This interactive webinar explains how to configure and validate GxP-compliant spreadsheet applications to avoid FDA 483s. Follow the step-by-step instructions as we configure Excel for audit trails, security features, and data entry verification. Understand ho ...
In this engaging and practical webinar, you’ll explore how Claude AI can support HR, people managers, and operations leaders in real-world scenarios. This is not a technical demo. Instead, you’ll see how AI can enhance communication, improve documentation, sup ...
You Have More HR Work Than Hours in the Day. Claude Can Help — If You Use It Right. Job descriptions to write. Resumes to screen. Performance reviews to draft. Difficult conversations to plan. Manager emails to soften before they hit "send." And then leaders ...
This interactive training class equips participants with the mindset, strategies, and tools to negotiate effectively in diverse professional settings. Learners explore the art of principled negotiation, uncover win-win solutions, and practice techniques for pr ...
HR documents carry real weight. A poorly worded job description affects who applies. A policy document that contradicts itself creates legal exposure. An onboarding guide that is out of date wastes new hire time. The stakes are high enough that most HR teams h ...
An OSHA inspection can put an employer’s safety program, documentation, and decision making under immediate scrutiny. Knowing what to expect and how to respond professionally can help an organization manage the process, protect its rights, and make informed de ...
What are the basics of an enterprise maintenance-focused Quality Management System? This webinar will examine that question by means of the international standard, ISO 9001, the international standard for Quality Management Systems for all business or industri ...
This course will teach how to conduct a software validation program for medical devices containing software that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation and how to use ISO62304 to establ ...
The majority of medical devices are cleared for marketing in the U.S. by the FDA under the 510(k) process. The FDA holds companies responsible for filing new 510(k)s when new products are to be marketed in the U.S., or when existing products and/or their Indic ...
