Full Acts and Rules related to Drugs, Cosmetics, Medical Devices, other pharmaceutical Products etc
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Full Acts and Rules related to Drugs, Cosmetics, Medical Devices, other pharmaceutical Products etc
Post by QualisBioMed »
You can access full Acts and Rules related to Drugs, Cosmetics, Medical Devices, other pharmaceutical Products etc. on https://actsandrules.qualisbiomed.com/
Qualis BioMed (Admin)
Jump to
- General
- ↳ Welcome
- ↳ Announcements
- Acts & Rules
- ↳ Acts
- ↳ Drugs & Cosmetics Act, 1940
- ↳ Narcotic Drugs & Psychotropic Substances Act, 1985
- ↳ The Drugs & Magic Remedies (Objectionable Advertisement) Act, 1954
- ↳ THE CODE OF CRIMINAL PROCEDURE, 1973 ACT NO. 2 OF 1974
- ↳ Rules
- ↳ Drugs & Cosmetics Rules, 1945
- ↳ Medical Devices Rules, 2017
- ↳ New Drugs & Clinical Trials Rules, 2019
- ↳ Cosmetics Rules, 2020
- ↳ Narcotic Drugs & Psychotropic Substances Rules, 1985
- ↳ The Drugs & Magic Remedies (Objectionable Advertisement) Act, 1955
- ↳ Drugs (Prices Control) Order, 1995
- ↳ Gazette Notifications
- Pharmaceuticals
- ↳ Drugs
- ↳ Investigational New Drugs (IND) and New Drugs
- ↳ Subsequent New Drugs (SND)
- ↳ Fixed Dose Combinations (FDC)
- ↳ Biological Products
- ↳ Vaccines
- ↳ Phytopharmaceuticals
- ↳ Dosage Form
- ↳ Tablet
- ↳ Capsule
- ↳ Injection
- ↳ Pre-clinical Studies
- ↳ Clinical Studies
- ↳ Drugs Discovery
- ↳ Pharmaceutical Technology
- ↳ Quality Control
- ↳ Quality Assurance
- ↳ Quality Management System (QMS)
- ↳ Validation
- ↳ Clinical Trials
- ↳ Audits
- ↳ cGMP
- ↳ Water System
- ↳ Aseptic Processing
- ↳ SOPs
- ↳ GLP
- ↳ Stability Studies
- ↳ Instrument Calibration
- ↳ Production Facility
- ↳ Regulatory Approvals
- In-Vitro Diagnostics (IVD)
- ↳ In-Vitro Diagnostics
- ↳ In-Vitro Diagnostics (IVD) Classifications
- ↳ Quality Management System (QMS)
- ↳ Clinical Performance Study
- ↳ Quality Control
- ↳ Quality Assurance
- ↳ Engineering Design
- ↳ Software Validation
- ↳ Regulatory Approvals
- Medical Devices
- ↳ Medical Devices
- ↳ Medical Devices Classifications
- ↳ Quality Management System (QMS)
- ↳ Clinical Evaluation Reports
- ↳ Quality Control
- ↳ Quality Assurance
- ↳ Engineering Design
- ↳ Software Validation
- ↳ Regulatory Approval
- Cosmetics
- ↳ Cosmetics
- ↳ Regulatory Approval
- ↳ Manufacturing of Cosmetics
- ↳ Export / Import of Cosmetics
- ↳ Pre-Clinical Studies
- ↳ Clinical Studies
- Regulatory Updates from various National Regulatory Authorities
- ↳ Updates in Acts & Rules
- ↳ Draft Notifications
- National Regulatory Authorities (NRA)
- ↳ List of National Regulatory Authorities and their Role Healthcare
- ↳ List of Non-Statutory Agencies and their Role in HealthCare
- Intellectual Property Rights (IPR)
- ↳ Intellectual Property Rights
- ↳ Intellectual Property Rights classification
- ↳ Patent
- ↳ Miscellaneous
- Medical Products Guidelines from various Agencies
- ↳ World Health Organisation (WHO)
- ↳ International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
- Pharmacopoeia
- ↳ USP (United States Pharmacopeia )
- ↳ IP (Indian Pharmacopoeia )
- ↳ JP (Japanese Pharmacopoeia )
- ↳ EP (European Pharmacopoeia )
- ↳ Comparative topics across various Pharmacopoeia
- World Trade Organization (WTO)
- ↳ World Trade Organization and its role in the world economy
- ↳ Various treaties under WTO
- Artificial Intelligence and way ahead
- ↳ Artificial Intelligence
- ↳ Artificial Intelligence in Medical Products ( diagnostics and treatments)
- ↳ Challenges in Artificial Intelligence
- ↳ Products specific Artificial Intelligence (Case Studies)