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Textbook Of Regulatory Aspects Of Drugs & Cosmetics
₹499.00
This course is designed to impart the fundamental knowledge on the drug development process, regulatory
requirements for approval of new drugs, drug products and cosmetics in regulated and semi-regulated
countries. It prepares the students to learn in detail on the regulatory requirements, documentation
requirements, and registration procedures for marketing the drug products and cosmetics in regulated and
semi-regulated countries.
Textbook Of Regulatory Aspects Of Drugs & Cosmetics
₹499.00
This course is designed to impart the fundamental knowledge on the drug development process, regulatory
requirements for approval of new drugs, drug products and cosmetics in regulated and semi-regulated
countries. It prepares the students to learn in detail on the regulatory requirements, documentation
requirements, and registration procedures for marketing the drug products and cosmetics in regulated and
semi-regulated countries.
TEXTBOOK OF REGULATORY ASPECTS OF MEDICAL DEVICES
₹499.00
This Textbook is designed to impart the fundamental knowledge on the medical devices and in
vitro diagnostics, basis of classification and product life cycle of medical devices, regulatory
requirements for approval of medical devices in regulated countries like USFDA, EMA and
ASAIN countries along with WHO regulations. It prepares the students to learn in detail on the
harmonization initiatives, quality and ethical considerations, regulatory and documentation
requirements for marketing medical devices and IVDs in regulated country and global level.
TEXTBOOK OF REGULATORY ASPECTS OF MEDICAL DEVICES
₹499.00
This Textbook is designed to impart the fundamental knowledge on the medical devices and in
vitro diagnostics, basis of classification and product life cycle of medical devices, regulatory
requirements for approval of medical devices in regulated countries like USFDA, EMA and
ASAIN countries along with WHO regulations. It prepares the students to learn in detail on the
harmonization initiatives, quality and ethical considerations, regulatory and documentation
requirements for marketing medical devices and IVDs in regulated country and global level.
