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Big Data
Blockchain
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America
country usa
United States
country canada
Canada
country brazil
Brazil  | Portuguese
country maxico
Mexico |  Spanish
country latam
Latam
Europe |  German 
country benelux
Benelux
country nordic
Nordic
country Southern Europe
Southern Europe |  French
country dach
Germany & Austria |  German
country United Kingdom
United Kingdom & Ireland
country Switzerland
Switzerland |  German
Africa
Asia Pacific
country
Asean
country
Korea
country
China
country
Australia & New-Zealand
country
Japan  |  Japanese
country
Taiwan
India & Middle East
country India
India
country
Middle East
Global Site
< Digital Operations and Platforms /  Medical Devices

Post Market Surveillance

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Strengthened Post Market Surveillance efforts to ensure optimal operations, compliance to regulations and to address rising complaint volumes

Wipro provides a global delivery model for Post Market Surveillance activities (as regulated by FDA governed by 21 CFR Part 820.198 in the US and other Regional Regulatory agencies across the world) with Complaint Call Center and Global Complaints Management Center for complaints intake and registration, complaints processing including Good Faith Efforts, regulatory reporting, complaints investigation, resolution, complaint closure and CAPA worldwide. With timely submissions, our team of Registered Nurses and subject matter experts have the ability to cater to different product divisions, complexity, and category risks. Our flexible to scale solution can help Medical Devices organizations realize 25-40% savings in operational costs, enhanced efficiency in processes, increased productivity, improved service levels and business value with speedy and smooth transition.

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