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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- ...
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals. The focus of most validation work is on the methodology, the standard operating procedure (SOP). But validat ...
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 ...
This webinar will explain the process of analyzing and minimizing cyber risks for premarket submissions. It will explain how cyber risks are identified and mitigated. Concepts from the 2025 Guidance will be explained. The cybersecurity program must be carefull ...
An external auditor is coming to your plant. Their first impression may have a major impact on your plant's future as well as your own career. How will your plant look to that auditor? Before they even set foot in the door - what your grounds and outside fa ...
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 ...
Accountability is the cornerstone of effective leadership, yet many leaders struggle to cultivate it within themselves and their teams. This webinar provides a clear, actionable blueprint to transform your approach. You'll move beyond the everyday frustration ...
As the pace of technological innovation and evolution becomes more intense, there is a critical need for computer system validation, 21 CFR Part 11 (Electronic Records and Electronic Signatures) compliance, and data integrity assurance to continue in environme ...
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 ...