| Greetings!
Kickstart your journey in Regulatory Affairs with AAPS Pharma. This introductory workshop provides a clear, practical understanding of Regulatory Affairs in the healthcare industry, focusing on the drug development process and new drug submissions. Participants will explore the steps involved in obtaining drug approval, including notice types, priority review policies, and the importance of pre-submission meetings. The session also covers submission formatting and screening, highlighting the Common Technical Document (CTD) and the advantages of electronic CTD (eCTD) submissions. By the end of the workshop, attendees will have a strong grasp of the regulatory landscape and the essential components of drug submissions.
This workshop is ideal for individuals new to Regulatory Affairs or those seeking to strengthen foundational knowledge. It is particularly relevant for professionals in the pharmaceutical industry, including regulatory affairs specialists, drug development personnel, quality assurance staff, and anyone involved in the submission and approval of new drugs.
Participants will leave with the ability to understand regulatory submission requirements, navigate the new drug submission process, comprehend critical steps in drug development, and utilize CTD and eCTD effectively. Don’t miss this opportunity to gain practical, actionable insights that can advance your career in Regulatory Affairs.
Reserve your spot today and take the first step toward mastering Regulatory Affairs. | 
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