JOINT SUBMISSION BY SOUTH AFRICAN PHARMACEUTICAL TRADE ASSOCIATIONS TO THE DEPARTMENT OF TRADE AND INDUSTRY

Similar documents
CURRENT ISSUES IN INTELLECTUAL PROPERTY: A PATIENT PERSPECTIVE

IP, LOCAL MANUFACTURING, INDUSTRIAL AND ACCESS POLICIES

Linking Drug Pricing with Pharmaceutical Patents in Canada. Roy Atkinson. Presented by

Annex 1 - APEC OECD Framework on Competition Assessment

UK Action Plan on Business & Human Rights review. TUC submission

SIAPS assistance is grouped into four technical areas

IPRs in the pharmaceutical industry

Effective application of Risk Management techniques to Drug Safety: a pragmatic approach

STRATEGIC PLAN OF THE STATE INSTITUTE FOR DRUG CONTROL FOR Public Section

Country Paper: Coherent Approach to Trade and Regulation of Services: Lessons from India


Global Forum on Competition

To the Department of Trade and Industry (the dti) 11 October Background. For Attention: Ms Meshendri Padayachy,

CSDP Supplier Guidelines

Legislation, Transition and Implementation Medicines Control Council & SA Health Products Regulatory Authority. SAAPI Conference April 2016

Medical Device Regulatory Framework

MEDICINES CONTROL COUNCIL

Relationships with Government

Application for registration certificate to operate a retail pharmacy 5, ,000.00

1. Council conclusions on strengthening the balance in the pharmaceutical systems in the EU and its Member States

Regulatory system strengthening

CHAPTER THE PHARMA LEGAL HANDBOOK SOUTH AFRICA

BRITISH GENERIC MANUFACTURERS ASSOCIATION

New pharmacovigilance systems and services

Please find following our submission. EFA would be pleased to expand on the issues below in oral testimony or otherwise.

THE MARKET IMPACTS OF PRODUCT PATENTS IN DEVELOPING COUNTRIES: EVIDENCE FROM INDIA

IP Audit.an imperative

European Commission s strategy for single market Using Bolar and the SPC Wavier to Stimulate Growth in the EU

COMMUNICATION ON PROGRESS REPORT 2017

Initial Draft Discussion Document for A Canadian Orphan Drug Regulatory Framework

Pills and pocketbooks: Equity pricing of essential medicines in developing countries

Solving the drug patent problem

Voluntary Qualified Importer Program (VQIP) Final Guidance for Industry Overview

ADVANCING THE SINGLE MARKET FOR MEDICINES GIRP Position Paper

Patents & Health. Dr. Brian W Tempest.

4.3 Learning from FLEGT Voluntary Partnership Agreements

Lessons from AMFm how this informs RDT introduction in Private Sector. Vivian N.A. Aubyn NMCP Ghana

December , The US-China Business Council 1

Brexit Guidance for Stakeholders Human and veterinary medicines

ONLINE RESTRAINTS EFFECTS, ANALYSIS AND ENFORCEMENT

PO Box 518, Noordwyk, October 2015

Medicines Control Council & update on SA Health Products Regulatory Authority

Access to High Cost Medicines: Examples from the Americas

On partnership between the United Nations and regional organizations, in particular with the African Union (AU)

Canada s Patented Medicine Prices Review Board. Michelle Boudreau, Executive Director Market Access Summit November 15-16, 2011

WORLD TRADE ORGANIZATION

The SADC Communications Environment

The Anti-monopoly Commission of the State Council. Anti-monopoly Guideline on Abuse of Intellectual Property Rights.

Counterfeit Drugs and Supply Chain Security

Principles for Responsible Agricultural Investment (PRAI) September, 2012 Ministry of Foreign Affairs, Japan 1

SA Code of Marketing Practice Kirti Narsai, PIASA

Policy principles for a competitive healthcare environment

Strengthening development linkages from the mineral resource sector in the Economic Community of Central African States

Technical Briefing Seminar - Pricing Policies

FSC Trademark Use Guide for Promotional Licence Holders: Impact assessment of the revised requirements

Internal Audit and Oversight Division (IAOD) TERMS OF REFERENCE (ToRs) EVALUATION STRATEGIC GOAL VI:

Making generic and biosimilar manufacturing thrive : a global policy. WHO remarks : improving quality and access

Foreign Affairs, Defence and Trade Select Committee Parliament Wellington. 24 March 2016

National Farmers Federation

HNP Brief #3. Pharmaceuticals: Local Manufacturing. March Introduction. Overview of pharmaceutical companies in lowand middle-income countries

UNITAID. Increasing access to quality medicines and diagnostics for HIV/AIDS,TB and Malaria

Strategic and Retail Market Review. 28 February 2008

Executive Compensation

POSITION DESCRIPTION

Regulatory system strengthening for medical products

Pharmaceuticals in a Global Environment

Addressing Perceived Barriers to the Acceptance of Third Party Certification

Building Product Innovation Capability in Health

Genetic Resources in Biodiversity Conservation and Sustainable Development in a Changing World Order

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

Original language: English CoP16 Doc. 19 (Rev. 1) CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA

The Future of Pharmaceuticals for Human Use in Europe Cefic Input to the Consultation Process: Deadline for Submission 12/10/2007 Date: 10/10/07

Advancing affordability to connect the last 50%

Arms Trade Treaty and Biological Weapons Convention. Hon. Francisco Ashley Acedillo Representative, Magdalo Party-list House of Representatives

1. Introduction. 2. Background

Pearson Education Limited Edinburgh Gate Harlow Essex CM20 2JE England and Associated Companies throughout the world

Medical Device Regulatory Framework 9 SEPTEMBER 2015 FUNDISA CONFERENCE JANE ROGERS

EXXARO SUPPLIER CODE OF CONDUCT

Id. 3. Id. Docket # USTR Edward Gresser Chair of the Trade Policy Staff Committee Office of the United States Trade Representative

LAW of UKRAINE. No III. On Standardization

COMMITTEE ON WORLD FOOD SECURITY

Introduction to the Generic Drug Supply Chain and Key Considerations for Policymakers

TWN. Third World Network. Expert group meeting on the agenda-setting for the High-Level Political Forum (HLPF) 30 April 2014, New York

Guidelines on import procedures for pharmaceutical products

Improved Food Inspection Model The Case for Change

Regional Perspective on Gas Sector Policy and Institutional Framework

R&D as a public good and the delinking of product prices from the R&D costs, including cost of the incentives to inducement investments

Action points and notes. UNFPA, UN House, Copenhagen Denmark

Codex Alimentarius Commission STRATEGIC FRAMEWORK

DIGITAL EDITION BONUS CONTENT

Proposal for process of consultation on principles for responsible agricultural investments (RAI) within the CFS

Legislative and Regulatory Modernization for Therapeutic Products

2. Market access issues relating to Beef, Pork and Poultry

Submission to the Department of Foreign Affairs and Trade on the Regional Comprehensive Economic Partnership

Annual Performance Plan 2018/19. Tembinkosi Bonakele, Commissioner 17 April 2018 Presentation to the Portfolio Committee on Economic Development

Proclamations Proklamasies

Evaluation: annual report

Work stream 6: Regional growth for southern Africa s prosperity

Common Vision Common Future Be sustainable. Be economically viable. FISHERIES RENEWAL FRAMEWORK Action Plan

Council of the European Union Brussels, 30 November 2017 (OR. en)

Transcription:

JOINT SUBMISSION BY SOUTH AFRICAN PHARMACEUTICAL TRADE ASSOCIATIONS TO THE DEPARTMENT OF TRADE AND INDUSTRY October 2005 1

Introduction South Africa has, as a country, taken a different approach to address the challenges facing it, the most prominent that of transition to democracy, of macro-economic development and of addressing its main social challenges. To this end South Africa has learnt the lessons of constructive engagement and taking a non-confrontational stance that has made it perhaps one of the leaders in finding solutions and preventing a downward spiraling of conflict. It is perhaps this unique history and the continuation of the same approach and attitude to engagement with government and other stakeholders that underpins this submission and has led to South Africa adopting creative and pragmatic solutions to those situations that risk conflict. This submission is made jointly by the following collective SA pharmaceutical manufacturers, importers and industry organizations, representing in excess of 95% of the South African market in value terms: Innovative Medicines SA (IMSA) National Pharmaceutical Manufacturers Association (NAPM) Pharmaceutical Manufacturers Association (PMA) The parties have recently demonstrated this positive attitude to constructive engagement with the Department of Health, by participating in key activities and supporting the achievement of key Departmental objectives, such as the medicines pricing regulations and the draft Health Charter. In the interests of optimal patient access to medicines, this submission seeks to strike a balance between unique challenges of national public health, a sustainable supply of medicines and the protection of the rights associated with intellectual property. Principles The industry associations that make this joint submission endorse the following: Intellectual property rights in general and upholding the South African intellectual property system in particular. Striking a balance in cases of national public health emergencies, between access to healthcare and rights associated with intellectual property. Ensuring that patient safety and quality are never compromised. 2

By using this approach SA could provide a more positive climate for fostering and strengthening foreign direct investment 1 and increased exports. The substance and principles that underpin the Motta decision and Menon Statement. Alternative approaches to address access in national public health emergencies have worked in South Africa The parties to this submission regard voluntary licensing as a preferred route to that of compulsory licensing in order to address access to medicines in national public health emergencies. Voluntary licences, as opposed to compulsory licences, have proved more pragmatic and have achieved the desired objectives of enhancing access and significantly reducing the cost of patented medicines required in such national public health emergencies. The system has been used to ensure that there is more than one supplier, thus assuring continuity of supplies particularly where continuity of treatment is essential. The voluntary licensing approach ameliorates the risk of increased tension and the likelihood of conflict in the investment sector and its health-subsector in particular. South Africa has already achieved significant price decreases on an ex manufacturer level for the private market (21% 2 ). Apart from the medicines pricing system, South Africa has various other domestic mechanisms, ranging from the constitutional mandate to progressively realize access to healthcare, to measures flowing from the 1997-amendments to the Medicines Act and the Broadbased Black Economic Empowerment Act to address issues of access. The government s rollout of ARV s together with the implementation of various models of voluntary licensing in the field of HIV, are two factors that have increased access to medicines. It is estimated that some 110 000 115 000 SA patients can now access ARV s through products using both the original- and voluntary licenced products. This effect is further enhanced by the introduction of a transparent price system and the full implementation of a Single Exit Price on a manufacturer level. A combination of patented and voluntary licensed products can currently service all the patients in this country. IP protection does not present a barrier to access. Other 1 South Africa is currently not among the top 10 African investment destinations UNCTAD 2005 World Investment Report, on FDI outflows South Africa is nr 1. 2 The data used in the calculation was extracted from the following sources: Units: The audits of the global company IMS, Total Pharmaceutical Market January 2004 Prices: Pharmaceutical Computer Data supplied the medicine prices (SEP or pharmacy purchase price) The SEP is the ex manufacturer selling price that includes wholesale and distribution fees, i.e. does not account for retail sector. 3

barriers, such as stigmatization of people living with HIV, still affect the uptake of ARV treatment thereby hampering effective access. In national public health emergencies, voluntary licences and IP sharing agreements increase access to medicines without the negative impact that compulsory licensing may have on investment and growth. The parties agree that there can be grave repercussions to using compulsory licensing as a mechanism to address such emergencies, leading to a negative spiral whereby compulsory licensing leads to tension between stakeholders, 3 and possible subsequent threats and litigation. It can also lead to passive investors that causes negative investment and, may eventually, lead to disinvestment and loss of skills and technology to the country. This, in turn, can lead to patients having less, instead of increased, access to healthcare and to negative growth, with a loss in both up and downstream benefits brought by the pharmaceutical industry. In Brazil, for example, the threat of using compulsory licensing may lead to the potential for access to 2 nd line drug-resistant HIV treatment being significantly affected. Voluntary licencing provides a win-win for all the stakeholders in therapeutic areas that constitute national public health emergencies, i.e. patients, the state, South African business and the investor community, clinicians, the pharmaceutical industry, and above all can achieve all of this by upholding international IPR treaties and South Africa s multilateral trade obligations. Voluntary licenses also allow the parties to maintain the standards of pharmacovigilance reporting that is necessary in the interest of all patients. However, it is important to state that such voluntary licences should be truly voluntary on the basis of each party being a willing participant, with a variety of options to be available to suit the specific nature of the parties and particularities of the national public emergency. South African case studies Agreements representing various forms of sharing of intellectual property, to the benefit of public health emergencies, exist. These range from full technology transfer and empowerment, to licensing to manufacture, and use of patents. Examples of successful IP sharing includes - Lilly & Aspen (fully licenced technology transfer agreement) 3 Within the broader manufacturing, and investment sector and with government departments, most notably DoH and DTI. 4

BMS not enforcing their patent and Cipla Medpro manufacturing generic of stavudine Aspen patent use agreement with BMS MSD & Aspen Gilead Sciences & Aspen (full technology transfer agreement) Agreements may cover a large number of companies throughout Africa if this has been negotiated as part of the voluntary licensing agreement. There is an ongoing interest in these types of arrangements as an option to deal with national public health emergencies. Conclusion The parties that make this submission believe there are creative ways of addressing access to healthcare that could go beyond the current international legal wrangles and supersede conflict in order to address the healthcare needs, and transformational needs of South Africa. We would recommend that the use of voluntary licensing as a first step where ever possible in cases of national public health emergencies. We also regard the inclusion of the Motta text and Menon statement in the TRIPS Agreement as providing the required balance between access to health care and protection of the rights associated with intellectual property in cases of national public health emergencies, were no other mechanisms are available domestically. 5