19,"view_count":4,"is_deleted":4,"is_public":20,"is_downloadable":20,"audit_status":20,"page_count":21,"language":22,"language_code":23,"site_id":24,"html_lang":23,"table_of_contents":25,"faqs":26,"seo_title":27,"seo_description":14,"update_tm":28,"read_time":29},145971,1099523885336,"Taylor Morgan","https://ap-avatar.wpscdn.com/davatar_276721f389ce27ea32af1340a28f341c",7,"Healthcare","2026 Training Calendar - Medical Device Regulatory Trainings","2026 Training Calendar outlines a structured schedule of medical device and IVD regulatory training sessions, covering compliance obligations, licensing documentation practices, and practical preparation for submissions. The program spans core topics such as medical device risk classification, ISO 14971 risk management, ISO 13485 quality management systems, and IEC 62304 software lifecycle compliance. Additional modules address biocompatibility and biological safety documentation, advertisement regulatory requirements, import/export obligations, sterilisation methods and validation, and post-market incident investigation with RCA and CAPA. Registration is provided for each session, with a notice that dates may be rescheduled by MDA.","2026 Training Calendar   \n* Please note that MDA has the rights to reschedule the date of training  \n27/01/2026  \n28/01/2026  \nCompliance with Licensing Requirements and Hands-on Efficient Way to Prepare MDA Documentation Submissions on Medc@st  \nFundamental Understanding of Medical Devices & IVDs  \nRegister Here  \nRegister Here  \nJanuary  \nDate  \nTopic  \nRegistration  \n10-11/02/2026  \nGDPMD Session 1: Regulatory Requirements, Compliance Assessment and Implementation  \nRegister Here  \nFebruary  \n07/04/2026  \n08/04/2026  \n21/04/2026  \nMastering Risk Classification and Grouping of General Medical Devices  \nMastering Risk Classification and Grouping of IVDs  \nTraining on ISO 14971: Medical Device Risk Management Principles and Application  \nRegister Here  \nRegister Here  \nRegister Here  \nApril  \n05/05/2026  \n12/05/2026  \n20/05/2026  \nTraining on Regulatory Requirements for Medical Device Advertisement  \nRegulatory Assessment of Biocompatibility Requirements and Biological Safety Documentation for General Medical Devices and In Vitro Diagnostic Medical Devices (IVDs)  \nSession 1: Import and Export of Medical Device Requirements  \nRegister Here  \nRegister Here  \nRegister Here  \nMay  \n| \u003Cbr>2026 Training Calendar |  |\n| --- | --- |\n| \u003Cbr>June\u003Cbr>\u003Cbr>July\u003Cbr>\u003Cbr>August\u003Cbr>\u003Cbr>September\u003Cbr>\u003Cbr>October\u003Cbr>\u003Cbr>November |  Date   Topic   Registration \u003Cbr>\u003Cbr>11/06/2026\u003Cbr>23/06/2026\u003Cbr>07/07/2026\u003Cbr>14/07/2026\u003Cbr>04/08/2026\u003Cbr>22-23/09/2026\u003Cbr>14/10/2026\u003Cbr>21/10/2026\u003Cbr>04/11/2026\u003Cbr>The Training on Post-Market Incident, RCA & CAPA\u003Cbr>Training on IEC 62304: Medical Device Software Lifecycle and Compliance\u003Cbr>Training on Assessment of Common Submission Dossier Template (CSDT) for General Medical Devices and IVDs\u003Cbr>Implementation of ISO 13485 – Quality Management System for the Medical Devices\u003Cbr>Training on Medical Device Sterilisation Methods, Validation and Regulatory Compliance\u003Cbr>GDPMD Session 2: Regulatory Requirements, Compliance Assessment and Implementation\u003Cbr>Session 2: Import and Export of Medical Device Requirements\u003Cbr>The Regulatory Training: Post Market Requirements\u003Cbr>The Training on Introduction of Medical Device Regulatory Framework in Malaysia\u003Cbr>Register Here\u003Cbr>egis er ere\u003Cbr>\u003Cbr>Register Here\u003Cbr>Register Here\u003Cbr>Register Here\u003Cbr>Register Here\u003Cbr>Register Here\u003Cbr>R t H \u003Cbr>* Please note that MDA has the rights to reschedule the date of training |","cbCaivDMtrYScKae","https://ap.wps.com/l/cbCaivDMtrYScKae","pdf",828796,1,2,"English","en",105,"# January\n# February\n# April\n# May\n# June\n## July\n## August\n## September\n## October\n## November","[{\"question\":\"What topics are included in the 2026 medical device and IVD training calendar?\",\"answer\":\"The calendar includes training on regulatory requirements and compliance assessment, documentation submission preparation, risk classification and ISO 14971, ISO 13485 quality management, IEC 62304 software lifecycle, biocompatibility and biological safety documentation, import/export requirements, and post-market incident management with RCA and CAPA.\"},{\"question\":\"How can participants register for the training sessions?\",\"answer\":\"Each listed session provides a “Register Here” option, indicating registration is available per topic and date.\"},{\"question\":\"Can the training dates change after publication?\",\"answer\":\"Yes. The calendar includes a notice that MDA has the rights to reschedule the date of training.\"}]","2026 Training Calendar - Medical Device Regulatory Trainings | PDF",1787733270,5,{"code":4,"msg":31,"data":32},"ok",{"site_id":24,"language":23,"slug":33,"title":13,"keywords":34,"description":14,"schema_data":35,"social_meta":85,"head_meta":87,"extra_data":89,"updated_unix":28},"2026-training-calendar-medical-device-regulatory-trainings","",{"@graph":36,"@context":84},[37,53,67],{"@type":38,"itemListElement":39},"BreadcrumbList",[40,44,47,50],{"item":41,"name":42,"@type":43,"position":20},"https://docshare.wps.com","Home","ListItem",{"item":45,"name":46,"@type":43,"position":21},"https://docshare.wps.com/document/","Document",{"item":48,"name":12,"@type":43,"position":49},"https://docshare.wps.com/document/healthcare/",3,{"item":51,"name":13,"@type":43,"position":52},"https://docshare.wps.com/document/2026-training-calendar-medical-device-regulatory-trainings/145971/",4,{"url":51,"name":13,"@type":54,"author":55,"headline":13,"publisher":57,"fileFormat":60,"inLanguage":23,"description":14,"dateModified":61,"datePublished":61,"encodingFormat":60,"isAccessibleForFree":62,"interactionStatistic":63},"DigitalDocument",{"name":9,"@type":56},"Person",{"url":41,"name":58,"@type":59},"DocShare","Organization","application/pdf","2026-08-26",true,{"@type":64,"interactionType":65,"userInteractionCount":4},"InteractionCounter",{"@type":66},"ViewAction",{"@type":68,"mainEntity":69},"FAQPage",[70,76,80],{"name":71,"@type":72,"acceptedAnswer":73},"What topics are included in the 2026 medical device and IVD training calendar?","Question",{"text":74,"@type":75},"The calendar includes training on regulatory requirements and compliance assessment, documentation submission preparation, risk classification and ISO 14971, ISO 13485 quality management, IEC 62304 software lifecycle, biocompatibility and biological safety documentation, import/export requirements, and post-market incident management with RCA and CAPA.","Answer",{"name":77,"@type":72,"acceptedAnswer":78},"How can participants register for the training sessions?",{"text":79,"@type":75},"Each listed session provides a “Register Here” option, indicating registration is available per topic and date.",{"name":81,"@type":72,"acceptedAnswer":82},"Can the training dates change after publication?",{"text":83,"@type":75},"Yes. 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