UNICEF Quality Assurance in the procurement of medicines

Similar documents
UNICEF Quality Assurance in the procurement of medicines

UNICEF s Quality Assurance System for Procurement of Finished Pharmaceutical Products

UNICEF Requirements for RUTF Manufacturers

Contents. 1. Certification of Materials 2. Supply of Materials

New GMPs for Active Substances & Excipients. Presented by Eoin Hanley 4 July, 2016

Session 4: Ensuring Product Quality Throughout the Supply Chain

Session 1: Prequalification and Procurement

GMP GUIDELINES. GMP Guides from Industry Organisations. FDA cgmp WHO GMP. cgmp Guide Drugs 21 CFR 210 GAMP. ISPE Technical Guides

QUESTIONNAIRE FOR COMPETENT AUTHORITIES TO BE USED FOR ASSESSMENT, REASSESSMENT AND SELF- EVALUATION

Pharmaceutical product technical requirements and the Interagency pharmaceutical product questionnaire

Model Quality Assurance System for procurement agencies. What it means for manufacturers?

EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL. EudraLex The Rules Governing Medicinal Products in the European Union

GMP Inspection Process. Types of GMP Inspection. Module 18 Slide 1 of 14 WHO - EDM

INVESTING IN CHILDREN

Data Collection Tools Functions, Indicators & Sub-Indicators

Guidelines for the international procurement of vaccines and sera

EUROPEAN INDUSTRIAL PHARMACISTS GROUP. Guidance on CPD for QUALIFIED PERSONS

GUIDELINES ON THE PRINCIPLES OF GOOD DISTRIBUTION PRACTICE OF ACTIVE SUBSTANCES FOR MEDICINAL PRODUCTS FOR HUMAN USE

Revised Global Fund Quality Assurance Policy for Pharmaceutical Products and Price &Quality Reporting

What we do. UNICEF Supply Division s work is a direct input to development programmes and emergency response

Applying a Knowledge-Based Approach to Pharmaceutical Supply Chain Temperature Control Management

2012 Joint Guideline Launch

Cold Chain Committee Guidance for shippers, transport service providers and subcontractors

Control of veterinary products and vaccines Inspection system, monitoring plan, monitoring of vaccines distribution

Phase Appropriate GMPs for IMPs. Presented by: Karen S. Ginsbury For: IFF, October 31, Nov 02, 2017

Session 13: Prequalification Within the Context of Global Fund Procurements

PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME. PI July 2018

Quality assurance for essential medicines and health products. IPC meeting: December 2012

Session 5: Increase in Use of the WHO Prequalification Programme

Good Procurement Practices for artemisinin-based antimalarial medicines

European Union (EU) Regulatory Trends in GMP. Clive Brading Tianjin, China September 23, 2009

Overview of Regulatory Requirements for API and Formulations

UNICEF TECHNICAL REQUIREMENTS FOR MEDICAL DEVICES (MD)

Introduction of new suppliers to UNICEF procurement mechanisms

Wholesaling & Distribution & the GMPs

Wholesaling & Distribution & the GMPs

V. S. International Pvt. Ltd

Prequalification Team WHO PUBLIC INSPECTION REPORT Vaccine Manufacturer

MANUFACTURE OF INVESTIGATIONAL MEDICINAL PRODUCTS

Oursourcing and Supplier Qualification from the perspective of the pharmaceutical Industry

Procurement Capacity Toolkit

GLOBAL HEALTH SUPPLY CHAIN QUALITY ASSURANCE

GMP Compliance. George Acevedo, CQV Senior Engineer M+W Singapore Pte. Ltd

GLOBAL HEALTH SUPPLY CHAIN QUALITY ASSURANCE QA.APP.GEN-52 Laboratory Commodities and Consumables: Supplier Technical Questionnaire

On Approval of the Rules on Importation and Exportation of Medicines, Products of Medical Purposes and Medical Equipment

GUIDE TO GOOD MANUFACTURING PRACTICE FOR MEDICINAL PRODUCTS

Inspection of API Manufacturers & Update on Registration Process

Management System Hilton Olympia, London 13 th February 2013

White paper: Code of GMP Chapter 4 Documentation - PIC/S versus EU

Supplier questionnaire. 1. Organisation Details (Mandatory) Quality Department Details (or representative)

Webinar Expert Module 3: GMP Inspections Dupont

INTERCOUNTRY COOPERATION IN SUPPLY OF ESSENTIAL DRUGS

Prequalification of Medicines Programme. WHO PUBLIC INSPECTION REPORT (WHOPIR) API Manufacturer

UNICEF Supply Division Copenhagen. Quality Assurance

Vendor Qualification Survey

Supplier Quality Survey

SUPPLIERS QUALIFICATION

CLICK TO ADD TITLE [SPEAKERS NAMES]

Quality Quality problems r API used used in essent essen ial t ial medicines : Role e of of WHO and and its its pre pr lifi qua ca i ttion on progr

NQA-1 Graded Approach, 55-Gallon Drum Summary

Good Distribution Practice and Supply Chain Risk Evaluation

UNICEF s Procurement Processes and Tendering for Diagnostics

Training manual: licensing, lot release, laboratory access

Prequalification of Medicines Programme

Annex 4. Assessment tool based on the model quality assurance system for procurement agencies: aide memoire for inspection

Issues related to procurement of nutrition products

SITE MASTER FILE For MHRA

Drug Quality Assurance: Systems at ChemCon Author: Dr. Peter Gockel

18.H Questionnaire for preparing GMP-inspections

DJ Cockburn Head of Manufacturing and Quality Compliance European Medicines Agency

Contents. Contents (13) 1 Production (23)

Documenta tion and Records

Development of contract manufacturing on the example PJSC «Pharmimex»

SUPPLIER QUALITY REQUIREMENTS

Validation Requirements for Nutrition Products

Supplier Assurance Program. CBE Pty Ltd

Supersedes Division Name Revision No. 0 Export Division Page No. 1 of 9

Session 2: Overview of the WHO Prequalification Programme for Condoms

(Information) INFORMATION FROM EUROPEAN UNION INSTITUTIONS, BODIES, OFFICES AND AGENCIES EUROPEAN COMMISSION

Waiting for Eurasian Union GMP inspection. Gap-analysis from the point of view of the Russian manufacturer

Overview SFLGDP1. Develop, implement and maintain a quality system to control the distribution of medicinal products

Procurement and Supply Management of Pharmaceuticals and other Health Products.

Quality Agreements with CMO s. Presented at ASQ Orange Empire Meeting May 13, 2014 By Luke Foo Sr. Director QA/QC Spectrum Pharmaceuticals

Working Party on Control of Medicines and Inspections. Final Version of Annex 16 to the EU Guide to Good Manufacturing Practice

Appropriate Control Strategies Eliminate the Need for Redundant Testing of Pharmaceutical Products

Quality Assurance in Pharmaceutical and Biotech Industries as Per Regulatory Guidelines

GMP Track 1 Day 2 Session 1 Vendor Assurance

ANMAT Order No 5260/2008

INFORMATION REQUIRED FROM PHARMACEUTICAL FIRMS FOR REGISRATION

PIC/S Assessment & Joint Reassessment Programme REVISED PIC/S AUDIT CHECKLIST

WHY UNITAID MATTERS FOR PEOPLE LIVING WITH HIV/AIDS, TB AND MALARIA MARKET IMPACT

ANNEX 5 PRODUCT SPECIFICATIONS AND TECHNICAL REQUIREMENTS

Feedback from Inspection Programme

Prequalification of Medicines Programme

Supplies and Reagents

EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL

Prequalification Team Inspection services WHO PUBLIC INSPECTION REPORT (WHOPIR) Finished Product Manufacturer. Tablets

Guide to Scientific and Regulatory Advice for GXP activities

Overview sulla nuova guideline GDP

Orange and Yellow Guides

Transcription:

UNICEF Quality Assurance in the procurement of medicines Peter S. Jakobsen 30 October 2006 Quality Assurance Centre SUPPLY DIVISION

Today s presentation addresses 3 questions: How is UNICEF involved in quality assurance of essential medicines What does UNICEF check before it enters into a contract with a supplier What does UNICEF check after it enters into a contract with a supplier 2

Quality Assurance cover the following tasks Receipt of Goods and GMP inspections Non-pharmaceuticals Pharmaceuticals Financial evaluation of suppliers Vendor Master / UNGM Receipt of bids / tabulation of offers Quality System 3

UNICEF s quality system is based on: Division and Centre Procedures Available electronically on the UNICEF intranet ISO 9000:2001 to be implemented 2006 2007 Quality System for GMP inspections in accordance with PIC-S Quality System requirements for GMP inspectorates WHO Model QA system for Procurement to be implemented 4

Today s presentation addresses 3 questions: Conclusion (1) UNICEF has a well established Quality Assurance System in place What does UNICEF check before we contract a supplier 5

Pre-qualification - Pharmaceuticals Suppliers Review of documentation Good Manufacturing Practice (GMP) inspections to ensure compliance with WHO GMP guidelines Products Product Questionnaire as in Model QA System WHO TRS 937 6

Pre-qualification of suppliers How? Technical questionnaire Manufacturing site Dosage forms Export experience License to manufacture pharmaceuticals Is a GMP inspection needed? 7

GMP inspections Decision based on the regulatory environment in country of origin GMP inspection by UNICEF or a representative selected by UNICEF Contract Manufacture only accepted if sub-contractor also is approved by UNICEF 8

GMP inspections by UNICEF To check compliance with WHO GMP Guidelines Primarily done by UNICEF staff 102 GMP inspections carried out in 2003-2006. 38 companies failed (37 %) Detailed GMP inspection report forwarded to company with request to respond within 1 month 9

GMP inspections collaborations Local authority invited to participate Joint inspections with WHO UNICEF is an observer to the Pharmaceutical Inspection Cooperation Scheme (PIC-S) 10

Pre-qualification of products Done in connection with Invitation to Bid (ITB) by the HIV / Health Center (HHC) Company to complete questionnaire and forward supporting documentation Supply Agreement with best offer 1-2 back-up suppliers 11

Pre-qualification of suppliers of Vaccines, HIV/AIDS, malaria and TB products Products must be pre-qualified by WHO and listed on the WHO website Supplier has confirmed to UNICEF that products are identical to those assessed by WHO/UNICEF UNICEF s purchase is traced in WHO/UNICEF GMP inspections. 12

Today s presentation addresses 3 questions: Conclusion (1): Conclusion (2): Quality Assurance has a team of professionals and a well documented quality system Quality Assurance focuses on identifying supplier and product quality before we sign the first contract What does UNICEF check after it enters into a contract with a supplier 13

QAC is performing the following activities after we contract a supplier Supply Division licensed by the Danish Medicines Agency (DMA) to wholesale pharmaceutical products to handle narcotic or psychotropic substances Compliance with European Union guidelines on Good Distribution Practice (GDP) 14

GDP ensures Quality system implemented Organisation defined Training of personnel in GDP Adequate facilities Written procedures Records of purchase and sale Self-inspections performed Recalls can be carried out 15

Products received in the warehouse are always quality inspected Visual inspection Product Dosage form and strength Quantity Certificate of analysis Satisfactory remaining shelf-life? Was it manufactured by the approved site? 16

Quality control testing Analysis performed on a random basis according to an annual plan Analysis performed by Therapeutic Goods Administration, Australia and USP, USA Collaboration with WHO on testing of HIV/AIDS products 17

Quality control of direct shipments Pre-delivery inspections - Third party - Country Office Review of packing list and Certificate of Analysis Random quality control testing in accordance with prior experience 18 18

Quality Assurance is bringing you quality products from premium suppliers Conclusion (1): Conclusion (2): Conclusion (3): Quality Assurance has a team of professionals and a well documented quality system Quality Assurance are spending many resources on securing supplier and product quality before we sign the first contract Quality Assurance closely and continuously monitors the performance of our suppliers 19