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Validity : 14th Mar'24 to 24th Mar'24
Project Management can be a complicated process. This session removes the complications by highlighting three basic aspects of project management and providing ideas on successfully implementing each of those aspects. Understanding the Project: Many believe t ...
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.
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 ...
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 ...
Substandard medications, like counterfeit drugs, present a real and increasing danger both to patients and companies and require a proactive approach to stay ahead of these problems. Substandard product can exist even if the product itself is manufactured ac ...
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 ...
There are 3 types of 510(k) submissions that can be submitted – Traditional, Special, and Abbreviated. The 510(k) process is considerably more rigorous than it once was, because of the following: Several international standards recognized by the FDA have b ...