Good automated manufacturing practice

Results: 12



#Item
1Press Release  IADSA releases first ever global GMP guide Australia  23 June 2011

Press Release IADSA releases first ever global GMP guide Australia 23 June 2011

Add to Reading List

Source URL: www.iadsa.org

Language: English - Date: 2011-06-23 02:56:51
2Pharma  Electronic Signatures and Audit Trail FDA 21 CFR Part II Compliant  The Industry Standard System for

Pharma Electronic Signatures and Audit Trail FDA 21 CFR Part II Compliant The Industry Standard System for

Add to Reading List

Source URL: www.iccs-ltd.co.uk

Language: English - Date: 2014-11-19 10:20:43
3Validation of New Pharmaceutical APCS Is in the Bag The Need: Part 11 Compliant Validation of an Automated Process Control System Pharmaceutical companies must validate quality-affecting computerized systems in accordanc

Validation of New Pharmaceutical APCS Is in the Bag The Need: Part 11 Compliant Validation of an Automated Process Control System Pharmaceutical companies must validate quality-affecting computerized systems in accordanc

Add to Reading List

Source URL: www.deatonengineering.com

Language: English - Date: 2009-11-10 14:25:23
4Pharmaceutical Engineering Deaton Engineering Understands Good Manufacturing Practices (GMP) The impact of long product development cycles, global competition, and current Good Manufacturing Practices presents a unique c

Pharmaceutical Engineering Deaton Engineering Understands Good Manufacturing Practices (GMP) The impact of long product development cycles, global competition, and current Good Manufacturing Practices presents a unique c

Add to Reading List

Source URL: www.deatonengineering.com

Language: English - Date: 2009-11-10 14:25:45
5Validation Engineering & FDA Compliance Specification Development, Design, Verification, and Validation of Pharmaceutical, Biopharmaceutical, Medical Device, and other FDA Regulated Industries A good validation program c

Validation Engineering & FDA Compliance Specification Development, Design, Verification, and Validation of Pharmaceutical, Biopharmaceutical, Medical Device, and other FDA Regulated Industries A good validation program c

Add to Reading List

Source URL: www.deatonengineering.com

Language: English - Date: 2009-11-10 14:28:18
6Microsoft Word[removed]Interrupted Supply - Inter-Association Summary-final report.doc

Microsoft Word[removed]Interrupted Supply - Inter-Association Summary-final report.doc

Add to Reading List

Source URL: www.efpia.eu

Language: English - Date: 2015-01-20 07:15:59
7Position:  Process Engineer Reports To:  Lead Engineer, CAPEX projects

Position: Process Engineer Reports To: Lead Engineer, CAPEX projects

Add to Reading List

Source URL: www.therapurebio.com

Language: English - Date: 2014-11-28 08:50:12
8Position:  Effective Date: Technical Support Specialist Level 1/2 Reports To:

Position: Effective Date: Technical Support Specialist Level 1/2 Reports To:

Add to Reading List

Source URL: www.therapurebio.com

Language: English - Date: 2014-12-19 16:54:41
9© World Health Organization WHO Technical Report Series, No. 908, 2003 Annex 6 Guidance on Good Manufacturing Practices (GMP): inspection report

© World Health Organization WHO Technical Report Series, No. 908, 2003 Annex 6 Guidance on Good Manufacturing Practices (GMP): inspection report

Add to Reading List

Source URL: apps.who.int

Language: English - Date: 2009-10-20 08:38:30
10Microsoft Word - PI[removed]Recommendation on Computerised Systems.doc

Microsoft Word - PI[removed]Recommendation on Computerised Systems.doc

Add to Reading List

Source URL: www.picscheme.org

Language: English - Date: 2012-06-04 15:30:40