Module 18 | Slide 1 of 12 January 2006 GMP Inspection Process Preparation for the Inspection.

Slides:



Advertisements
Similar presentations
Basic Principles of GMP
Advertisements

The Microsoft IT Academy Quality Process. v3.0 June 2004 The key components of the Quality Programme A Quality relationship Self assessment Site visits.
COMPANY MAINTENANCE MANUAL
© WHO – PSM Validations – part 1 Workshop on GMP and Quality Assurance of TB products Kuala Lumpur Malaysia, 21 – 25 February 2005 Maija Hietava M.Sci.Pharm.
WHO - PSM Basic Principles of GMP Documentation - Part 1 Workshop on GMP and Quality Assurance of HIV products Shanghai, China 28 Feb - 4 March 2005 Maija.
Regulatory Auditing. Audit Areas Management Responsibility Auditing (internal and external) Design Control Document Control Purchasing Control Identification.
TARGETS 1.Ensure the Control of the Risk Factors for the health of the consumers based in the Mercosur harmonized legislation and norms; 2.Definition.
Annual Product Review (APR) Product Quality Review (PQR)
Module 6 | Slide 1 of Contract Production, Analysis and other activities Section 7 Basic Principles of GMP.
GMP Document and Record Retention
World Health Organization
Module 6 | Slide 1 of 14 January 2006 Contract Production and Analysis Section 7 Basic Principles of GMP.
Module 12 – part 2 | Slide 1 of 35 January 2006 Basic Principles of GMP Documentation Part 2 15.
IPC meeting June 2014 Dr Joelle DAVIAUD, Quality Assurance Specialist Model Quality Assurance System for procurement agencies.
World Health Organization
WHO GMP Certification Scheme
1 GMP Inspection Process Introduction. 2 Programme Objectives 1.Familiarise with GMP inspection 2.How to perform an inspection 3.Developing an action.
Project co-financed by European Union Project co- financed by Asean EUROPEAN COMMITTEE FOR STANDARDISATION - Implementing Agency 1 HOW TO CONDUCT AN INSPECTION.
Establish Documentation and Record Keeping (Task 12 / Principle 7)
Module 5 | Slide 1 of 22 January 2006 Sections 5 and 6 Basic Principles of GMP Complaints and Recalls.
Module 12 – part 1 | Slide 1 of 20 January 2006 Basic Principles of GMP Documentation Part 1 15.
Module 1, Part 1: Introduction and The VMP Slide 1 of 22 © WHO – EDM Validation Supplementary Training Modules on Good Manufacturing Practices.
Huzairy Hassan School of Bioprocess Engineering UniMAP.
Seafood HACCP Alliance for Training and Education Chapter 10 Principle 6: Establish Verification Procedures.
World Health Organization
Basic Principles of GMP
Basic Principles of GMP
New Zealand Medicines and Medical Devices Safety Authority A business unit of the Ministry of Health.
Module 5Slide 1 of 24 WHO - EDM Part One, Sections 6 and 7 Basic Principles of GMP Complaints and Recalls.
Project co-financed by European Union Project co- financed by Asean European Committee for Standardization Implementing Agency 1 Module 13 GMP Workshop.
Organization and Implementation of a National Regulatory Program for the Control of Radiation Sources Staffing and Training.
WHO COURSE FOR THE CARs MONITORING AND AUDITING OF FOOD LAW COMPLIANCE AND ENFORCEMENT.
Module 5 | Slide 1 of Sections 5 and 6 Basic Principles of GMP Complaints and Recalls.
Module 20 | Slide 1 of 35 January 2006 GMP Inspection Process The Inspection.
World Health Organization
Module 1Slide 1 of 16 WHO - EDM Introduction to the Training Course Basic Principles of GMP.
UNEP-GEF DEMONSTRATION PROJECTS ON IMPLEMENTATION OF NATIONAL BIOSAFETY FRAMEWORKS Arhus GMO Working Group 24 March 2004.
Module 8 | Slide 1 0f Personnel Basic Principles of GMP 9.
Organization and Implementation of a National Regulatory Program for the Control of Radiation Sources Inspection Part II.
Important informations
Module 6 | Slide 1 of Contract Production and Analysis Section 7 Basic Principles of GMP.
Paul Hardiman and Rob Brown SMMT IF Planning and organising an audit.
Module 19 | Slide 1 of 14 January 2006 GMP Inspection Process Types of GMP Inspection.
Basic Principles of GMP
30/02/2008 Dept. of Pharmaceutics 1 Salient Features of Quality Assurance Dr. Basavaraj K. Nanjwade M.Pharm., Ph.D Associate Professor Department of Pharmaceutics.
Organization and Implementation of a National Regulatory Program for the Control of Radiation Sources Inspection Part III.
A QUALITY IMPROVEMENT TOOL
Module 2Slide 1 of 26 WHO - EDM Quality Management Basic Principles of GMP Part One.
Module 12 - part 1Slide 1 of 15 WHO - EDM Basic Principles of GMP Documentation Part 1 Part One, 14.
Module 14Slide 1 of 23 WHO - EDM Basic Principles of GMP Active Pharmaceutical Ingredients Part Three, 18.
Module 12 - part 2Slide 1 of 23 WHO - EDM Basic Principles of GMP Documentation Part 2 Part One, 14.
1 CHALLENGES IN REGULATING QUALITY AND RATIONAL USE OF ANTIBIOTICS ALLIANCE FOR THE PRUDENT USE OF ANTIBIOTICS: INAGURAL MEETING COURTYARD.
CM&C Inspections The Pre-Approval Inspection (PAI) in the US 27 May 2010.
ISO 14001:2004 Clause 4.3 Planning. Clause 4.3 Planning Key Requirements of Environmental Management System Certification.
Module 7 | Slide 1 of Self-Inspection and quality audits Basic Principles of GMP.
World Health Organization
CONDUCTING OF GMP INSPECTION
PREPARATION FOR GMP INSPECTION
Company Registration: Procedure that one needs to follow Company Registration: Procedure that one needs to follow
The WHO Prequalification of Medicines Programme Capacity building agenda Dr Milan Smid.
GMP Inspection Process
GMP Inspection Process
World Health Organization
MARKETING, PURCHASING AND PRODUCTION (7 - 9%)
GMP Inspection Process
GMP Inspection Process
World Health Organization
World Health Organization
Radiopharmaceutical Production
Compliance Manual Update Staff Requirements Check
Presentation transcript:

Module 18 | Slide 1 of 12 January 2006 GMP Inspection Process Preparation for the Inspection

Module 18 | Slide 2 of 12 January 2006 Preparation for an Inspection Objectives 1. To review the activities in preparation for an inspection 2. To discuss key issues relating to preparing for inspections in this country

Module 18 | Slide 3 of 12 January 2006 Preparation for an Inspection Scope of Inspection Objective Type Depth Timing Inspectors: äsize of team ämake-up of team

Module 18 | Slide 4 of 12 January 2006 Preparation for an Inspection Notification The company being inspected Team members äexpert support äother inspectors Other interested parties

Module 18 | Slide 5 of 12 January 2006 Preparation for an Inspection Review documentation from regulatory authority Company file Site Master File Manufacturing licence Registration dossiers

Module 18 | Slide 6 of 12 January 2006 Preparation for an Inspection Review documentation from regulatory authority (continued) Reports äAdverse Drug Reaction reports (ADRs) äPrevious inspections Records äComplaints and recalls äRegulatory test results (surveillance)

Module 18 | Slide 7 of 12 January 2006 Preparation for an Inspection Review documentation from the manufacturer Annual report Complaints file Self inspection/internal audit reports Send a questionnaire to the manufacturer asking to provide specific information about the company Layout of site and diagrams Manuals Standard Operating Procedures

Module 18 | Slide 8 of 12 January 2006 Preparation for an Inspection Programme Checklist Aide-memoire for inspection Develop inspection programme Distribute inspection programme äCompany äTeam

Module 18 | Slide 9 of 12 January 2006 Preparation for an Inspection Group Session You will be given a situation that requires an inspection Prepare a list of documents that you would use in preparation for the inspection Prepare a checklist or aide-memoire of key issues to be investigated Draft a programme for the inspection

Module 18 | Slide 10 of 12 January 2006 Preparation for an Inspection Possible Issues – I The first inspection of a new manufacturer Plant design and equipment Processes Documentation Personnel Quality control

Module 18 | Slide 11 of 12 January 2006 Preparation for an Inspection Possible Issues – II Regular inspection of an established manufacturer Actions arising from the previous inspection Areas not previously inspected New areas, processes and products

Module 18 | Slide 12 of 12 January 2006 Preparation for an Inspection Possible Issues – III Inspection because of complaints about a product The product in question Manufacturing process Premises Systems for handling complaints and recalls Quality control records