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Validity : 14th Mar'24 to 24th Mar'24
The ability of artificial intelligence/machine learning software to learn from real-world feedback and improve its performance is spurring innovation and leading to the development of novel medical devices. The FDA recognizes AI's advantages and risks and has ...
This training on FDA software validation and verification will provide you with the best practices necessary to ensure that all systems are validated in compliance with FDA regulations.
There is a skill and art to understanding each employee’s motivation and learning to leverage their talents. This course will explore how to better understand what motivates your employees, and develop a variety of strategies to keep them engaged and productiv ...
Work Smarter means realizing that effective delegation is a critical factor for operational efficiency in all organizations in today's dynamic and highly changing and competitive business environment. Yet 65% of the managers Gallup studied had limited-to-low l ...
No matter what job you hold, special projects crop up. Knowing how to best manage them is key to their success. Using tips and techniques, like the 7 P’s, can help guide you to a smooth flowing project. This course will review the areas of project management t ...
There are new roles that require a thorough understanding of functional interrelationship if you are to succeed. This presentation identifies the elements needed to provide a business with best materials and/or service. Understand how to bring together the ...
The training on "FDA 483 or Warning Letter - Now What?" is a comprehensive program designed to equip professionals in FDA-regulated industries with the knowledge and skills needed to effectively navigate and respond to regulatory challenges. When faced with an ...
"Excel: The Power of Color" is a webinar that delves into the strategic use of color in Microsoft Excel to enhance data visualization and spreadsheet functionality. This topic explores how color can be used as a powerful tool to improve data comprehension, org ...
If you do any work that will be reported to the US Food and Drug Administration (FDA), Environmental Protection Agency (EPA), or Occupational Safety and Health Administration (OSHA), your work must be done under GLP. All methods must be validated, the proof t ...
Test method validation is an often-confusing requirement for medical devices. A fundamental issue is the role-reversal between the test method and the product or process it is designed to detect. For example, while a defect-free process is desirable, a test ...