Regulatory Compliance
Understand complex Indian and international pharma regulations in simple language and apply them correctly in your studies, projects, or business.
Who this is for
- Students preparing for exams, vivas, or projects on Drug & Cosmetics Act and related laws.
- Faculty and researchers needing regulatory clarity for research or publications.
- Small pharma businesses, retailers, or startups needing compliance guidance.
What you get
- Indian Regulatory Acts overview: Clear explanation of Drugs & Cosmetics Act, rules, schedules, licences, and authorities with easy‑to‑remember frameworks.
- International guidelines simplified: Introduction to USFDA, EMA, ICH, WHO guidelines, GMP, GLP, GCP in a beginner‑friendly way.
- Compliance strategy session: For businesses and startups—what licences are required, documentation basics, inspection preparedness, and risk areas.
- Exam and viva support: Focused sessions on important sections, likely questions, and how to write scoring answers.
How it works
- Choose “Student/Fresher” or “Business/Professional” track.
- Share your syllabus, project, or business details.
- Join a 60‑minute live session with Q&A, followed by summary notes.
Outcomes
- Strong conceptual understanding instead of rote memorisation.
- Better exam performance and viva confidence.
- Reduced regulatory risk for small businesses and entrepreneurs.
