Udemy – Regulatory Affairs CMC



Last updated 6/2022
MP4 | Video: h264, 1280×720 | Audio: AAC, 44.1 KHz
Language: English | Size: 294.74 MB | Duration: 0h 51m
Chemistry, Manufacturing and Controls. From RA History to Submission.


What you’ll learn
Identify the CMC information required for submissions to support clinical studies and marketing applications
Discuss the role of ICH and individual national/regional guidances that should be referenced when preparing or updating a CMC section
Identify CMC changes that require agency notification
Be an expert in the main CMC-guidances
Requirements
Previous regulatory affairs, quality, clinical, R&D experience is a plus, but not strictly required
Description
This course provides an overview of the Chemistry, Manufacturing and Controls (CMC) section of dossiers and discusses CMC information necessary to support product applications, identifies CMC changes that are required for amendments, and provides an understanding of the CMC information needed to support marketing applications and postapproval submissions, including the use of Drug Master Files (DMFs) and CMC for IMPD. The best choice for future certification and career promotion. In general, despite regional differences, most health authorities expect an increasing amount of information and a depth of technical knowledge to be provided in clinical trial applications, CTD/eCTD dossiers. Regulatory requirements for CMC information, history of CMC, guidance, and tips are provided within the scope of this course. Creator of this course – D. Ladanovska (RA Consultant, Head of RA)Speaker of this course – Liyonish (US singer, actress, speaker) Upon completion of this course, you will be able to:Identify the CMC information required for submissions to support clinical studies and marketing applications;Discuss the role of ICH and individual national/regional guidances that should be referenced when preparing or updating a CMC section;Identify CMC changes that require agency notification;Explain different types of postapproval submissions;Describe the use of Drug Master Files (DMFs);Use tips for the IMPD Quality part;Be an expert in the main CMC-guidances. With a calm invited narrator’s voice in this course, be ready to expand your knowledge and be prepared for future career challenges and winnings. Let’s go!
Overview
Section 1: Introduction
Lecture 1 Greetings
Lecture 2 Introduction
Section 2: What is CMC?
Lecture 3 What is CMC?
Lecture 4 Application
Section 3: Regulatory History of CMC
Lecture 5 Regulatory History of CMC (1862)
Lecture 6 1883 – 1906
Lecture 7 1938
Section 4: EU Legislation
Lecture 8 EU Legislation
Section 5: ICH
Lecture 9 ICH
Section 6: Pharmacopeial Standards
Lecture 10 EU
Lecture 11 USA and Japan
Section 7: CMC Within A Drug Application
Lecture 12 CMC Within A Drug Application
Section 8: CMC Module 3
Lecture 13 CMC Module 3
Lecture 14 Dossier and Quality
Lecture 15 GMP guidelines
Lecture 16 QMS
Section 9: Up-to-date CMC
Lecture 17 Up-to-date CMC
Section 10: Procedure of Changes
Lecture 18 Procedure of Changes
Section 11: CMC-Guidances
Lecture 19 CMC-Guidances
Lecture 20 25 Tips for IMPD
Lecture 21 CMC planning for biologics application
Section 12: Summary of the course
Lecture 22 Importance
Lecture 23 Planning Strategies
Regulatory Affairs Officer,Regulatory Affairs Associate,Regulatory Affairs Specialist,Regulatory Affairs Manager,Quality Control Manager,Head of Regulatory Affairs,Regulatory Writer

Homepage

https://www.udemy.com/course/regulatory-affairs-cmc/

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