NDS Environment - A Tour of France

Size: px
Start display at page:

Download "NDS Environment - A Tour of France"

Transcription

1 FRENCH EXPERIENCE WITH NDS EIGHTH NDS USERS GROUP MEETING MEXICO 7-9 OCTOBER 2013 Aldine Fabreguettes The French National Agency for Medicines and Health Products Safety Narcotics and Psychotropics Department 0

2 CURRENT SITUATION IN FRANCE : NDS 6 March 2004 : implementation and production use of NDS 5.1 February May September 2009 : participation to the NDS user Meeting in Mexico September 2006 : Implementation and Production of NDS 6.0 October 2013 : NDS 6.0 = Current version 2011 : participation to expert group meetings on an international electronic import and export authorization system for controlled substances : the budget proposal and the provisional schedule for the installation of the new applications of the NDS Program (NDS WEB and NDS SPA) are under discussion with the general management Change of network server + update our NDS current version 1

3 CURRENT SITUATION IN FRANCE : NDS 6.0 Transactions on international level : Import/export authorizations per year Increase since Narcotic import Narcotic export Psychotropic import Psychotropic export Total

4 CURRENT SITUATION IN FRANCE : NDS 6.0 Transactions on Domestic level : Domestic licences per year Increase and stabilisation Manufacturers Wholesalers Scientific use Custom agent Total

5 CURRENT SITUATION IN FRANCE : NDS 6.0 Report : Quarterly and annual statistics : Form A, AP, B, C et P Number of laboratories : Master : Pure Substance Master = 741 Pure substance codes Substance Master = 1481 substance codes Preparation Master = 3741 préparations codes Establishment Master = 7704 establishment codes Will and need to simplify these activities - To cope with the increasing workload - To improve processing time and maintain the same control - To improve the quality of datas for statistics and the respect of the deadlines With NDS WEB and SPA Symplifying French regulation (in progress) 4

6 CURRENT SITUATION IN FRANCE : NDS 6 Possibility to make several types of requests and to export to excel : Quick and easy Quarterly and Annual statistics : Identification of non endorsed permit Inspection : To give a chronological account of domestic licences and import/export authorizations of one establishment To give a cartography of authorised establishment according to type of activities in France (manufacturer / wholesaler / raw materiel/ medicine ) Our activity report (monthly and annually) Number of domestic licenses and import/export authorizations 5

7 CURRENT SITUATION IN FRANCE : NDS 6 Developement of an additional application related to NDS : «Assistant» Recording the estimates, the current approved and endorsed quantities for each country checking of estimates before issuing a permit Developement of an electronic data exchange with the Customs = «Gun Project» Project is in progress Not limited to narcotics and psychotropics substances / for all medicines 6

8 PROJECTS NDS WEB, SPA and IIES seem to take into account the main suggested improvements proposed in 2009 electronic submissions = NDS WEB and SPA import/export authorizations = IIES checking estimate before issuing authorization Identification of import for reexport shipment Master Preparation Substances : Inactivate some preparation codes to clean up the application (3741 preparation codes) Mistakes Duplications These measures are particularly important with the implementation of NDS WEB to control the data entered by laboratories 7

9 CONCLUSION : NDS WEB / SPA and I2ES Simplification policy in French Agency +++ Data cleaning in NDS (preparation codes, establishment ) Change of network server + Update our NDS current version Implementation of NDS WEB and SPA Training of 2 pharmacists and 3 database administrators of ANSM Training of different companies Pilot phase Roll out IIES : France renew its interest in participating in the development of such a project 8

SADC GUIDELINES ON IMPORT AND EXPORT PROCEDURES FOR PHARMACEUTICAL PRODUCTS

SADC GUIDELINES ON IMPORT AND EXPORT PROCEDURES FOR PHARMACEUTICAL PRODUCTS SADC GUIDELINES ON IMPORT AND EXPORT PROCEDURES FOR PHARMACEUTICAL PRODUCTS June 2006 1 INTRODUCTION Public health concerns demand that the manufacture of pharmaceutical products and their subsequent handling

More information

OST : Procurement, Supply Chain and Service Delivery

OST : Procurement, Supply Chain and Service Delivery OST : Procurement, Supply Chain and Service Delivery Structure of the presentation International regulatory framework for narcotic / psychotropic substances Procurement procedures Supply chain mechanism

More information

UNICEF s Quality Assurance System for procurement of medicines

UNICEF s Quality Assurance System for procurement of medicines UNICEF s Quality Assurance System for procurement of medicines QA Specialist Peter Svarrer Jakobsen Joint UNICEF, UNFPA and WHO Meeting with Manufacturers and Suppliers UN City, Copenhagen 23 September

More information

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

Working Party on Control of Medicines and Inspections. Final Version of Annex 16 to the EU Guide to Good Manufacturing Practice Version 8 (final) EUROPEAN COMMISSION ENTERPRISE DIRECTORATE-GENERAL Single market, regulatory environment, industries under vertical legislation Pharmaceuticals and cosmetics Brussels, July 2001 S\common\legal-legislation\75-319nd81-851\91-356\eudralexvol4\Annex

More information

Administrative Burdens of Regulation Department of Health

Administrative Burdens of Regulation Department of Health Administrative Burdens of Regulation Department of Health 2 ADMINISTRATIVE BURDENS OF REGULATION DEPARTMENT OF HEALTH Administrative Burdens of Regulation Department of Health As part of its strategy for

More information

European Code of Conduct on Data Centre Energy Efficiency

European Code of Conduct on Data Centre Energy Efficiency EUROPEAN COMMISSION DIRECTORATE-GENERAL JRC JOINT RESEARCH CENTRE Institute for Energy Renewable Energies Unit European Code of Conduct on Data Centre Energy Efficiency Introductory guide for applicants

More information

THEME: PROMOTING GOOD PRACTICES IN DRUG POLICY DEVELOPMENT AND IMPLEMENTATION

THEME: PROMOTING GOOD PRACTICES IN DRUG POLICY DEVELOPMENT AND IMPLEMENTATION Page 1 AFRICAN UNION UNION AFRICAINE UNIÃO AFRICANA Addis Ababa, ETHIOPIA P. O. Box 3243 Telephone 251-11-5517 700 Fax 251-11-5517 844 website: www. africa-union.org 5 th SESSION OF THE AU CONFERENCE OF

More information

SC-A-063 (Ver 10-09/15) Page 3 of 6

SC-A-063 (Ver 10-09/15) Page 3 of 6 Singapore Customs, Procedures & Systems Branch 55 Newton Road, #07-01, Revenue House Singapore 307987 Contact.: 6355 2000 Fax.: 6355 2156 Email: customs_stgc@customs.gov.sg APPLICATION FOR PERMIT TO TRANSMIT

More information

THEME: PROMOTING GOOD PRACTICES IN DRUG POLICY DEVELOPMENT AND IMPLEMENTATION

THEME: PROMOTING GOOD PRACTICES IN DRUG POLICY DEVELOPMENT AND IMPLEMENTATION Page 1 AFRICAN UNION UNION AFRICAINE UNIÃO AFRICANA Addis Ababa, ETHIOPIA P. O. Box 3243 Telephone 251-11-5517 700 Fax 251-11-5517 844 website: www. africa-union.org 5 th SESSION OF THE AU CONFERENCE OF

More information

Narcotics Ordinance on Charges (Betäubungsmittel-Kostenverordnung) Introductory clause

Narcotics Ordinance on Charges (Betäubungsmittel-Kostenverordnung) Introductory clause Narcotics Ordinance on Charges (Betäubungsmittel-Kostenverordnung) (locator: BGBl. I 2009, 1675) Introductory clause On the basis of section 25 subsection 2 of the Narcotics Act (Betäubungsmittelgesetz),

More information

GMP Issues for Start-Ups, quality in the supply chain and role of the Qualified Person (QP)

GMP Issues for Start-Ups, quality in the supply chain and role of the Qualified Person (QP) GMP Issues for Start-Ups, quality in the supply chain and role of the Qualified Person (QP) Presented by: Patrick Costello Scientific Administrator, European Medicines Agency An agency of the European

More information

Guidelines for Governments on Preventing the Illegal Sale of Internationally Controlled Substances through the Internet

Guidelines for Governments on Preventing the Illegal Sale of Internationally Controlled Substances through the Internet INTERNATIONAL NARCOTICS CONTROL BOARD Guidelines for Governments on Preventing the Illegal Sale of Internationally Controlled Substances through the Internet UNITED NATIONS INTERNATIONAL NARCOTICS CONTROL

More information

European Code of Conduct on Data Centre Energy Efficiency

European Code of Conduct on Data Centre Energy Efficiency European Code of Conduct on Data Centre Energy Efficiency Introductory guide for applicants Version 1.0.0 1 of 5 1 Summary This document provides guidance notes for organisations wishing to sign the European

More information

PRIOR NOTICE OF IMPORTED FOOD SHIPMENTS A

PRIOR NOTICE OF IMPORTED FOOD SHIPMENTS A U.S. Food and Drug Administration Protecting the U.S. Food Supply U.S. Department of Health and Human Services What You Need to Know About PRIOR NOTICE OF IMPORTED FOOD SHIPMENTS A Small Entity Compliance

More information

CONSULTATION DRAFT Misuse of Drugs (Amendment) Regulations, 2013

CONSULTATION DRAFT Misuse of Drugs (Amendment) Regulations, 2013 CONSULTATION DRAFT Misuse of Drugs (Amendment) Regulations, 2013 to amend the Misuse of Drugs Regulations, 1988 as amended August 2013 INTRODUCTION What is the purpose of this consultation? The purpose

More information

Data submission of authorised medicines in the European Union

Data submission of authorised medicines in the European Union 23 February 2015 EMA/471367/2014, Rev. 1 1 Business Data and Support Department Data submission of authorised medicines in the European Union Outlines on Article 57(2) of Regulation (EC) No 726/2004 1

More information

French National Agency for Medicines and Health Products Safety (ANSM) :

French National Agency for Medicines and Health Products Safety (ANSM) : French National Agency for Medicines and Health Products Safety (ANSM) : Reinforcing the collaboration with healthcare professionals and patient associations Dany BONNET Scientific information manager

More information

LAW ON MEDICINES. Article 1. Article 2. Article 3 Manufacturing and marketing of medical devices is the activity of public interest.

LAW ON MEDICINES. Article 1. Article 2. Article 3 Manufacturing and marketing of medical devices is the activity of public interest. LAW ON MEDICINES I BASIC PROVISIONS Article 1 This Law regulates conditions for manufacturing and marketing medicines for human use and use in veterinary medicine, measures for quality assurance, safety

More information

Natural Health Products Directorate - Direction des produits de santé naturels

Natural Health Products Directorate - Direction des produits de santé naturels Site Licensing & Good Manufacturing Practices Requirements for Natural Health Products in Canada Canadian Association of Professional Regulatory Affairs Annual Education Day - June 5, 2012 Raymond W. Tsang,

More information

Implementation strategy for ISO IDMP in EU

Implementation strategy for ISO IDMP in EU Implementation strategy for ISO IDMP in EU Paolo Alcini Head of Data Standardisation and Analytics Business Data & Analytics Information Management EMA An agency of the European Union The EU ISO IDMP Task

More information

Export Import Bank Financing Programs

Export Import Bank Financing Programs Export Import Bank Financing Programs The Export Import Bank of the United States (Ex Im Bank) is the official export credit agency of the United States. Ex Im Bank assists in financing the export of U.S.

More information

Resolution 53/4. publication, Sales No. E.09.XI.1). 4 Report of the International Narcotics Control Board for 2009 (United Nations

Resolution 53/4. publication, Sales No. E.09.XI.1). 4 Report of the International Narcotics Control Board for 2009 (United Nations Resolution 53/4 Promoting adequate availability of internationally controlled licit drugs for medical and scientific purposes while preventing their diversion and abuse The Commission on Narcotic Drugs,

More information

Medical Device Regulatory Requirements for Mexico

Medical Device Regulatory Requirements for Mexico Medical Device Regulatory Requirements for Mexico Updated: June 2011 Disclaimer: The information contained in this profile is derived from public sources, is intended to assist U.S. exporters in performing

More information

The French Digital Plan for Education

The French Digital Plan for Education The French Digital Plan for Education Since December 2012, the Ministry of National Education, Higher Education and Research has been developing an ambitious strategy to bring schools into the digital

More information

APPROVE A BUDGET THAT WOULD ALLOW FULL IMPLEMENTATION OF THE NATIONAL ANTI- DRUG PLAN PUBLICATION DATE: JANUARY 2003

APPROVE A BUDGET THAT WOULD ALLOW FULL IMPLEMENTATION OF THE NATIONAL ANTI- DRUG PLAN PUBLICATION DATE: JANUARY 2003 RECOMMENDATION 1: APPROVE A BUDGET THAT WOULD ALLOW FULL IMPLEMENTATION OF THE NATIONAL ANTI- DRUG PLAN Nicaragua reports that it negotiated a loan with the Inter-American Development Bank (IDB), to be

More information

EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL

EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Ref. Ares(2011)1044649-03/10/2011 EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Pharmaceuticals SANCO/D3/RSR/iv(2011)ddg1.d3. 1137738 Update 1 October 2011 HANDLING

More information

Client Time Analysis Dashboard Users Guide

Client Time Analysis Dashboard Users Guide Client Time Analysis Dashboard Users Guide Updated 3/5/11 Page 1 of 5 Client Time Analysis Dashboard The Client Time Analysis Dashboards provide an interactive view of client hours and dollars posted for

More information

Pursuant to the authority vested in the Commissioner of Health by Article 33 of the

Pursuant to the authority vested in the Commissioner of Health by Article 33 of the Electronic Prescriptions and Records for Hypodermic Needles and Hypodermic Syringes Effective date: 10/9/13 Pursuant to the authority vested in the Commissioner of Health by Article 33 of the Public Health

More information

This guide describes the core components of a SMF suitable for a company holding an importer s or wholesaler s licence.

This guide describes the core components of a SMF suitable for a company holding an importer s or wholesaler s licence. Introduction The purpose of the SMF is to provide the Inspector with an introduction to the company and its activities prior to the commencement of the inspection and to demonstrate to the Inspector that

More information

1 OF 6 3. SUBMISSION REQUIREMENTS FOR APPLICATION FOR APPROVAL TO OPERATE A PHARMACEUTICAL BUSINESS

1 OF 6 3. SUBMISSION REQUIREMENTS FOR APPLICATION FOR APPROVAL TO OPERATE A PHARMACEUTICAL BUSINESS 1 OF 6 D R U G S R E G U L A T O R Y U N I T Ministry of Health M i n i s t r y o f H e a l t h H e a d q u a r t e r s F l o o r 3, B l o c k D G o v e r n ment E n c l a ve P / B a g 0 0 3 8 G a b o

More information

Supplements and Amendments VII to the Mainland s Specific Commitments on Liberalization of Trade in Services for Hong Kong 1

Supplements and Amendments VII to the Mainland s Specific Commitments on Liberalization of Trade in Services for Hong Kong 1 Annex Supplements and Amendments VII to the Mainland s Commitments on Liberalization of Trade in Services for Hong Kong 1 Sectors or 1. Business services A. Professional services d. Architectural services

More information

Annex 7 Guidelines on pre-approval inspections

Annex 7 Guidelines on pre-approval inspections World Health Organization WHO Technical Report Series, No. 902, 2002 Annex 7 Guidelines on pre-approval inspections 1. General 94 2. Glossary 94 3. Objectives 95 4. Priorities 96 5. Preparation for the

More information

LICENCE FEES FOR MEDICINAL PRODUCTS FOR HUMAN USE ONLY PROPOSALS FOR APRIL 2002

LICENCE FEES FOR MEDICINAL PRODUCTS FOR HUMAN USE ONLY PROPOSALS FOR APRIL 2002 Fax: 020 7273 0121 To all licence holders and representative associations Dear Sir/Madam Our Ref: MLX/277 15 November 2001 LICENCE FEES FOR MEDICINAL PRODUCTS FOR HUMAN USE ONLY PROPOSALS FOR APRIL 2002

More information

GUIDELINES FOR FOOD IMPORT CONTROL SYSTEMS

GUIDELINES FOR FOOD IMPORT CONTROL SYSTEMS GUIDELINES FOR FOOD IMPORT CONTROL SYSTEMS SECTION 1 SCOPE CAC/GL 47-2003 1. This document provides a framework for the development and operation of an import control system to protect consumers and facilitate

More information

BA-PHALABORWA MUNICIPALITY FLEET MANAGEMENT POLICY 2014/15

BA-PHALABORWA MUNICIPALITY FLEET MANAGEMENT POLICY 2014/15 BA-PHALABORWA MUNICIPALITY FLEET MANAGEMENT POLICY 2014/15 1 POLICY ON MUNICIPAL VEHICLE USAGE TABLE OF CONTENTS CONTENTS 1. Preamble.. 2. Purpose of the policy. 3. Application of the policy.. 4. Regulations

More information

NEW RULES ON FOREIGN EXCHANGE TRANSACTIONS IMPORT, EXPORT AND RE-EXPORT OF GOODS

NEW RULES ON FOREIGN EXCHANGE TRANSACTIONS IMPORT, EXPORT AND RE-EXPORT OF GOODS NEW RULES ON FOREIGN EXCHANGE TRANSACTIONS IMPORT, EXPORT AND RE-EXPORT OF GOODS Notice nr. 19/2012, 19.04., of National Bank of Angola establishes the new regime for foreign exchange transactions relating

More information

Summary of the role and operation of NHS Research Management Offices in England

Summary of the role and operation of NHS Research Management Offices in England Summary of the role and operation of NHS Research Management Offices in England The purpose of this document is to clearly explain, at the operational level, the activities undertaken by NHS R&D Offices

More information

International Trade. Business Advice Open Day 2010 2

International Trade. Business Advice Open Day 2010 2 An Introduction to International Trade Business advice open day 2010 International Trade By the end of this session you will know The basics to International Trade Understand the basic requirements Some

More information

Report to ENVIRONMENTAL PLANNING & REGULATIONS Committee for noting

Report to ENVIRONMENTAL PLANNING & REGULATIONS Committee for noting 15-337 Subject: Prepared by: Regulatory Services Environmental Health Activity Report 1 July - 30 September 2015 Sarwan Kumar (Regulatory Services Manager) Meeting Date: 21 October 2015 Report to ENVIRONMENTAL

More information

Appendix 1 ATTACHMENT A REVISED OPERATIONAL CERTIFICATION PROCEDURES (OCP) FOR THE RULES OF ORIGIN OF THE ASEAN-CHINA FREE TRADE AREA

Appendix 1 ATTACHMENT A REVISED OPERATIONAL CERTIFICATION PROCEDURES (OCP) FOR THE RULES OF ORIGIN OF THE ASEAN-CHINA FREE TRADE AREA Appendix 1 ATTACHMENT A REVISED OPERATIONAL CERTIFICATION PROCEDURES (OCP) FOR THE RULES OF ORIGIN OF THE ASEAN-CHINA FREE TRADE AREA For the purpose of implementing the Rules of Origin for the ASEAN-China

More information

Introduction to the 2015 Horizon 2020 Energy Call for Proposals. 14 July 2014

Introduction to the 2015 Horizon 2020 Energy Call for Proposals. 14 July 2014 Introduction to the 2015 Horizon 2020 Energy Call for Proposals 14 July 2014 Overview Horizon 2020 Overview Energy Challenge Work Programme and Calls for Proposals Horizon 2020 opportunities outside the

More information

Electronic exchanges of individual case safety reports (ICSRs) with ANSM (National Agency of Medicine and Health Product safety)

Electronic exchanges of individual case safety reports (ICSRs) with ANSM (National Agency of Medicine and Health Product safety) Pharmacovigilance information for pharmaceutical companies Electronic exchanges of individual case safety reports (ICSRs) with ANSM (National Agency of Medicine and Health Product safety) This document

More information

II. Business case for Population and Housing Census 2011

II. Business case for Population and Housing Census 2011 Distr. GENERAL Working Paper 9 April 2013 ENGLISH ONLY UNITED NATIONS ECONOMIC COMMISSION FOR EUROPE (ECE) CONFERENCE OF EUROPEAN STATISTICIANS ORGANISATION FOR ECONOMIC COOPERATION AND DEVELOPMENT (OECD)

More information

GCP INSPECTORS WORKING GROUP <DRAFT> REFLECTION PAPER ON EXPECTATIONS FOR ELECTRONIC SOURCE DOCUMENTS USED IN CLINICAL TRIALS

GCP INSPECTORS WORKING GROUP <DRAFT> REFLECTION PAPER ON EXPECTATIONS FOR ELECTRONIC SOURCE DOCUMENTS USED IN CLINICAL TRIALS European Medicines Agency London, 17 October 2007 Doc. Ref. EMEA/505620/2007 GCP INSPECTORS WORKING GROUP REFLECTION PAPER ON EXPECTATIONS FOR ELECTRONIC SOURCE DOCUMENTS USED IN CLINICAL TRIALS

More information

Decree N 152 (24 January 2013) Administrative Measure on Inspection, Quarantine and Supervision of Imports and Exports of Dairy products

Decree N 152 (24 January 2013) Administrative Measure on Inspection, Quarantine and Supervision of Imports and Exports of Dairy products Decree N 152 (24 January 2013) Administrative Measure on Inspection, Quarantine and Supervision of Imports and Exports of Dairy products Chapter 1 General Principle Article 1 In order to enhance inspection,

More information

LOGISTICS, SECURITY AND COMPLIANCE: THE PART TO BE PLAYED BY AUTHORISED ECONOMIC OPERATORS (AEOs) AND DATA MANAGEMENT

LOGISTICS, SECURITY AND COMPLIANCE: THE PART TO BE PLAYED BY AUTHORISED ECONOMIC OPERATORS (AEOs) AND DATA MANAGEMENT LOGISTICS, SECURITY AND COMPLIANCE: THE PART TO BE PLAYED BY AUTHORISED ECONOMIC OPERATORS (AEOs) AND DATA MANAGEMENT Abstract Doug Tweddle Enhanced security, compliance and logistics management in both

More information

OF THE INTERGOVERNMENTAL WORKING GROUP ON THE MULTILATERAL EVALUATION MECHANISM (MEM)

OF THE INTERGOVERNMENTAL WORKING GROUP ON THE MULTILATERAL EVALUATION MECHANISM (MEM) THIRD MEETING OF THE INTERGOVERNMENTAL OEA/Ser.L./XIV.4.3 WORKING GROUP ON THE MULTILATERAL CICAD/MEM/doc.14/98 rev. 1 EVALUATION MECHANISM (MEM) 4 December 1998 October 26-28, 1998 Original: Spanish Tegucigalpa,

More information

How To Inspect A Blood Bank

How To Inspect A Blood Bank Site visit inspection report on compliance with HTA minimum standards Belfast Cord Blood Bank HTA licensing number 11077 Licensed for the procurement, processing, testing, storage, distribution and import/export

More information

How To Understand And Understand The Rules Of International Civil Aviation

How To Understand And Understand The Rules Of International Civil Aviation Introduction and recent changes to ICAO provisions and guidance Dr Anthony Evans Chief Aviation Medicine International Civil Aviation Organization Bucharest, Romania November, 2013 12 November 2013 Page

More information

THE DRUGS AND COSMETICS RULES, 1945

THE DRUGS AND COSMETICS RULES, 1945 THE DRUGS AND COSMETICS RULES, 1945 PART VI SALE OF DRUGS OTHER THAN HOMOEOPATHIC MEDICINES 59. (1) The State Government shall appoint Licensing Authorities for the purpose of this Part for such areas

More information

Douane is changing New legislation 1-1-2011

Douane is changing New legislation 1-1-2011 Douane Belastingdienst Douane is changing New legislation 1-1-2011 Businesses Saba & Sint Eustatius 1 Douane is changing The public bodies, Saba and Sint Eustatius, are on the verge of an important change

More information

Thurrock Council JOB PROFILE. Team Leader Surveying and Engineering

Thurrock Council JOB PROFILE. Team Leader Surveying and Engineering JOB PROFILE DIRECTORATE JOB TITLE POST NUMBER Housing Electrical Engineer T07 GRADE Band 7 RESPONSIBLE TO KEY LIAISON WITH Team Leader Surveying and Engineering Housing Management, Contract Managers, Quality

More information

White Paper The EU Clinical Trials Regulation Main Changes and Challenges

White Paper The EU Clinical Trials Regulation Main Changes and Challenges White Paper The EU Clinical Trials Regulation Main Changes and Challenges Table of Contents 1. Introduction... 3 2. Main Changes and Associated Challenges... 4 2.1 Procedure for Initial Authorisation...

More information

Annex 9 Guide to good storage practices for pharmaceuticals 1

Annex 9 Guide to good storage practices for pharmaceuticals 1 World Health Organization WHO Technical Report Series, No. 908, 2003 Annex 9 Guide to good storage practices for pharmaceuticals 1 1. Introduction 125 2. Glossary 126 3. Personnel 128 4. Premises and facilities

More information

Virginia Board of Pharmacy. Returned check fee increase

Virginia Board of Pharmacy. Returned check fee increase Virginia Board of Pharmacy Returned check fee increase REGULATIONS GOVERNING THE PRACTICE OF PHARMACY 18VAC110-20-20. Fees. A. Unless otherwise provided, fees listed in this section shall not be refundable.

More information

FASFC policy on food safety in the short supply chain

FASFC policy on food safety in the short supply chain Symposium Scientific Committee of the Belgian Food Safety Agency Food Safety of the Short Supply Chain Brussels, 9 november 2012 FASFC policy on food safety in the short supply chain Herman Diricks Director-general

More information

Guideline on good pharmacovigilance practices (GVP)

Guideline on good pharmacovigilance practices (GVP) 9 April 2013 EMA/816573/2011 Rev 1* Guideline on good pharmacovigilance practices (GVP) Module II Pharmacovigilance system master file (Rev 1) Draft of first version finalised by the Agency in collaboration

More information

I m awash in reports, how do I access clear information? Sentry Data Systems Saves You Time and Money

I m awash in reports, how do I access clear information? Sentry Data Systems Saves You Time and Money Medicaid is telling me to include an NDC on my outpatient claims. How can I do that accurately? Who can I trust to really solve my 340B and Own Use compliance issues? Am I really maximizing the financial

More information

Guidance for Industry What You Need To Know About Registration of Food Facilities Small Entity Compliance Guide

Guidance for Industry What You Need To Know About Registration of Food Facilities Small Entity Compliance Guide Guidance for Industry What You Need To Know About Registration of Food Facilities Small Entity Compliance Guide Additional copies are available from: Office of Compliance, HFS-607 Center for Food Safety

More information

DEA Washington Division Diversion Control Program

DEA Washington Division Diversion Control Program SOUTHWEST VIRGINIA PRESCRIPTION DRUG ABUSE SUMMIT DEA Washington Division Diversion Control Program Mary Johnson-Rochee Diversion Program Manager November 14, 2012 Topics: DEA s Diversion Mission How DEA

More information

VAT guide for small businesses. VAT guide

VAT guide for small businesses. VAT guide VAT guide Contents VAT guide for small businesses What is VAT? Contents What is VAT? VAT, or Value Added Tax, is a tax that is charged on most goods and services that VAT registered businesses provide

More information

Thepurposeofahospitalinformationsystem(HIS)istomanagetheinformationthathealth

Thepurposeofahospitalinformationsystem(HIS)istomanagetheinformationthathealth FederatedDatabaseSystemsforReplicatingInformationin UniversityofDortmund,DepartmentofComputerScience,Informatik10 ExtendingtheSchemaArchitectureof E-mail:willi@ls10.informatik.uni-dortmund.de HospitalInformationSystems

More information

NIH Loan Repayment Program. Shawn M. McClintock, PhD, MSCS Associate Professor Duke University School of Medicine UT Southwestern Medical Center

NIH Loan Repayment Program. Shawn M. McClintock, PhD, MSCS Associate Professor Duke University School of Medicine UT Southwestern Medical Center NIH Loan Repayment Program Shawn M. McClintock, PhD, MSCS Associate Professor Duke University School of Medicine UT Southwestern Medical Center Overview Personal Career Journey NIH Loan Repayment Program

More information

Product Liability Insurance Proposal Form

Product Liability Insurance Proposal Form Product Liability Insurance Proposal Form Notes: Statement pursuant to Section 25(5) of the Insurance Act (Cap 142) or any amendments thereof: you are to disclose in the application, fully and faithfully,

More information

This document is meant purely as a documentation tool and the institutions do not assume any liability for its contents

This document is meant purely as a documentation tool and the institutions do not assume any liability for its contents 2002R0178 EN 30.06.2014 005.001 1 This document is meant purely as a documentation tool and the institutions do not assume any liability for its contents B REGULATION (EC) No 178/2002 OF THE EUROPEAN PARLIAMENT

More information

EN 1 EN COMMUNICATION FROM THE COMMISSION. to the European Parliament and the Council on a EU Drugs Action Plan (2005-2008) Introduction

EN 1 EN COMMUNICATION FROM THE COMMISSION. to the European Parliament and the Council on a EU Drugs Action Plan (2005-2008) Introduction MUNICATION FROM THE MISSION to the European Parliament and the Council on a EU Drugs Action Plan (2005-2008) Introduction The drugs phenomenon is one of the major concerns of the citizens of Europe and

More information

NH Laws / Rules Regarding Limited Retail Drug Distributors

NH Laws / Rules Regarding Limited Retail Drug Distributors NH Laws / Rules Regarding Limited Retail Drug Distributors 318:1, VII-a. "Limited retail drug distributor'' means a distributor of legend devices or medical gases delivered directly to the consumer pursuant

More information

Quarantine Requirements for the Importation of Laboratory Animals

Quarantine Requirements for the Importation of Laboratory Animals Appendix 1-8 Quarantine Requirements for the Importation of Laboratory Animals (In case of any discrepancy between the English version and the Chinese text of these Requirements, the Chinese text shall

More information

Good Manufacturing Practices for the Production of Packaging Inks formulated for use on the non food contact surfaces of food packaging and articles

Good Manufacturing Practices for the Production of Packaging Inks formulated for use on the non food contact surfaces of food packaging and articles Good Manufacturing Practices for the Production of Packaging Inks formulated for use on the non food contact surfaces of food packaging and articles intended to come into contact with food October 2005

More information

Merge ICD 10 FAQ. September 2013. Table of Contents

Merge ICD 10 FAQ. September 2013. Table of Contents Merge ICD 10 FAQ September 2013 Table of Contents Overview... 2 Merge RIS... 3 Merge Fusion RIS... 3 Merge Financials... 4 Sentinel... 4 Merge Cardio... 5 Merge Hemo... 5 Merge OrthoEMR... 6 Merge LIS...

More information

Manuel Velazquez April 09 ID:# 14266336

Manuel Velazquez April 09 ID:# 14266336 Mexico: Certificate of Free Sale Page 1 of 5 Manuel Velazquez April 09 ID:# 14266336 Summary It is very important to know in advance the documents required by the Mexican Customs Agency to exports into

More information

Quote Upload and Estimates Tool (QUE)

Quote Upload and Estimates Tool (QUE) Quote Upload and Estimates Tool (QUE) Smart Care Estimates Tool V1.7 UPDATED: March 17, 2011 Copyright Cisco systems, Inc. All rights reserved Page: 1 TABLE OF CONTENTS ABOUT THIS DOCUMENT...4 INTRODUCTION...4

More information

Report of the. Review Committee on Regulation of Pharmaceutical Products in Hong Kong

Report of the. Review Committee on Regulation of Pharmaceutical Products in Hong Kong Report of the Review Committee on Regulation of Pharmaceutical Products in Hong Kong Food and Health Bureau December 2009 CONTENT Executive Summary i Chapter 1 Chapter 2 Chapter 3 Chapter 4 Chapter 5 Chapter

More information

House Study Bill 503 - Introduced

House Study Bill 503 - Introduced House Study Bill 0 - Introduced HOUSE FILE BY (PROPOSED COMMITTEE ON HUMAN RESOURCES BILL BY CHAIRPERSON MILLER) A BILL FOR An Act relating to prescription authority for certain psychologists and making

More information

CARSWELL LEGAL SOLUTIONS SMART CORPORATE AND LITIGATION SOLUTIONS FROM CYBERBAHN AND MARQUE D OR

CARSWELL LEGAL SOLUTIONS SMART CORPORATE AND LITIGATION SOLUTIONS FROM CYBERBAHN AND MARQUE D OR CARSWELL LEGAL SOLUTIONS SMART CORPORATE AND LITIGATION SOLUTIONS FROM CYBERBAHN AND MARQUE D OR Phone: 514 393-9900 1 800 668-0668 FAX: 514 393-4060 Send completed form at the following address: mdo.info@thomsonreuters.com

More information

Legal actions & practice against wrongdoers in the hungarian medicinal market

Legal actions & practice against wrongdoers in the hungarian medicinal market Legal actions & practice against wrongdoers in the hungarian medicinal market 15th May, 2012. Dr. Nánay János András National Institute for Quality and Organizational Development in Healthcare and Medicines

More information

Report to the Commission on Narcotic Drugs on Supporting recovery from substance use disorders

Report to the Commission on Narcotic Drugs on Supporting recovery from substance use disorders American Model United Nations Commission on Narcotic Drugs Report to the Commission on Narcotic Drugs on Supporting recovery from substance use disorders Contents 1 Executive Summary 2 2 Matters calling

More information

UPS Canada Brokerage Rates Effective January 2, 2012

UPS Canada Brokerage Rates Effective January 2, 2012 UPS Canada Brokerage Rates Effective January 2, 2012 2012 Rates How to Use This Guide SECTION 1 How To Pages 3 9 SECTION 2 Shipping Services and Rates Pages 10 43 SECTION 3 Import Rates into Canada Pages

More information

NHS GP Manchester NVUG Panel Member GP /Pharmacy Advisory group to CFH for the NHS Electronic Prescription Service CFH EPS National Clinical Lead

NHS GP Manchester NVUG Panel Member GP /Pharmacy Advisory group to CFH for the NHS Electronic Prescription Service CFH EPS National Clinical Lead NHS GP Manchester NVUG Panel Member GP /Pharmacy Advisory group to CFH for the NHS Electronic Prescription Service CFH EPS National Clinical Lead 2008-10 Trafford PCT Clinical Lead for EPS on the implementation

More information

COMMITTEE FOR PROPRIETARY MEDICINAL PRODUCTS (CPMP) COMMITTEE FOR VETERINARY MEDICINAL PRODUCTS (CVMP)

COMMITTEE FOR PROPRIETARY MEDICINAL PRODUCTS (CPMP) COMMITTEE FOR VETERINARY MEDICINAL PRODUCTS (CVMP) European Medicines Agency Veterinary Medicines and Inspections London, 15 April 2005 EMEA/CVMP/134/02 Rev 1 CPMP/QWP/227/02 Rev 1 COMMITTEE FOR PROPRIETARY MEDICINAL PRODUCTS (CPMP) COMMITTEE FOR VETERINARY

More information

Comparative analysis between the possible regulatory approaches to GMP compliance TITOLO PRESENTAZIONE

Comparative analysis between the possible regulatory approaches to GMP compliance TITOLO PRESENTAZIONE Comparative analysis between the possible regulatory approaches to GMP compliance TITOLO PRESENTAZIONE Dr. Fulvio CARLOTTI, GNOSIS SpA, Corporate QA Director September 26, 2014 Scope of GMP GMP compliance

More information

Welcome to the topic on managing delivery issues with Goods Receipt POs.

Welcome to the topic on managing delivery issues with Goods Receipt POs. Welcome to the topic on managing delivery issues with Goods Receipt POs. In this topic, we will explore how to receive incorrect shipments from a vendor in a goods receipt PO document. Sometimes your supplier

More information

GUIDELINES FOR DRUG DONATIONS. A WHO/ Government of Vanuatu guide for those accepting and making donations of drugs.

GUIDELINES FOR DRUG DONATIONS. A WHO/ Government of Vanuatu guide for those accepting and making donations of drugs. INTRODUCTION GUIDELINES FOR DRUG DONATIONS A WHO/ Government of Vanuatu guide for those accepting and making donations of drugs. Why do we need guidelines on the donation of drugs Donations of medicines

More information

IN-DEPTH GUIDE TO THE ORDINARY ACCOUNTING MANAGEMENT SCHEME

IN-DEPTH GUIDE TO THE ORDINARY ACCOUNTING MANAGEMENT SCHEME WWW.SARDEGNAIMPRESA.EU IN-DEPTH GUIDE TO THE ORDINARY ACCOUNTING MANAGEMENT SCHEME BY BIC SARDEGNA SPA 1 LIST OF CONTENTS INTRODUCTION... 3 REQUIREMENTS... 3 THE ACCOUNTING AND TAX FORMALITIES: THE COMPULSORY

More information

Animal health requirements for the exported pig meat, etc. to Japan from Spain are as follows.

Animal health requirements for the exported pig meat, etc. to Japan from Spain are as follows. Animal health requirements for meat and viscera derived from pigs and sausages, ham and bacon made from the said meat and viscera as raw materials to be exported to Japan from Spain Animal health requirements

More information

GUIDANCE DOCUMENT ON THE EVALUATION OF NEW ACTIVE SUBSTANCE DATA POST APPROVAL

GUIDANCE DOCUMENT ON THE EVALUATION OF NEW ACTIVE SUBSTANCE DATA POST APPROVAL 1 EUROPEAN COMMISSION HEALTH & CONSUMER PROTECTION DIRECTORATE-GENERAL Directorate E Safety of the food chain Unit E.3 - Chemicals, contaminants, pesticides SANCO/10328/2004 rev 8 24.01.2012 GUIDANCE DOCUMENT

More information

Competentes en Medicamentos

Competentes en Medicamentos VIII Encuentro de Autoridades Competentes en Medicamentos de los Países Iberoamericanos (EAMI) 12-14 de Mayo 2010 Madrid MARTIN TERBERGER Jefe de la Unidad de Productos Farmacéuticos Nuevas iniciativas

More information

REPORT ON ACTIVITIES IMPLEMENTED IN THE PROJECT TO ESTABLISH PSC

REPORT ON ACTIVITIES IMPLEMENTED IN THE PROJECT TO ESTABLISH PSC REPUBLIC OF SLOVENIA MINISTRY OF JUSTICE AND PUBLIC ADMINISTRATION Tržaška cesta 21, 1000 Ljubljana T: 01 478 83 30 F: 01 478 83 31 E: gp.mju@gov.si www.mju.gov.si REPORT ON ACTIVITIES IMPLEMENTED IN THE

More information

2016 POST-DOCTORAL PROGRAM Applicant Guide

2016 POST-DOCTORAL PROGRAM Applicant Guide 2016 POST-DOCTORAL PROGRAM Applicant Guide POST-DOCTORAL FELLOWSHIP PROGRAM 2016 Applicant guide The Initiative of Excellence of the University of Bordeaux (IdEx Bordeaux) is opening positions for postdoctoral

More information

The Human Medicines Regulations 2012

The Human Medicines Regulations 2012 STATUTORY INSTRUMENTS 2012 No. 1916 MEDICINES The Human Medicines Regulations 2012 Made - - - - 19th July 2012 Laid before Parliament 24th July 2012 Coming into force - - 14th August 2012 38.00 STATUTORY

More information

Electronic medical records

Electronic medical records Electronic medical records Country: France Partner Institute: Institut de Recherche et Documentation en Economie de la Santé (IRDES), Paris Survey no: (8)2006 Author(s): Chantal Cases, Philippe Le Fur

More information

Japan - A Model For Joint Projects

Japan - A Model For Joint Projects Appendix A April 9 th, 2015 JETRO PARIS Application Guidelines for The FY2015 Lead Generation Project on Promotion of Foreign Direct Investment into Japan ( Industry Specialists in Fr acne) The Japan External

More information

~ icon. cancer care. TGA Submission: Options for reform of the regulatory framework for pharmacy compounding

~ icon. cancer care. TGA Submission: Options for reform of the regulatory framework for pharmacy compounding ~ icon cancer care TGA Submission: Options for reform of the regulatory framework for pharmacy compounding Introduction Icon Cancer Care is pleased to have the opportunity to make this submission regarding

More information

Draft guidance for registered pharmacies preparing unlicensed medicines

Draft guidance for registered pharmacies preparing unlicensed medicines Draft guidance for registered pharmacies preparing unlicensed medicines January 2014 1 The General Pharmaceutical Council is the regulator for pharmacists, pharmacy technicians and registered pharmacies

More information

APPLICATION FOR A PERMIT TO Import, Export, or Re-export Live Animals or Animal Parts or Products

APPLICATION FOR A PERMIT TO Import, Export, or Re-export Live Animals or Animal Parts or Products APPLICATION FOR A PERMIT TO Import, Export, or Re-export Live Animals or Animal Parts or Products CITES Form A1 (2014.02.04) CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA

More information

REGULATORY ENVIRONMENT

REGULATORY ENVIRONMENT 1. Introduction REGULATORY ENVIRONMENT Research and development work, pre-clinical tests, clinical studies, facilities, and the manufacture and sale of the Company s products are and will continue to be

More information

EU Clinical Trials Register. www.clinicaltrialsregister.eu. An agency of the European Union

EU Clinical Trials Register. www.clinicaltrialsregister.eu. An agency of the European Union EU Clinical Trials Register www.clinicaltrialsregister.eu An agency of the European Union The EU Clinical Trials Register provides public access to information from the European Union (EU) clinical trial

More information