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Mapping and evaluating all the steps in a current pharmaceutical ingredient bulk manufacturing workflow can lead to valuable process improvements. In this webinar, we discuss how this review can be accomplished and the possible benefits that can result.
In this session, you’ll discover how Excel’s AI-powered features can supercharge your productivity: Work Smarter with Copilot – Generate formulas, summaries, and insights instantly. Analyze Data in Seconds – Ask questions in plain English and get ready-to- ...
Unlock Next-Gen Productivity: Learn how AI, particularly ChatGPT, is transforming the way professionals use Excel. Discover how to streamline workflows, reduce manual effort, and complete tasks faster than ever before. AI-Powered Formula Assistance: Understan ...
Discrete event simulation (DES) is the most powerful methodology used in process data analytics. The following examples will be covered: Outpatient clinic: centralized or separate locations? Outpatient clinic: non-steady-state operations, Outpatient Clini ...
Workplace drama sucks the productivity of teams and organizations. It also creates an inhospitable environment where healthy people don't want to work ... so they leave. Good, productive people leave the organization. In fact, the best people, the highest perf ...
This course concisely explains the latest "see, hear, speak" multi-modal updates to ChatGPT and how they can be used in an accounting context. New features include vision processing, voice conversation, image generation, real-time Internet access, advanced dat ...
This webinar will discuss the US FDA’s Final Guidance on the Q-Submission Program, dated May 29, 2025, which addresses how to request interactions with the FDA related to future medical device submissions. This allows companies and the FDA to arrive at mutual ...
In today's rapidly evolving regulatory landscape, organizations across industries are under increasing pressure to ensure compliance with a multitude of laws, regulations, and industry standards. Compliance audits play a vital role in assessing an organization ...
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.
This comprehensive course offers essential knowledge and practical skills in root cause analysis, corrective and preventive actions (CAPA), and conducting effectiveness checks. Participants will learn systematic approaches to identify root causes, develop effe ...