List of tables
|
xii |
Acknowledgements
|
xiii |
Table of cases
|
xiv |
List of Treaties, Declarations and Resolutions
|
xxii |
List of Statutes
|
xxvi |
List of abbreviations
|
xxxi |
1 Introduction
|
1 |
1.1 Relationship between sustainable development and access to knowledge
|
1 |
1.2 Role of intellectual property rights in restricting access to knowledge
|
12 |
1.3 Purpose and plan of the work
|
15 |
1.4 Methodological approach
|
24 |
Part I Determining the normative meaning of the general exception clauses of the TRIPS Agreement
|
27 |
2 The customary rules of treaty interpretation and the elements in light of which the general exception clauses of TRIPS should be interpreted
|
29 |
Introduction
|
29 |
2.1 Ordinary meaning attributable to the terms of the treaty
|
32 |
2.2 Principle of good faith
|
33 |
2.2.1 Principle of effectiveness in the interpretation of treaties
|
34 |
2.2.2 Doctrine of abuse of rights
|
36 |
2.3 Object and purposes of the WTO system and the TRIPS Agreement
|
39 |
2.3.1 General objectives of the WTO system
|
41 |
2.3.2 Specific objectives of the TRIPS Agreement
|
42 |
2.3.3 Article 8 of the TRIPS Agreement and the guiding principles of the general exception clauses
|
44 |
2.3.3.1 Objectives pursued by the exceptions to IPRs
|
45 |
2.3.3.2 The necessity standard
|
46 |
2.3.3.2.1 The transformation of the necessity standard into a proportionality test
|
54 |
2.3.3.2.2 The necessity standard in the context of art. 8 of the TRIPS Agreement
|
61 |
2.3.3.3 The consistency standard of art. 8 of the TRIPS Agreement
|
63 |
2.3.3.3.1 Additional obligations that shall be observed by copyright exceptions
|
64 |
2.3.3.3.2 Additional obligations that shall be observed by the exceptions to the rights conferred by trademarks
|
66 |
2.3.3.3.3 Additional obligations that shall be observed by the exceptions to the rights conferred by protected industrial designs
|
66 |
2.3.3.3.4 Additional obligations that shall be observed by the exceptions to the exclusive rights conferred by a patent
|
67 |
2.3.3.3.4.1Guarantee of protection to all categories of inventions that shall be protected by all WTO Members
|
67 |
2.3.3.3.4.2Minimum term of protection of patents
|
68 |
2.3.3.3.4.3Respect for the area occupied by the TRIPS compulsory licensing system
|
68 |
2.3.3.3.4.4Non-discrimination based on national origins, the field of technology and the manner of exploitation of the invention
|
70 |
2.4 Context of the general exception clauses of the TRIPS Agreement
|
74 |
2.4.1 Interpretative agreements and subsequent State practices
|
75 |
2.4.2 Rules of international law applicable in the relations between the parties
|
78 |
2.4.2.1 Principle of proportionality
|
82 |
2.5 Supplementary means of interpretation
|
87 |
3 Determining the normative meaning of arts. 17, 26(2) and 30 of the TRIPS Agreement
|
90 |
3.1 Introduction
|
90 |
3.2 Art. 30 of TRIPS according to Canada – Pharmaceutical Patents
|
90 |
3.2.1 The first step of the test of art. 30
|
91 |
3.2.2 The second step of the test of art. 30
|
93 |
3.2.3 The third step of the test of art. 30
|
95 |
3.2.4 Obstacles created by Canada – Pharmaceutical Patents
|
96 |
3.3 Reframing the meaning of art. 30 in the light of the treaty interpretation rules of the VCLT
|
97 |
3.3.1 The first step of the test
|
97 |
3.3.2 The second step of the test
|
100 |
3.3.3 The third step of the test
|
103 |
3.3.4 Summary of the normative meaning of art. 30 resulting from the application of the general rule of interpretation of the VCLT
|
107 |
3.4 Assessment test of the legitimacy of exceptions to the rights conferred by trademarks (art. 17)
|
108 |
3.5 Assessment test of the legitimacy of exceptions to the rights conferred by protected industrial designs (art. 26.2)
|
114 |
4 Determining the normative meaning of art. 13 of the TRIPS Agreement and art. 9(2) of the Berne Convention
|
117 |
4.1 Introduction
|
117 |
4.2 Art. 13 of TRIPS according to US – Section 110(5) Copyright Act
|
121 |
4.2.1 First step: exceptions shall be confined to certain special cases
|
121 |
4.2.2 Second step: exceptions shall not conflict with a normal exploitation of the affected works
|
122 |
4.2.3 Third step: exceptions shall not unreasonably prejudice the legitimate interests of the copyright holders concerned
|
124 |
4.2.4 Why US – Section 110(5) Copyright Act is legally irrelevant to future disputes
|
124 |
4.3 Interpreting art. 13 TRIPS and art. 9(2) BC in accordance with the customary rules of treaty interpretation
|
127 |
4.3.1 The first step
|
127 |
4.3.2 The second step
|
130 |
4.3.3 The third step
|
136 |
4.3.4 Aids offered by the records of the Stockholm Revision Conference
|
140 |
Concluding remarks on Part I
|
148 |
Part II Putting to the test the capacity of the general exception clauses of the TRIPS Agreement to promote the pillars of sustainable development
|
157 |
5 Patents and the R&D and genetic diagnostic test exceptions
|
159 |
5.1 Introduction
|
159 |
5.2 Potential obstacles set by biotech patents to the progress of science and technology
|
163 |
5.2.1 Challenges created by gene patents
|
163 |
5.2.2 Patents on genes associated with disease and genetic tests
|
168 |
5.2.3 Genes and unique resources
|
171 |
5.2.4 Research tools
|
172 |
5.2.4.1 Definition
|
172 |
5.2.4.2 Problems caused by granting patents on research tools
|
173 |
5.2.5 Tragedy of the anti-commons
|
176 |
5.2.6 Royalty stacking
|
177 |
5.3 Research use exception and freedom in science and technology
|
178 |
5.4 Research use exceptions adopted by some members of the international community
|
182 |
5.5 The R&D and genetic diagnostic test exceptions
|
190 |
5.5.1 General rules applicable to both exceptions
|
192 |
5.5.1.1 Rule I: Mandatory character of the exceptions
|
192 |
5.5.1.2 Rule II: Duty to inform
|
193 |
5.5.1.3 Rule III: Guarantee of access to biological materials
|
193 |
5.5.1.4 Rule IV: Prohibition of reach-through patent claims and contractual clauses
|
193 |
5.5.1.5 Rule V: Establishment of a patent clearing house
|
195 |
5.5.1.6 Rule VI: De-bureaucratization of the procedures for granting compulsory licenses
|
197 |
5.5.1.6.1 Compulsory licensing for unique research tools
|
199 |
5.5.1.6.2 Compulsory licensing of blocking patents
|
200 |
5.5.2 R&D exception – first component: uses focused on generating knowledge on the subject matter of the patent and developing new innovations
|
201 |
5.5.3 R&D exception – second component: scientific and humanitarian uses
|
204 |
5.5.4 R&D exception – third component: dual inventions, when used as research tools
|
205 |
5.5.4.1 Differential treatment and graduated rates
|
207 |
5.5.5 R&D exception – fourth component: unique research tools
|
209 |
5.6 Assessment of the lawfulness of the R&D exception
|
211 |
5.6.1 First step: assessment of the limited character of the exception
|
211 |
5.6.2 Second step: assessment of the reasonableness of the interference caused by the exception
|
212 |
5.6.2.1 Proposals of exceptions governed by the TRIPS compulsory licensing system
|
214 |
5.6.2.2 Proposals based on the “fair use” defense
|
216 |
5.6.2.3 Proposals of sui generis patent exceptions
|
219 |
5.6.2.3.1 Janice Mueller’s proposal
|
219 |
5.6.2.3.2 Rochelle Dreyfuss’s proposal
|
221 |
5.6.2.3.3 Rebecca Eisenberg's proposal
|
223 |
5.6.2.4 Conclusions on the proposals examined
|
225 |
5.6.3 Third step: assessment of the reasonableness of the degree of harm caused by the R&D exception
|
226 |
5.7 The genetic diagnostic test exception and its functioning
|
227 |
5.8 Assessment of the lawfulness of the genetic diagnostic test exception in the light of art. 30 TRIPS
|
231 |
5.8.1 First step: assessment of the limited character of the exception
|
231 |
5.8.2 Second step: assessment of the reasonableness of the interference caused by the exception
|
233 |
5.8.2.1 Proposal of Lynn Rivers
|
233 |
5.8.2.2 Proposals based on a compulsory licensing scheme
|
234 |
5.8.3 Third step: assessment of the reasonableness of the prejudice caused by the exception
|
235 |
6 Trademarks and the parody and criticism exception
|
237 |
6.1 Introduction
|
237 |
6.2 Some cases involving conflicts between the exclusive right conferred by trademarks and freedom of expression
|
240 |
6.2.1 Laugh It Off case
|
240 |
6.2.2 Areva case
|
243 |
6.2.3 Esso case
|
245 |
6.2.4 Danone case
|
247 |
6.2.5 “Guaraná Power” case
|
248 |
6.2.6 Brazilian Olympic Committee case
|
250 |
6.2.7 Tata Sons case
|
252 |
6.2.8 Lessons to be drawn from the cases
|
255 |
6.3 Proposal of a parody and criticism exception
|
258 |
6.3.1 Assessment of the legality of the parody and criticism exception
|
262 |
7 Industrial designs and the repair exception
|
266 |
7.1 Introduction
|
266 |
7.2 ANFAPE case
|
268 |
7.2.1 SDE’s ruling
|
271 |
7.2.2 Efforts to reverse SDE’s ruling
|
276 |
7.3 European proposal for a repair exception
|
282 |
7.4 Assessment of the lawfulness of the European repair exception
|
287 |
7.4.1 First step
|
287 |
7.4.2 Second step
|
288 |
7.4.3 Third step
|
290 |
8 Copyright and the educational exception for underprivileged students and researchers
|
292 |
8.1 Introduction
|
292 |
8.2 The broadening of exclusive rights and the Brazilian Copyright Act of 1998
|
297 |
8.2.1 The cumbersome Brazilian private copying exception
|
301 |
8.2.2 The response of the Brazilian government
|
309 |
8.3 Proposal for an educational exception for underprivileged students and researchers
|
312 |
8.3.1 Assessment of the legality of the proposed educational exception
|
315 |
8.3.1.1 Assessment of the special character of the exception
|
315 |
8.3.1.2 Assessment of the ability of the exception to conflict with the normal exploitation of the affected works
|
318 |
8.3.1.3 Assessment of the unreasonable character of the prejudice caused by the exception to the legitimate interests of copyright holders
|
319 |
Concluding remarks on Part II
|
320 |
Final remarks
|
326 |
Bibliography
|
330 |
Index
|
351 |