Click on the following drop down menu for some useful information
- 06 Pharma Computing Guidance & Regulatory LinksPharma Links
- 01 MHRA MHRA
- 02 GLP Guidance on ArchivingMHRA
- 03 'the 'Orange Guide' (MHRA)Orange Guide
- 04 Irish Medicines BoardIrish Medicines Board
- 05 ICH Pharmaceutical Development Q8ICH Q8
- 06 ICH Quality Risk Management Q9 ICH Q9
- 07 ICH Pharmaceutical Quality System Q10ICH Q10
- 09 European Medicines AuthorityEMA
- 10 European Union Legislation - EudralexEudralex
- 11 GMP: Annex 11, Computerised SystemsEudraLex
- 12 Application of the priciples of GLP to computerised systemsOECD
- 13 Principles of GLP and compliance monitoringOECD
- 14 Annex III to procedure for conducting GCP inspectionsEMEA
- 15 Computerised Systems used in Clinical InvestigationsFDA
- 16 CFR - Code of Federal Regulations Title 21FDA
- 17 Guidance: General Principals of Software ValidationFDA
- 18 Guidance: Quality Systems Approach to cGMP RegulationsFDA
- 19 GLP Guidelines for Spreadsheets AGIT
- 07 EmpowermentQE ResourcesOur Resources
- 08 Technical ResourcesTechnical Resources
- 01 Elements of Software ConstructionSoftware Engineering
- 02 Database SystemsDatabase
- 03 SQL IntroductionDatabase
- 04 SQL Quick RefDatabase
- 05 Database Quick TutorialDatabase
- 06 Oracle 11g R2 Documentation LibraryOracle Documentation
- 07 MySQL HomepageMySQL Homepage
- 08 Eclipse Eclipse Open Source
- 09 Soapui SoapUI Web Test
- 10 SQL Developer SQL Developer
- 11 Java VisualVM DocumentationJava VisualVM Documentation
- 12 Java VisualVMJava VisualVM