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Pharmaceutical Administration and Regulations in Japan

Pharmaceutical Good Manufacturing Practice Guidelines of Japan.
2018-05-27T08:41:38Z PrintOnline CoursesQuestion Forum No comments
✔ Technical Review by: | Last Verified:2018-05-27T08:41:38Z

Pharmaceutical Administration and Regulations in Japan

Front cover / Contents
CHAPTER 1. ORGANIZATION AND FUNCTION OF THE MINISTRY OF HEALTH, LABOUR AND WELFARE
CHAPTER 2. PHARMACEUTICAL LAWS AND REGULATIONS
CHAPTER 3. DRUG DEVELOPMENT
CHAPTER 4. POST-MARKETING SURVEILLANCE OF DRUGS
CHAPTER 5. SUPPLY AND DISSEMINATION OF DRUG INFORMATION
CHAPTER 6. HEALTH INSURANCE PROGRAMS AND DRUG PRICING IN JAPAN
Index




 is a prominent Pharmaceutical Quality Assurance expert, consultant and the founder of Pharmaguideline. With over 22 years of hands-on experience in cGMP-compliant manufacturing environments, he specializes in establishing validation protocols, sterile area controls and data integrity systems. Ankur routinely interprets international regulatory frameworks (including FDA, EMA and ICH guidelines) to help global pharmaceutical professionals ensure strict regulatory compliance and operational excellence. Connect with Ankur on LinkedIn. Need Help: Ask Question

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