Results 1 - 4 of
4
Most Recent Blog Posts
-
Drug Administration Law of the Drug Administration Law of the People's Republic of China
- From: grandedirector
-
Description:
http://eng.sfda.gov.cn/cmsweb/webportal/W45649037/A48335975.html
- Blog post
- 1 year ago
- Views: 70
- Not yet rated
-
FDA CDER Databases FDA CDER Databases
- From: pedrooshka
-
Description:
Databases on the CDER Website
- Acronyms and Abbreviations about the database
- Adverse Event Reporting System (AERS) about the database
- Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) about the database
- Bioresearch Monitoring Information System (BMIS) about the database
- Clinical Investigator Inspection List (CLIIL) about the database
- Dissolution Methods Database about the database
- Drug Firm Annual Registration Status about the database
- Drugs@FDA about the database
- FDA Acronyms and Abbreviations about the database
- Inactive Ingredient Search for Approved Drug Products about the database
- National Drug Code Directory about the database
- Oncology Tools about the database
- Orange Book (Approved Drug Products with Therapeutic Equivalence Evaluations) about the database
- Postmarketing Study Commitments about the database
- Blog post
- 1 year ago
- Views: 90
- Not yet rated
-
Pharmaceutical Data Bases Pharmaceutical Data Bases
- From: viernescasual
-
Description:Database Resources
These databases contain a large amount of information targeted towards the pharmaceutical industry covering a wide range of topics. Upon review of the complete list, you will be able to search for the desired topics in appropriate individual databases.
PubMed Central
Inactive Ingredient DatabaseNational Institute of Health (NIH) Search the Studies
PubMed Central Free Journal Articles
PubChem Compound Small Molecule Chemical Structures
Drug, supplement, and herbal Information
FDA Approved Animal Drug Products
Vaccine Adverse Event Reporting System
Drug Firms Annual Registration Status
- Blog post
- 1 year ago
- Views: 75
- Not yet rated
-
Global Pharmaceutical Regulato Global Pharmaceutical Regulatory Organizations
- From: pedrooshka
-
Description:
Global Organisations (supranational)
- Anatomical Therapeutic Chemical (ATC) classification and Defined Daily Dose (DDD)
- Global Harmonization Task Force (GHTF)
- IFPMA (International Federation of Pharmaceutical Manufacturers Associations)
- IFPMA Clinical Trials Portal
- International Conference on Harmonisation (ICH)
- OECD's Work on Good Laboratory Practice (GLP) and Compliance Monitoring
- The World Intellectual Property Organization (WIPO)
- World Health Organisation (WHO)
Sources of Global Regulatory Information
- CTD Guidelines
- Drug Information Association (DIA)
- reg123.com
- RegSource.com
- RegulatoryWorld (networking for regulatory professionals)
- TOPRA (The Organisation for Professionals in Regulatory Affairs)
USA
US Goverment Bodies
- CBER (FDA) Home Page
- CBER (FDA) What's New
- CDER (FDA) Home Page
- CDER (FDA) What's New
- Code of Federal Regulations (CFR)
- Drugs@FDA
- FDA Guidance Documents
- FDA's Oncology Tools
- Information for FDA-Regulated Industry
- New and Generic Drug Approvals (CDER)
- US Department of Health
- US Government Printing Office
- US Patent and Trademark Office
US Organisations
- American Association of Pharmaceutical Scientists
- Regulatory Affairs Professionals Society (RAPS)
- The Pharmaceutical Research and Manufacturers of America (PhRMA)
Europe
Europe
- European Clinical Trials Directive
- European national agencies
- European organisations
- European regulatory and government bodies
other information
Asia
- China - State Food and Drug Administration
- Hong Kong - Pharmaceutical Service, Department of Health
- India - Central Drugs Standard Control Organization
- India - Ministry of Health & Family Welfare
- Korea Food & Drug Administration
- Malaysia - National Pharmaceutical Control Bureau
- Philippine Council for Health Research and Development
- Philippines - Bureau of Food and Drugs
- Singapore - Health Sciences Authority
- Taiwan - Center fro Drug Evaluation
- Taiwan - Department of Health
- Thailand - Food & Drug Administration
Australia and New Zealand
- Australia's Therapeutic Goods Administration (TGA)
- Australian Department of Health and Ageing
- Australian Drug Evaluation Committee (ADEC)
- Australian drugs designated as orphan drugs
- New Zealand Medicines and Medical Devices Safety Authority
- New Zealand Ministry of Health
- Public Access to ARTG Medicines Information
Canada
- Canadian Society for Pharmaceutical Sciences
- Health Canada - Drug Products
- Health Canada - Medical Devices
- Health Canada - Natural Health Products
- Health Canada Online
- Public Health Agency of Canada
Central and South America
- Argentina - National Administration of Drugs, Food & Medical Technology
- Brazil - Ministry of Health
- Chile - Ministry of Health
- Mexico - Ministry of Health
Middle East
- Israel - Ministry of Health
- Morocco - Ministry of Health
- Turkey - Ministry of Health
- United Arab Emirates
Other sites
Biological and Medical
- British Medical Journal
- British National Formulary
- electronic Medicines Compendium (eMC)
- Hardin MD (Hardin Meta Directory)
- Health, Environment & Work
- healthfinder® (USA)
- Intute: Health and Life Sciences
- Medi-Lexicon
- Medical Abbreviations Search
- Medical Abbreviations Search via reg-info.com
- Medline (PubMed)
- Merck Manual
- Multilingual Glossary of medical terms
- Neuroscience for Kids
- NHS Direct
- NHS National Electronic Library for Health
- The Lancet
- The Pharmaceutical Journal
General Science
- Blog post
- 1 year ago
- Views: 73
- Not yet rated
Results 1 - 4 of
4