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    Generative Ai In Drug Regulatory Affairs

    Posted By: ELK1nG
    Generative Ai In Drug Regulatory Affairs

    Generative Ai In Drug Regulatory Affairs
    Published 10/2024
    MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz
    Language: English | Size: 677.54 MB | Duration: 1h 49m

    Top 5 Use Cases in Regulatory Affairs for application of Generative AI

    What you'll learn

    Application of Generative AI in Drug Regulatory Affairs

    Generative AI Fundmentals

    Use of ChatGPT for Text Processing Based Operations

    Implementation Details of Generative AI Applications

    Requirements

    Foundational Understanding of Drug Regulatory Affairs

    Description

    In this comprehensive tutorial, you will explore the cutting-edge application of Generative AI within the drug regulatory affairs landscape. This course dives into real-world use cases, including:Regulatory Intelligence: Automating the analysis of regulatory trends and gathering insights.Content Creation: Streamlining the generation of regulatory submission documents, labels, and reports.Language Translation: Enhancing multilingual submissions and compliance documents with AI-powered translation tools.Named Entity Recognition (NER): Extracting critical information from large datasets to improve efficiency in compliance and submissions.Data Analysis: Leveraging AI for advanced analysis and insights from clinical trials, safety data, and regulatory submissions.Besides, it will also cover use cases related to personal productivity and productivity at workplace. Amongst other topics, it will try to explain in brief, some foundational concepts of the technology behind Generative AI, products available in the market and capabilities of Generative AI in general.This course includes quiz assignments, mini-project tasks, and real-time examples to reinforce learning and allow you to practice applying these AI techniques in regulatory affairs scenarios. By the end of the course, you’ll be able to identify high-impact areas for AI implementation in drug regulatory processes.Disclaimer:This training is for educational purposes only. Learners should exercise due diligence before applying any concepts in real-time business environments.

    Overview

    Section 1: Introduction

    Lecture 1 Introduction

    Lecture 2 What to Expect from the Tutorial

    Section 2: Let's Set the Foundations of Generative AI

    Lecture 3 What is Generative AI?

    Lecture 4 AI Vs Generative AI

    Lecture 5 Technology Behind Generative AI

    Lecture 6 Generative AI Products in the Market

    Lecture 7 How to find Use Cases for Generative AI Application

    Lecture 8 Content Creation in Regulatory Affairs

    Section 3: Regulatory Intelligence using Generative AI

    Lecture 9 Introduction - What is Regulatory Intelligence?

    Lecture 10 Generative AI for Regulatory Intelligence

    Lecture 11 Demonstration of Regulatory Intelligence with ChatGPT

    Lecture 12 Demonstration of Building a Custom GPT

    Section 4: Regulatory Translation Using Generative AI

    Lecture 13 Introduction - Language Translation in Regulatory Affairs

    Lecture 14 Translation Capability of Generative AI

    Lecture 15 Demonstration of Translation using Generative AI

    Lecture 16 Evaluation of Language Translation

    Lecture 17 Reverse Translation and Evaluation

    Section 5: Named Entity Recognition using Generative AI

    Lecture 18 Introduction - Named Entity Recognition (NER) in Drug Regulatory Affairs

    Lecture 19 Named Entity Recognition - Traditional vs Gen AI approach

    Lecture 20 Demonstration of Named Entity Recognition using ChatGPT

    Section 6: Implementing a Generative AI Solution

    Lecture 21 Solution Implementation Approaches

    Lecture 22 Step by Step Approach for Developing a Generative AI Solution

    Lecture 23 Fine tuning a Model

    Lecture 24 Integrating with Data Sources

    Section 7: Issues and Constraints with Generative AI Solutions

    Lecture 25 Issues with Generative AI - Hallucination

    Lecture 26 Creativity Vs Consistency - What's Important in Regulatory Affairs

    Lecture 27 Prompt Engineering - Remediating Hallucination

    Lecture 28 Content Grounding - Remediating Hallucination

    Section 8: Conclusion

    Lecture 29 Thank you

    Drug Regulatory Affairs Professionals,Pharmacovigilance Professionals,Pharmaceutical Professionals,IT Professionals working in Drug Regulatory Affairs