Life Sciences Research to Product Development
portes grátis
Life Sciences Research to Product Development
Regulatory Requirement Transforming, Volume 1
Chattopadhyay, Pronobesh; Goyary, Danswrang
Taylor & Francis Ltd
03/2024
244
Dura
Inglês
9781032504261
15 a 20 dias
Descrição não disponível.
Chapter 1: Process of Drug Discovery
Chapter 2: History of Drug Regulatory Authorities
Chapter 3: Regulatory of Herbal and Ayurvedic Drug in the context of AYUSH and DCGI
Chapter 4: Traditional medicine (TM)- Regulatory Requirement
Chapter 5: Enforcement of Drug & Cosmetics Act, 1940 to Ayurvedic and Unani Drugs in India
Chapter 6: Ayurvedic Drugs Regulation in India
Chapter 7: Licensing procedure of Indian System of medicine (Ayurveda, Unani, Siddha and Homoeopathy Drugs)
Chapter 8: Regulatory Approval Process of Phytopharmaceuticals, Herbal Drugs or Isolated Compounds from plants or New Claim other than AYUSH Drugs
Chapter 9: Safety and toxicity of Ayurveda, Siddha and Unani (ASU) drugs
Chapter 10: The embarking of Food Safety and Standards Authority of India (FSSAI) and implantation of Food Safety and Standards Act
Chapter-11: Herbal as food vs Drugs: Regulatory framework
Chapter 12: Regulatory Approval and Commercialization process herbal as Insecticide
Chapter 13: Safety studies or pre-clinical toxicity of Modern Medicine
Chapter 14: Clinical trial procedures including the modern medicine and ayurvedic therapies
Chapter 15: Stability Testing of Drugs
Chapter 16: Regulation of Clinical Trial and Role of Institutional Human Ethical Committee
Chapter 2: History of Drug Regulatory Authorities
Chapter 3: Regulatory of Herbal and Ayurvedic Drug in the context of AYUSH and DCGI
Chapter 4: Traditional medicine (TM)- Regulatory Requirement
Chapter 5: Enforcement of Drug & Cosmetics Act, 1940 to Ayurvedic and Unani Drugs in India
Chapter 6: Ayurvedic Drugs Regulation in India
Chapter 7: Licensing procedure of Indian System of medicine (Ayurveda, Unani, Siddha and Homoeopathy Drugs)
Chapter 8: Regulatory Approval Process of Phytopharmaceuticals, Herbal Drugs or Isolated Compounds from plants or New Claim other than AYUSH Drugs
Chapter 9: Safety and toxicity of Ayurveda, Siddha and Unani (ASU) drugs
Chapter 10: The embarking of Food Safety and Standards Authority of India (FSSAI) and implantation of Food Safety and Standards Act
Chapter-11: Herbal as food vs Drugs: Regulatory framework
Chapter 12: Regulatory Approval and Commercialization process herbal as Insecticide
Chapter 13: Safety studies or pre-clinical toxicity of Modern Medicine
Chapter 14: Clinical trial procedures including the modern medicine and ayurvedic therapies
Chapter 15: Stability Testing of Drugs
Chapter 16: Regulation of Clinical Trial and Role of Institutional Human Ethical Committee
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
regulatory affairs;pharmacovigilance;toxicology studies;institutional review board;food drug interface;ayurvedic product licensing;herbal medicine regulatory compliance
Chapter 1: Process of Drug Discovery
Chapter 2: History of Drug Regulatory Authorities
Chapter 3: Regulatory of Herbal and Ayurvedic Drug in the context of AYUSH and DCGI
Chapter 4: Traditional medicine (TM)- Regulatory Requirement
Chapter 5: Enforcement of Drug & Cosmetics Act, 1940 to Ayurvedic and Unani Drugs in India
Chapter 6: Ayurvedic Drugs Regulation in India
Chapter 7: Licensing procedure of Indian System of medicine (Ayurveda, Unani, Siddha and Homoeopathy Drugs)
Chapter 8: Regulatory Approval Process of Phytopharmaceuticals, Herbal Drugs or Isolated Compounds from plants or New Claim other than AYUSH Drugs
Chapter 9: Safety and toxicity of Ayurveda, Siddha and Unani (ASU) drugs
Chapter 10: The embarking of Food Safety and Standards Authority of India (FSSAI) and implantation of Food Safety and Standards Act
Chapter-11: Herbal as food vs Drugs: Regulatory framework
Chapter 12: Regulatory Approval and Commercialization process herbal as Insecticide
Chapter 13: Safety studies or pre-clinical toxicity of Modern Medicine
Chapter 14: Clinical trial procedures including the modern medicine and ayurvedic therapies
Chapter 15: Stability Testing of Drugs
Chapter 16: Regulation of Clinical Trial and Role of Institutional Human Ethical Committee
Chapter 2: History of Drug Regulatory Authorities
Chapter 3: Regulatory of Herbal and Ayurvedic Drug in the context of AYUSH and DCGI
Chapter 4: Traditional medicine (TM)- Regulatory Requirement
Chapter 5: Enforcement of Drug & Cosmetics Act, 1940 to Ayurvedic and Unani Drugs in India
Chapter 6: Ayurvedic Drugs Regulation in India
Chapter 7: Licensing procedure of Indian System of medicine (Ayurveda, Unani, Siddha and Homoeopathy Drugs)
Chapter 8: Regulatory Approval Process of Phytopharmaceuticals, Herbal Drugs or Isolated Compounds from plants or New Claim other than AYUSH Drugs
Chapter 9: Safety and toxicity of Ayurveda, Siddha and Unani (ASU) drugs
Chapter 10: The embarking of Food Safety and Standards Authority of India (FSSAI) and implantation of Food Safety and Standards Act
Chapter-11: Herbal as food vs Drugs: Regulatory framework
Chapter 12: Regulatory Approval and Commercialization process herbal as Insecticide
Chapter 13: Safety studies or pre-clinical toxicity of Modern Medicine
Chapter 14: Clinical trial procedures including the modern medicine and ayurvedic therapies
Chapter 15: Stability Testing of Drugs
Chapter 16: Regulation of Clinical Trial and Role of Institutional Human Ethical Committee
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
