List of Webinarhttp://www.panelcompliance.com/control/webinars_homeList of WebinarPanelCompliance Membership Planhttp://www.panelcompliance.com/control/w_product/~product_id=1003LIVETesthttp://www.panelcompliance.com/control/w_product/~product_id=1001LIVE6-Hour Virtual Seminar on Effective Technical Writing in the Life Scienceshttp://www.panelcompliance.com/control/w_product/~product_id=54726LIVEThis virtual seminar will begin with a general discussion of technical writing and its role within the life sciences.Excel Made Easy - Essential Functions to Work Smarter Every Dayhttp://www.panelcompliance.com/control/w_product/~product_id=54671LIVEOption 1 - Accuracy and Function Control Focus: Precision matters when working with complex formulas and data logic.Using ChatGPT with Excelhttp://www.panelcompliance.com/control/w_product/~product_id=54538LIVEThis course is designed to teach learners how to use CHATGPT for Excel, a powerful tool that can help you automate tasks, analyze data, and create reports in Excel. Throughout the course, learners will explore the features and capabilities of CHATGPT for Excel, like basic navigation and data import/export."If It Isn't Written, It Didn't Happen": Building Defensible Evidence Trails - Creating Contemporaneous, Inspection-Ready Documentation That Proves Controlhttp://www.panelcompliance.com/control/w_product/~product_id=54700LIVEIn regulated life sciences environments, documentation is more than a formality - it is proof. Whether demonstrating GMP compliance, validating a system, responding to a deviation, or defending decisions during an inspection, organizations must be able to show objective evidence that activities were performed correctly and at the appropriate time.Using CoPilot with Excelhttp://www.panelcompliance.com/control/w_product/~product_id=54539LIVEThis course is designed to teach learners how to use COPILOT for Excel, a powerful tool that can help you automate tasks, analyze data, and create reports in Excel. Device Changes, FDA Changes, and the 510(K)http://www.panelcompliance.com/control/w_product/~product_id=54654LIVEThis webinar will provide valuable guidance to regulated companies in development and implementation of formal, defined, documented methods for analysis of product changes and when to file a new 510(k). Computer Software Assurance (CSA): Building Risk-Based Validation for AI, SaaS and Digital Tools Moving from Documentation Burden to Evidence of Assurancehttp://www.panelcompliance.com/control/w_product/~product_id=54701LIVELife sciences organizations increasingly depend on digital technologies to manage manufacturing, quality, laboratory, and clinical operations. Cloud platforms, SaaS applications, automation tools, and AI-enabled analytics systems now play critical roles in ensuring product quality and patient safety.Using Claude to be More Productive in Excelhttp://www.panelcompliance.com/control/w_product/~product_id=54761LIVEThis course is designed to teach learners how to use CLAUDE for Excel, a powerful tool that can help you automate tasks, analyze data, and create reports in Excel. Master Hidden Features to Transform Your Word Documentshttp://www.panelcompliance.com/control/w_product/~product_id=54672LIVEOption 1: Unlock the potential of Microsoft Word in this insightful webinar that explores powerful yet often overlooked features to boost your productivity and document design.Data Integrity: Compliance with 21 CFR Part 11, SaaS-Cloud, EU GDPRhttp://www.panelcompliance.com/control/w_product/~product_id=54476LIVEThis webinar describes exactly what is required for compliance with Computer Software Assurance guidance, 21 CFR Part 11, and the European equivalent Annex 11 for local, and SaaS/Cloud hosted applications. Microsoft AI and Automation for Adminshttp://www.panelcompliance.com/control/w_product/~product_id=54740LIVEThis webinar equips admin professionals with critical insights into optimizing workflows using Microsoft AI tools. Explore practical automation solutions that can save you time, reduce errors, and enhance workplace productivity.50 Ways to Speed Up Instructional Design with AIhttp://www.panelcompliance.com/control/w_product/~product_id=54741LIVEIn this session, we’ll explore how AI chatbots are transforming instructional design, making the entire process faster, more creative, and more effective.Using a Learning Management System (LMS) to Develop Pharma Training Curriculahttp://www.panelcompliance.com/control/w_product/~product_id=54806LIVELearning Management Systems (LMSs) are important tools for assuring and demonstrating that Pharma employees maintain their training, and their GMP compliance, up to date. They often boast great functionality but also have limitations that must be overcome for a Pharma company to use them effectively. 6-Hour Virtual Seminar on The Use of Drug Master Files and Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities http://www.panelcompliance.com/control/w_product/~product_id=54733LIVEThis combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.Human Error Reduction Techniques for Floor Supervisorshttp://www.panelcompliance.com/control/w_product/~product_id=54714LIVESupervision plays a crucial role in Human Error Reduction and Control. Mastering Outlook Calendars, Contacts, and Foldershttp://www.panelcompliance.com/control/w_product/~product_id=54673LIVEStop wrestling with clunky calendars and overflowing inboxes. Whether you're coordinating global teams or just trying to find that one email, this session will turn Outlook into your ultimate productivity ally.ChatGPT and CoPilot for HRhttp://www.panelcompliance.com/control/w_product/~product_id=54540LIVEThis course is designed to equip HR professionals with the tools and know-how to harness Microsoft 365 Copilot and ChatGPT to help with HR tasks. Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Tech. Doc, n Files - The US FDA and EU MDR Rqmtshttp://www.panelcompliance.com/control/w_product/~product_id=54655LIVEThis webinar will examine the existing requiements for theUS FDA's DHF - including its derivitive documents, the DMR and DHR, and the identical ISO 13485 7.3 DandDF.