Embed Size (px)
Citation preview
Patent Related Flexibilities in the Pharmaceutical FieldWorkshop for the GCC on the Protection of Invention in the Pharmaceutical Sector, Patents, Undisclosed Information and Health Policies
Riyadh, Saudi Arabia15-16 October 2012
Marco Aleman
Deputy Director, Patent Law Division, and head, Legislative and Policy Advice Section
Giulia Ragonesi
Consultant, WIPO
WTO/TRIPS
Trips Agreement provides minimum standards of protection of IPRs
WTO members shall provide patents for any invention:- Products (e.g. technical device)- Processes (methods for producing the chemical
ingredients for a medicine)
Definition of Flexibility
“a range of rights, safeguards and options that WTO Members can exploit in their implementation of the TRIPs Agreement”
Vague international rules, that need to be circumscribed in their content by the national legislation
Definition (2)
Idea of “alternative ways” for:
Legislative implementation
To accommodate national interests
It goes without saying that all these ways must be compatible with the provisions and principles of the Treaty
Patents and Public Health
How to strike a balance: using flexibilities
Stimulus of Innovation/R&D
Early and affordable access to new medicines
Patents Generic Drug
Public Health related flexibilities
Exhaustion
Transitional period
Research exception
Regulatory Review (Bolar)
exception
Compulsory licenses
Exhaustion (Art. 6 TRIPs)
Right of the patent holder « exhausted » once the product incorporating the patented invention is put into the market
Exhaustion
National Regional International
Example of national exhaustion
country A
Local price $ 1.0
country B
Local price $ 0.75
country C
Local price $ 1.50
country D
Local price $ 2.00
country E
Local price $ 0,50
Example of international exhaustion
Importing country A
Local price $ 1.0
Exporting country B
Local price $ 0.75
Exporting country C
Local price $ 1.50
Exporting country D
Local price $ 2.00
Exporting country E
Local price $ 0,50
Example of regional exhaustion
country A
Local price $
1.75
country B
Local price $ 0.75
country C
Local price $ 2.05
country E
Local price $ 0.50
country D
local price $ 3.0
National exhaustionUNITED ARAB EMIRATES : Section 17 of the Patent Law No. 44 of 12/10/1992 – 1413
17. The rights conferred by a patent or utility certificate shall cover only acts performed for industrial or commercial purposes. They shall not extend to acts in relation to the protected product once it has been sold in the United Arab Emirates. However, if the patent or utility certificate relates also to a specific use of the product, the owner shall have the right to reserve that use for himself.
OMAN: Article 11 C (4) of the Law on Industrial Property Rights of 2008
4 - The rights under the patent shall not extend:
A) to acts in respect of articles which have been put on the market in Oman by the owner of the patent or with his consent, consequently exhausting the patent owner's rights;
International exhaustionJORDAN: Article 37 of the Law on Patents No. 32 of 1999, as last amended by Law No. 71 of 2001“The provisions of this law shall not prevent any person from importing any materials or goods from a third party if that party enjoys the legal protection of the same patent protected in the Kingdom and if that importation is lawful, complies with the principles of commercial competition and fairly takes into account the economic value of the protected patent.”
EGYPT :Article 10 (1) of the Law on the Protection of Intellectual Property Rights No. 82 of 2002A patent shall confer on its owner the right to prevent a third party from exploiting the invention by any means.The right of a patent owner to prevent a third party from importing, using, selling or distributing a product shall lapse when he commercializes the product in any country or authorizes a third party to do so.
Transitional Period for pharmaceuticals
Art. 66 (1) TRIPS
LDCs: time up to 2016 to provide protection for pharmaceutical inventions (if not yet provided)
Art. 65 (4) TRIPS
Developing Countries. Time up to 2005 to provide protection for patents in area of technology not so protectable in the Member territory on the general date of application of the TRIPS Agreement
Research and Regulatory Review (Bolar) exception
Not explicitly provided in the TRIPs but possible to adopt them according to the open clause contained in Art. 30 of the TRIPs Agreement
Research exception: “the exception under which use of patented product for scientific experimentation, during the term of the patent and without consent, is not an infringement”*
Regulatory review (Bolar) exception: acts to carry out equivalency tests for the regulatory approval of products such as generic medicines before the expiration of the relevant patent
*Canada- Patent protection of Pharmaceutical Product
Examples
GCC : Section 14 (1) of the Patent Regulation of the GCC of 1992 (as at 23/04/2002)
“The rights under the patent shall not extend to:
1) Acts done particularly for experimental purposes”
EGYPT : Article 10 no. 1 of the Intellectual Property Law 82 of 2002
“The following shall not be considered as infringements of that right when carried out by third parties:
1) Activities carried out for scientific research purposes.
Examples Bolar
EGYPT : Article 10 (5) of the Intellectual Property Law 82 of 2002“Where a third party proceeds, during the protection period of a product, with its manufacturing, assembly, use or sale, with a view to obtain a marketing license, provided that the marketing starts after the expiry of such a protection period.
JORDAN : Article 21 C of the Patent Act No. 32 of 1999, as last amended by Act No. 71/2001“Notwithstanding any conflicting provision in this law or any other law, all types of scientific research and development and filing applications for obtaining marketing permits carried out before the elapse of the patent protection period shall not be regarded as infringement neither civil nor criminal
Compulsory license (CL) conditions in the TRIPS
CL: Authorization granted by the government to a third party to use the invention without the consent of the patent holder. Conditions
Authorization on individual merits
Prior efforts for voluntary license (possibility to waive this requirement in case of national emergency or other circumstances of extreme urgency)
Limited scope and duration
CL conditions (2)
Non-exclusive and non-assignable
Used predominantly for the supply of domestic market of the Member authorizing such use
Adequate remuneration to the patent holder
CL and local production
Problem in case of countries which insufficient or no manufacturing capacities in the pharmaceutical sector: how to use the system of CL?
Doha Declaration on TRIPS Agreement and Public Health
WTO Members recognized:
the gravity of public health problems…, especially those resulting from HIV/AIDS, tuberculosis, malaria and other epidemics
the importance of IP for the development of new medicines and the concern about its effect on prices
WTO Members agreed:
TRIPS shall be interpreted and implemented in a way that supports public-health by promoting ^both access to existing medicines and the creation of new medicines
TRIPS doesn’t and shouldn't prevent members from taking measures to protect public health
Doha Declaration on TRIPS and Public Health (2)
Countries shall use flexibilities contained in the TRIPSEach Member has the right to grant CL and the freedom to determine the ground upon which such licenses are grantedEach Member has the right to determine what constitutes a national emergency or other circumstances of extreme urgencyEach Member is free to establish its own exhaustion regime without challengeExemption for LDCs on pharmaceutical patents until 2016
Paragraph 6 of Doha Declaration
Problem:- Members lacking manufacturing capacities could issue
compulsory licenses for importation- But: Art. 31 (f) requires production “predominantly for the
supply of the domestic market of the member”
Under Paragraph 6 of the Declaration, the General Council mandated the TRIPS Council to find a solution to the issue
The Decision of the General Council of WTO of August 30,2003 (1)
3 distinct waivers granted:- Exporting countries’ obligation under Art. 31 (f). Any
Member can export drugs made under CL to meet the needs of importing countries
- Remuneration is only required on the export side- Exporting constraints are waived
The Decision of the General Council of WTO of August 30,2003 (2)
Paragraph 2 of the decision sets out conditions to comply with:
- Notification of the TRIPS Council- Confirmation of insufficient or no manufacturing
capacities in the pharmaceutical sector (except LDCs)- Determination of expected quantities- Products produced under license shall be clearly
identified- Adopting reasonable measures to prevent re-exportation
of these products
The Decision of the General Council of WTO of August 30,2003 (3)
Eligible importing members:- LDC members automatically eligible- Any other Member eligible, subject to mandatory
notifications- But: 44 Members have voluntarily opted out partially or
fully
Decision of 30 August 2003 is interim, terminates when amendment replaces it for each member
Amendment of the TRIPS Agreement-new Art. 31 bis (December 6,2005)
General Council adopted the Protocol amending the TRIPS Agreement on December 6,2005
The protocol was opened for acceptance by Members until December 1, 2007 and has been extended until 31 December 2009, to 31 December 2011, and then to 31 December 2013*
The amendment will enter into force if 2/3 of eh WTO Members notify their acceptance Currently 43 Countries + EU have accepted
*General Council decisions respectively of 18 December 2007, 17 December 2009 and 30 November 2011
First notification
4 October 2007
Canada has authorized a company to make a generic version of a patented medicine (AIDS therapy drug) for export to Rwanda, which is unable to manufacture the medicine itself
Are patents really a barrier to access to medicines in developing countries?
95% of the products on the WHO Essential Drug List are not patentedAntiretrovirals are not patented in half of the African StatesIn the other half, only 3 out of 16 antiretrovirals are patented total amount of patents 18%. There is no patent on triple therapies12 out of 13 malaria drugs are not patented in Africa total amount of patents 5%9 out of 11 tuberculosis drugs are not patented in Africa total amount of patents 1%
Access to medicines in developing countries
TRIPS forms part of the solution next to the other important factors: infrastructure, national health systems, procurement regimes, reduction import tariffs, etc.
Extra effort needed to address the problem of neglected diseases as patent as incentive does not work due to lack of market
IP must be protected to trigger R&D and further mechanisms must be developed to trigger R&D into neglected diseases.
6. StatisticsNumber of countries which used Transition Periods
0
1
2
3
4
5
6
7
Africa Asia andOceania
Latin Americaand Caribbean
Africa
Asia and Oceania
Latin America andCaribbean
Transition Periods
0
20
40
60
80
100
Africa Asia and Oceania Latin America andCaribbean
Express statement to use the general transition period
Transition Period related to Patent Product Protection
%
Countries analyzed: Exhaustion
0
5
10
15
20
25
30
35
National Regional International
Africa
Latin Americaand Caribbean
Asia andOceania
Europe
OECD
Statistics: Exhaustion
0
10
20
30
40
50
60
70
80
90
National Regional International
Africa
Latin Americaand Caribbean
Asia andOceania
Europe
OECD
%
Countries analyzed: Research and Bolar exception
0
5
10
15
20
25
30
35
40
Africa LatinAmerica
andCaribbean
Asia andOceania
Europe OECD
Research exception
Bolar exception
+
EU
Statistics: Research and Bolar exception
0102030405060708090
100
Africa LatinAmerica
andCaribbean
Asia andOceania
Europe OECD
Research exception
Bolar exception
%
+
EU
Countries analyzed: Compulsory Licenses
05
1015202530354045
Africa LatinAmerica andCaribbean
Asia andOceania
Europe OECDCountries
+
EU
Statistics: Compulsory Licenses (For non-working)
0102030405060708090
100
Africa Latin Americaand Caribbean
Asia andOceania
Europe OECDCountries
%
Statistics: Compulsory Licenses (For dependent patent)
0102030405060708090
100
Africa LatinAmerica andCaribbean
Asia andOceania
Europe OECDCountries
%
Statistics: Compulsory Licenses (To correct patent abuse)
0102030405060708090
100
Africa LatinAmerica andCaribbean
Asia andOceania
Europe OECDCountries
%
Statistics: Compulsory Licenses (For public interest)
0102030405060708090
100
Africa LatinAmerica andCaribbean
Asia andOceania
Europe OECDCountries
%
Statistics: Compulsory Licenses (Government use)
0102030405060708090
100
Africa LatinAmerica andCaribbean
Asia andOceania
Europe OECDCountries
%
Statistics: Compulsory Licenses (Implementation of the Decision of the
General Council)
0102030405060708090
100
Africa LatinAmerica andCaribbean
Asia andOceania
Europe OECDCountries
%
Thank you!
