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"The global automotive aftermarket size is expected to reach USD 486.4 billion by 2025, expanding at a CAGR of 3.9% over the forecast period. Digitalization of auto repair and component sales, complemented by advanced technology incorporations in automobile aftermarket component manufacturing, is expected to benefit market expansion. Surging reception of semi-autonomous, electric vehicles, and hybrid and autonomous cars is further expected to bolster the new component market growth in the years to come. The market can be categorized, based on replacement parts, into tire, battery, brake parts, filters, body parts, lighting and electronic components, wheels, exhaust components, and turbochargers."

"The 'Global and Chinese Dry White Wine Industry, 2012-2022 Market Research Report' is a professional and in-depth study on the current state of the global Dry White Wine industry with a focus on the Chinese market. The report provides key statistics on the market status of the Dry White Wine manufacturers and is a valuable source of guidance and direction for companies and individuals interested in the industry. Firstly, the report provides a basic overview of the industry including its definition, applications and manufacturing technology. Then, the report explores the international and Chinese major industry players in detail. In this part, the report presents the company profile, product specifications, capacity, production value, and 2012-2017 market shares for each company. Through the statistical analysis, the report depicts the global and Chinese total market of Dry White Wine industry including capacity, production, production value, cost/profit, supply/demand and Chinese import/export."

Several medical devices use either off-the-shelf or custom software. A couple of guidance documents from FDA written almost a decade ago are the only official comments from FDA to assist manufacturers understand the current FDA requirements. Despite a long history of software usages in medical devices, there is significant confusion regarding updating software applications in new 510(k) devices and the additional testing requirements. The level of details expected in a 510(k) application is very different from what used to be 10 years ago. This webinar will discuss the structure and level of detail required in filing a 510(k) when a medical device is software or contains software.

The Office of Device Evaluation (ODE) receives approximately 6500 Premarket Notification (5100) submissions every year. Many of these submissions are incomplete or grossly inadequate, as they fail to contain the components necessary to allow substantive review of the submission and inappropriately consume Center resources. As a means to employ more effectively the Center's resources, the FDA has implemented procedures to ensure that 5 10Ks meet a minimum threshold of acceptability; otherwise the Center will refuse to accept the submissions for substantive review.