An NSF International Company EU issues draft revision of GMP Chapter 6
Monday the 22nd April 2013
The EU has issued a draft revision to Chapter 6, on Quality Control, of their GMP guide (see attached pdf where the main changes have been highlighted).
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- QP Series 13 - October 2014 to September 2016
- FDA Draft Guidance on Specification of the UFI System for Drug Establishments
- ASEAN Process Validation Draft Guidance
- Revised EU GMP Chapter 2
- Strategy for Drug-Device Combinations - Navigate the regulatory labyrinth
- Royal Pharmaceutical Society Annual Conference 2013, 8 – 9 September, Birmingham, UK
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- Letter from DG SANCO on API importation into the EU
- NSF-DBA at AFI Annual Symposium, Rimini, Italy, 2013
- USA added to EC list of approved exporting countries
- NSF DBA create interactive hand washing advice for the Pharmaceutical Industries
- India publishes list of API Written Confirmations
- Japan added to EU 'White List' for importation of APIs
- Venga a conoscere il Team di NSF Health Sciences al Simposio AFI di Rimini dal 12-14 Giugno 2013, stand 76.
- Meet the NSF Health Sciences Team at the AFI Annual Symposium in Rimini, Italy from 12-14 June 2013, stand 76.
- May
- April
- NSF International Acquires IPEA
- Importation of APIs into the EU
- FDA Update: Janet Woodcock CDER, at recent FDLI event in DC
- EU Upgrades its GMP Database
- EU issues draft revision of GMP Chapter 6
- EU API Import Q&A Version 4.1
- EU FMD 'Safety Features' Implementation
- Formulation and Processing (QP Module 3) - Another Great Success.
- Version 4 of the Commission Q&A on the importation of APIs from outside of the EU
- Draft SUPAC Manufacturing Equipment Addendum
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