CERTIFICATE COURSE IN DRUG REGULATORY AFFAIRS
Certificate course in Drug Regulatory Affairs from SG Pharma Training
If you want to start your career in regulatory affairs, a certificate course in drug regulatory affairs will help you land your dream job. At SG Pharma training, we provide premium courses. This certification will give you the knowledge and practical skills required to crack regulatory affairs interviews
Introducing our comprehensive Certificate Course in Drug Regulatory Affairs, designed to equip you with the knowledge and skills needed to navigate the complex world of regulatory requirements.
In this course, you will explore regulatory frameworks for key markets including the US, EU, and Rest of the World (ROW), covering topics such as:
🔹 US Submission Process: Understanding USFDA and its workings, types of Drug Master Files (DMFs), CTD format, and more.
🔹 EU Submissions Demystified: Delve into EMA, centralized vs. decentralized submissions, ASMFs, COS filings, and EDQM procedures.
🔹 Insight into Health Authorities: Learn about different health authorities, their roles in drug registration, and the CTD format.
🔹 eCTD Preparation: Master the art of preparing dossiers and DMFs in electronic Common Technical Document format.
🔹 Indian Regulatory Landscape: Understand the functions of DCGI, CDSCO, and the submission procedure in India.
🔹 International Guidelines: Explore ICH guidelines and cGMP standards crucial for regulatory compliance.
Our expert-led course offers in-depth insights, practical knowledge, and real-world case studies to ensure you are fully equipped to excel in the regulatory domain.
So, start your journey towards your dream job by enrolling in our course, remember only limited seats available, and you will be shocked to see the course Price.
Enroll now and take the first step toward a rewarding career in Drug Regulatory Affairs!