ERA | Excellence in Regulatory Affairs | Pharma Regulatory Services & Training

PROFESSIONAL TRAINING PROGRAM

Regulatory Affairs Training

ERA (Excellence in Regulatory Affairs) offers an industry-oriented Regulatory Affairs Training Program designed to provide detailed knowledge of regulatory concepts, pharmaceutical documentation and global product registration processes. The course starts with the fundamentals and gradually develops practical expertise in CTD dossier preparation, making students industry-ready in a short period of time.

Course Details

Instructor Experienced Trainers from Industry

Duration 2 Months

Weekend Batches All 4 Sundays

Class Timing 2 Hours / Class

Mode Online

Eligibility Students of B.Pharm (3rd & Final Year), M.Pharm, B.Sc. & M.Sc. (Life Science), Pharma Professional seeking career in regulatory affairs

Career Support & Placement Assistance

Along with comprehensive Regulatory Affairs training, ERA provides complete career support to help students confidently begin their professional journey in the pharmaceutical industry.

Resume Writing

Create a professional industry-standard resume.

Mock Interviews

Interview preparation with industry experts.

Placement Assistance

Career guidance and job assistance for students.

What You Will Learn

Introduction to Pharmaceutical Regulatory Affairs
Drug Development & Regulatory Framework
CTD & ACTD Dossier Preparation
Drug Master File (DMF) Documentation
Product Registration Procedures
Global Regulatory Guidelines
Regulatory Compliance Requirements
Industry Documentation Practices
Practical CTD Compilation Exercises
Career Guidance & Interview Preparation