{"id":165337,"date":"2019-08-19T10:24:05","date_gmt":"2019-08-19T10:24:05","guid":{"rendered":"http:\/\/www.georgianewsdesk.com\/news\/story\/165337\/medical-device-complaint-management-market-to-grow-at-102-billion-by-2026-key-players-iqvia-wipro-tata-consulting-services-sas-sparta-systems-and-parexel-international-corporation.html"},"modified":"2019-08-19T10:24:05","modified_gmt":"2019-08-19T10:24:05","slug":"medical-device-complaint-management-market-to-grow-at-102-billion-by-2026-key-players-iqvia-wipro-tata-consulting-services-sas-sparta-systems-and-parexel-international-corporation","status":"publish","type":"post","link":"http:\/\/www.honolulunewsnow.com\/news\/story\/165337\/medical-device-complaint-management-market-to-grow-at-102-billion-by-2026-key-players-iqvia-wipro-tata-consulting-services-sas-sparta-systems-and-parexel-international-corporation.html","title":{"rendered":"Medical Device Complaint Management Market to Grow at $10.2 Billion by 2026 | Key Players – IQVIA, Wipro, Tata Consulting Services, SAS, Sparta Systems and Parexel International Corporation"},"content":{"rendered":"
\"Medical<\/a><\/p>\n
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Grand View Research, Inc. – Market Research And Consulting.<\/div>\n<\/div>\n<\/div>\n
The global medical device complaint management market size was estimated at USD 5.37 billion in 2017. It is anticipated to register a CAGR of 7.6% during the forecast period<\/div>\n

The global medical device complaint management market<\/a> size is expected to reach USD 10.2 billion by 2026, according to a new report by Grand View Research, Inc. It is anticipated to register a CAGR of 7.6% during the forecast period. Increasing use of software to support the entire complaint management process is propelling the growth.<\/p>\n

The transition from paper-based to digital system for tracking complaints is boosting growth of the market. Incidents are recorded and the data automatically drives the investigation and resolution workflow. Companies experience more complete documentation along with the reduction in the turnaround time. The complaints management solution provides advanced analytics and reporting tools for augmented management oversight. The software also streamlines the submissions with standard reporting for the EU, FDA, Japan, Health Canada, and Australia.<\/p>\n

Request a Sample Copy of the Global Medical Device Complaint Management Market Research Report @<\/strong> https:\/\/www.grandviewresearch.com\/industry-analysis\/medical-device-complaint-management-market\/request\/rs1<\/a><\/p>\n

For instance, the U.S. FDA encourages consumers, patients, and healthcare professionals to give voluntary reports of important adverse events, and\/or product issues to MedWatch, FDA’s Safety Information and Adverse Event Reporting Program or by means of the mobile app known as MedWatcher. The app radically simplifies and accelerates the process of reporting by providing users with a four-step form submitted electronically to the FDA.<\/p>\n

Regulators are gradually concentrating on handling customer complaints, product safety, and device vigilance. This is not only true in developed countries, but also in emerging economies such as India. The Indian government introduced medical devices regulation program, Materiovigilance Programme of India (MvPI) with focus on safety data collection, synchronization of international laws, regulations, and standards encourages medical device organizations to evaluate their existing procedures of product development and post-marketing surveillance.<\/p>\n

\"U.K.<\/p>\n

Further key findings from the study suggest:<\/strong> <\/p>\n