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PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME PE 009-10 (Part II) 1 January 2013 GUIDE TO GOOD MANUFACTURING PRACTICE FOR MEDICINAL PRODUCTS…
PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME PE 009-13 (Part I) 1 January 2017 PE 009-13 (Part I) 1 January 2017 GUIDE TO GOOD MANUFACTURING…
PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME PE 009-11 (Part II) 1 March 2014 PE 009-11 (Part II) 1 March 2014 GUIDE TO GOOD MANUFACTURING…
Slide 1 PART II GOOD MANUFACTURING PRACTICES (GMP) Slide 2 GMP Prerequisite programs which will provide the basic environmental and operating conditions that are necessary…
National Validation Forum II by Trevor Schoerie Guidelines • Restrooms, safety, fire • Confidentiality – Chatham house rules • Please relax, enjoy yourself and contribute…
II ISSUE 6 SEPTEMBER 2009 MARINE NEWS THE IUCN GLOBAL MARINE PROGRAMME NEWSLETTER 2008 - 2009 GMP NEWS MARINE NEWS Issue 6, September 2009 IUCN Global Marine Programme Rue…
PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME PE 009-9 (Part I) 1 September 2009 GUIDE TO GOOD MANUFACTURING PRACTICE FOR MEDICINAL PRODUCTS…
PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME PE 009-10 (Part I) 1 January 2013 GUIDE TO GOOD MANUFACTURING PRACTICE FOR MEDICINAL PRODUCTS…
PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME PE 009-8 (Part I) 15 January 2009 GUIDE TO GOOD MANUFACTURING PRACTICE FOR MEDICINAL PRODUCTS…
Slide 1 Module 4Slide 1 of 23 WHO - EDM Validation Basic Principles of GMP Slide 2 Module 4Slide 2 of 23 WHO - EDM Validation Objectives l To review the definition and types…
V O L U M E 1 I S S U E 1 2 0 N O V E M B E R , 2 0 1 2 GliMPse Student Magazine, General Management Programme 2012 - 2013 V O L U M E 1 I S S U E 1 2 0 N O V E M B E R ,…
[SCHEDULE M] [See Rules 71, 74, 76 and 78] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS. Note: - To achieve…
Slide 1 Module 14 | Slide 1 of 19 2013 Basic Principles of GMP GMP for Sterile Pharmaceutical Products Part 2 Annex 6. TRS 961, 2011 Slide 2 Module 14 | Slide 2 of 19 2013…
GMP Inspection ProcessBasic Principles of GMP World Health Organization * * In Part 1, we discussed general aspects in the production of sterile products, requirements for
Slide 1 Module 14 | Slide 1 of 34 2013 Basic Principles of GMP GMP for Sterile Pharmaceutical Products Part 1 Annex 6. TRS 961, 2011 Slide 2 Module 14 | Slide 2 of 34 2013…
Slide 1Personnel * * Companies can make investments and buy facilities and equipment. However, the greatest resource that a company has is its personnel. But human resources
Guidance for Industry: Current Good Tissue Practice (CGTP) and Additional Requirements for Manufacturers of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)Tissues,
138 Journal of Young Pharmacists Vol 3 / No 2 contaminated and recipients developed infections. An unwritten change to autoclave operation, communicated orally between operators,…
MHRA GMP Symposium 2014 Novotel London West, London . 10 12 December 2014 Data Integrity: A new look at an old issue . . David Churchward, Expert GMP Inspector Tracy Lovatt,…
1. OOP – Back to Basic! Gøran Hansen Seniorkonsulent, Capgemini http://blog.goeran.no [email_address] Twitter.com/goeran 2. 3. 4. 5. 6. ” Vi kanunngå spagettikodeved…