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Standard vs Accredited Calibration and Considerations in Choosing a Calibration Provider Monday, August 10, 2020
When it comes to equipment calibration services, you have options, which can make decisions a little complex. With that in mind, let’s break down the two most common options to get a better understanding of what they are and when they are necessary.   Properly calibrated instruments help increase confidence for those using the equipment. As a calibration provider, we deliver information about the …
5G communications testing and calibration from Tektronix
As 5G Advances the Need for Equipment Calibration and Maintenance Accelerates Tuesday, July 21, 2020
The promise of 5G is drawing near and will bring about many changes throughout the next decade and will change the way we interact with technology on a day-to-day basis. With its ultra-fast speeds and unprecedented response times, the complex information that can be transmitted through 5G’s High Band frequencies has the potential for and virtually unlimited possibilities for growth and advancement …
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5 Hidden Costs of Using Low-Cost Calibration Providers Wednesday, July 15, 2020
Equipment calibration is essential to improving a company’s bottom line by minimizing the risk of product defects and recalls and enhancing a reputation for consistent quality. In its most basic form, calibration is the measuring of an instrument against a standard. As instruments become more complicated, successfully identifying and applying best practices can reduce business expenses and improve …
Avoiding Asset Management Pitfalls: Web-Based Solutions for Medical Device Manufacturers Thursday, May 18, 2017
Within any industry, combatting operational risk while balancing financial responsibilities are chief concerns. For medical device manufacturers, there is additional regulatory pressure to prove that assets are properly maintained and calibrated. In this post, we’ll identify three common asset management pitfalls experienced by medical device manufacturers and talk about how to build a strong …
Top Five Risks for Medical Equipment Calibration Programs Tuesday, April 4, 2017
The US Food and Drug Administration (FDA) consistently lists inadequate maintenance and calibration procedures as a top reason for issuing Form 483 observations to medical device manufacturers (hint: this is NOT a good thing). Within highly regulated industries, calibration program problems can leave you open to risks ranging from delays in time to market to increased liability and patient …
Helping medical device manufacturers stay in compliance with ISO quality standards and FDA regulations Wednesday, March 22, 2017
A recent meeting with a large medical device customer lead to an enlightening discussion on the differences between International Organization for Standardization (ISO) and US Food and Drug Administration (FDA) standards and regulations as they apply to medical device manufacturers. This is a short overview of a few of the key differences between ISO and FDA compliance and a quick guide to …

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