Last updated 1/2021 MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz Language: English | Size: 325.44 MB | Duration: 0h 45m Expand your opportunities and CV
What you'll learn How to create a registration dossier How to provide a qualified assessment of clinical documents How to develop an understanding of language fundamentals and style-guide conventions How to increase your salary Requirements No. You will learn everything from this course Description Regulatory Affairs & Medical Writing course provides a possibility to learn strategies, tricks, action plans to become confident in collaboration within a clinical and regulatory environment to create accurate, clearly worded documents. After this course, you will communicate simply and effectively. You will find detailed information about essential moments in regulatory affairs and current examples that will be helpful in dossier developing. Lecture about grammatical structure, professional literature, parts of the dossier Module 2 and template for clinical study report - are inside this course! Overview Section 1: Introduction and basics Lecture 1 Introduction Lecture 2 CTD-peculiarities Section 2: Regulatory medical writing Lecture 3 Set goals and collaborate Lecture 4 Tips and tricks Lecture 5 Parallel structure of writing Section 3: M2 developing - 2.5, 2.7 Lecture 6 Clinical Overview Lecture 7 Clinical Summary Section 4: Create your first Clinical Study Report Lecture 8 Module 5: strategy & action plan Section 5: Salary and growth Lecture 9 Increase your salary Section 6: Congratulation on your graduation! Lecture 10 Final words and reward Regulatory Affairs Managers,Regulatory Affairs Specialists,Medical Writers,Students