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documents
Ensuring incentives for innovation
and access to medicines
The balance struck in the Trans-Pacific Partnership
Agreement on intellectual property
(patent and regulatory data)
protection for pharmaceutical products
Rosine M. Plank-Brumback
Pharmaceutical Research and Manufacturers of America (PhRma)
Public Citizen's Global Access to Medicines
International Generic and Biosimilar Medicines Association (IGBA)
PhRMA Statement on the Transpacific Partnership Negotiations
TPP Transition Periods on Pharmaceutical Intellectual Property Rules: Bad
Rules Coming Soon in a TPP Country Near You
See
Working Session 10:
Principles to Foster Trade in Generic and Biosimilar Medicines
available at
—
inter alia
et al
inter alia
e.g.
e.g.
per se
United States Section 337 of the Tariff Act of 1930
Id
Id
Id
inter alia
inter
alia
ordre public
sui generis
•
•
•
e.g
Supra
Id.
Id.,
Id
see
inter alia
•
•
•
Supra
supra
pro tempore
see
Supra
BIO Statement on Data Exclusivity Provisions Within the Trans-Pacific Partnership
supra
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
Supra
•
•
inter alia
•
•
supra
•
•
•
•
•
inter alia
supra
•
•
•
•
See supra
Wall Street Journal
Wall Street Journal
supra
supra see supra
The SciTech Lawyer
supra supra
Id.
The Economist
See
The Economist
•
•
•
•
ordre public
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
inter alia
• Protocol
Amending the TRIPS Agreement, i.e.
•
•
e.g.
marketing approval granted in another territory
the first marketing approval relied on.”
US-Peru FTA i.e. a reasonable period of time
which shall normally mean 5 years.
Con excepción de patentes farmacéuticas
inter alia
et al
inter alia
Supra
See
The
Economist
available
on request at
et al
Table A.1
International applications filed under the Patent Cooperation Treaty (PCT) from TPP States
Canada
Chile
Mexico
Peru
United States
Total TPP
Table A.2
International applications filed under the PCT
from western hemisphere (OAS Member) States
Chile
Mexico
Peru
Total Latin America and Caribbean
Canada
United States
Total Western Hemisphere
Table A.3
Transition periods for implementing certain (TRIPS-Plus)
patent and data provisions for pharmaceutical products
under the TPPA
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