Loading…
BPCIA UPDATE: ENTROPY IS THE PRICE OF AN ORDERED FRAMEWORK
The pharmaceutical industry has often relied on patent law to protect its investments, recoup costs associated with research and development (e.g., clinical trials), and encourage innovation. Simultaneously, because of patent law's strong protections, a premium is added to drug prices--which li...
Saved in:
Published in: | Berkeley technology law journal 2019-04, Vol.33 (4), p.1277 |
---|---|
Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 4 |
container_start_page | 1277 |
container_title | Berkeley technology law journal |
container_volume | 33 |
creator | Kulathila, Rithika |
description | The pharmaceutical industry has often relied on patent law to protect its investments, recoup costs associated with research and development (e.g., clinical trials), and encourage innovation. Simultaneously, because of patent law's strong protections, a premium is added to drug prices--which limits accessibility and affordability to these life-saving therapies. In order to address this concern, Congress created the Hatch-Waxman Amendments in 1984 for small molecule drugs. The Act sought to balance incentives for the pharmaceutical industry as well as increase accessibility and affordability of life-saving drugs for patients. While the Supreme Court settled questions about remedies for statutory violations, the Court's interpretation of the timing of 180-day notice may have some unintended consequences. First, 180-day pre-licensure can lead to parties blindly litigating over controversies that may or may not fully crystallize. Second, by giving the biosimilar manufacturer flexibility on when it can provide 180-day notice, the biosimilar manufacturer may use notice to encourage pay-for-delay settlements. |
doi_str_mv | 10.15779/Z388P5V921 |
format | article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_2239628321</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2239628321</sourcerecordid><originalsourceid>FETCH-proquest_journals_22396283213</originalsourceid><addsrcrecordid>eNqNyrsOgjAYQOHGaCJeJl_gT5zRXrgUtgolECM0tWp0IQ44ECMK8v46-ABOZ_gOQguCV8T1_WB9YZwr9xhQMkAWZRzbju_QIbII5p7NOOFjNOm6GmNMMWEWCjcqygQcVCyMDEHmRhfqDNkeTCpB6SySUCQgcih0LLWMIdFiJ0-F3s7Q6Ha9d9X81ylaJtJEqf1sm1dfde-ybvr28aWSUhZ4lDNK2H_XBwNqNgg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2239628321</pqid></control><display><type>article</type><title>BPCIA UPDATE: ENTROPY IS THE PRICE OF AN ORDERED FRAMEWORK</title><source>International Bibliography of the Social Sciences (IBSS)</source><source>Nexis UK</source><source>JSTOR Archival Journals and Primary Sources Collection</source><source>BSC - Ebsco (Business Source Ultimate)</source><creator>Kulathila, Rithika</creator><creatorcontrib>Kulathila, Rithika</creatorcontrib><description>The pharmaceutical industry has often relied on patent law to protect its investments, recoup costs associated with research and development (e.g., clinical trials), and encourage innovation. Simultaneously, because of patent law's strong protections, a premium is added to drug prices--which limits accessibility and affordability to these life-saving therapies. In order to address this concern, Congress created the Hatch-Waxman Amendments in 1984 for small molecule drugs. The Act sought to balance incentives for the pharmaceutical industry as well as increase accessibility and affordability of life-saving drugs for patients. While the Supreme Court settled questions about remedies for statutory violations, the Court's interpretation of the timing of 180-day notice may have some unintended consequences. First, 180-day pre-licensure can lead to parties blindly litigating over controversies that may or may not fully crystallize. Second, by giving the biosimilar manufacturer flexibility on when it can provide 180-day notice, the biosimilar manufacturer may use notice to encourage pay-for-delay settlements.</description><identifier>ISSN: 1086-3818</identifier><identifier>EISSN: 2380-4742</identifier><identifier>DOI: 10.15779/Z388P5V921</identifier><language>eng</language><publisher>Berkeley: University of California, Boalt Hall School of Law</publisher><subject>Access ; Affordability ; Amendments ; Biological products ; Clinical research ; Clinical trials ; Drug prices ; Entropy ; Flexibility ; Incentives ; Innovations ; Investments ; Licensing ; Lifesaving ; Patent law ; Pharmaceutical industry ; Prices ; R&D ; Research & development ; Settlements & damages ; Supreme courts ; Violations</subject><ispartof>Berkeley technology law journal, 2019-04, Vol.33 (4), p.1277</ispartof><rights>Copyright University of California, Boalt Hall School of Law Apr 27, 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,33223</link.rule.ids></links><search><creatorcontrib>Kulathila, Rithika</creatorcontrib><title>BPCIA UPDATE: ENTROPY IS THE PRICE OF AN ORDERED FRAMEWORK</title><title>Berkeley technology law journal</title><description>The pharmaceutical industry has often relied on patent law to protect its investments, recoup costs associated with research and development (e.g., clinical trials), and encourage innovation. Simultaneously, because of patent law's strong protections, a premium is added to drug prices--which limits accessibility and affordability to these life-saving therapies. In order to address this concern, Congress created the Hatch-Waxman Amendments in 1984 for small molecule drugs. The Act sought to balance incentives for the pharmaceutical industry as well as increase accessibility and affordability of life-saving drugs for patients. While the Supreme Court settled questions about remedies for statutory violations, the Court's interpretation of the timing of 180-day notice may have some unintended consequences. First, 180-day pre-licensure can lead to parties blindly litigating over controversies that may or may not fully crystallize. Second, by giving the biosimilar manufacturer flexibility on when it can provide 180-day notice, the biosimilar manufacturer may use notice to encourage pay-for-delay settlements.</description><subject>Access</subject><subject>Affordability</subject><subject>Amendments</subject><subject>Biological products</subject><subject>Clinical research</subject><subject>Clinical trials</subject><subject>Drug prices</subject><subject>Entropy</subject><subject>Flexibility</subject><subject>Incentives</subject><subject>Innovations</subject><subject>Investments</subject><subject>Licensing</subject><subject>Lifesaving</subject><subject>Patent law</subject><subject>Pharmaceutical industry</subject><subject>Prices</subject><subject>R&D</subject><subject>Research & development</subject><subject>Settlements & damages</subject><subject>Supreme courts</subject><subject>Violations</subject><issn>1086-3818</issn><issn>2380-4742</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>8BJ</sourceid><recordid>eNqNyrsOgjAYQOHGaCJeJl_gT5zRXrgUtgolECM0tWp0IQ44ECMK8v46-ABOZ_gOQguCV8T1_WB9YZwr9xhQMkAWZRzbju_QIbII5p7NOOFjNOm6GmNMMWEWCjcqygQcVCyMDEHmRhfqDNkeTCpB6SySUCQgcih0LLWMIdFiJ0-F3s7Q6Ha9d9X81ylaJtJEqf1sm1dfde-ybvr28aWSUhZ4lDNK2H_XBwNqNgg</recordid><startdate>20190427</startdate><enddate>20190427</enddate><creator>Kulathila, Rithika</creator><general>University of California, Boalt Hall School of Law</general><scope>8BJ</scope><scope>FQK</scope><scope>JBE</scope></search><sort><creationdate>20190427</creationdate><title>BPCIA UPDATE: ENTROPY IS THE PRICE OF AN ORDERED FRAMEWORK</title><author>Kulathila, Rithika</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_22396283213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Access</topic><topic>Affordability</topic><topic>Amendments</topic><topic>Biological products</topic><topic>Clinical research</topic><topic>Clinical trials</topic><topic>Drug prices</topic><topic>Entropy</topic><topic>Flexibility</topic><topic>Incentives</topic><topic>Innovations</topic><topic>Investments</topic><topic>Licensing</topic><topic>Lifesaving</topic><topic>Patent law</topic><topic>Pharmaceutical industry</topic><topic>Prices</topic><topic>R&D</topic><topic>Research & development</topic><topic>Settlements & damages</topic><topic>Supreme courts</topic><topic>Violations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kulathila, Rithika</creatorcontrib><collection>International Bibliography of the Social Sciences (IBSS)</collection><collection>International Bibliography of the Social Sciences</collection><collection>International Bibliography of the Social Sciences</collection><jtitle>Berkeley technology law journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kulathila, Rithika</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BPCIA UPDATE: ENTROPY IS THE PRICE OF AN ORDERED FRAMEWORK</atitle><jtitle>Berkeley technology law journal</jtitle><date>2019-04-27</date><risdate>2019</risdate><volume>33</volume><issue>4</issue><spage>1277</spage><pages>1277-</pages><issn>1086-3818</issn><eissn>2380-4742</eissn><abstract>The pharmaceutical industry has often relied on patent law to protect its investments, recoup costs associated with research and development (e.g., clinical trials), and encourage innovation. Simultaneously, because of patent law's strong protections, a premium is added to drug prices--which limits accessibility and affordability to these life-saving therapies. In order to address this concern, Congress created the Hatch-Waxman Amendments in 1984 for small molecule drugs. The Act sought to balance incentives for the pharmaceutical industry as well as increase accessibility and affordability of life-saving drugs for patients. While the Supreme Court settled questions about remedies for statutory violations, the Court's interpretation of the timing of 180-day notice may have some unintended consequences. First, 180-day pre-licensure can lead to parties blindly litigating over controversies that may or may not fully crystallize. Second, by giving the biosimilar manufacturer flexibility on when it can provide 180-day notice, the biosimilar manufacturer may use notice to encourage pay-for-delay settlements.</abstract><cop>Berkeley</cop><pub>University of California, Boalt Hall School of Law</pub><doi>10.15779/Z388P5V921</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1086-3818 |
ispartof | Berkeley technology law journal, 2019-04, Vol.33 (4), p.1277 |
issn | 1086-3818 2380-4742 |
language | eng |
recordid | cdi_proquest_journals_2239628321 |
source | International Bibliography of the Social Sciences (IBSS); Nexis UK; JSTOR Archival Journals and Primary Sources Collection; BSC - Ebsco (Business Source Ultimate) |
subjects | Access Affordability Amendments Biological products Clinical research Clinical trials Drug prices Entropy Flexibility Incentives Innovations Investments Licensing Lifesaving Patent law Pharmaceutical industry Prices R&D Research & development Settlements & damages Supreme courts Violations |
title | BPCIA UPDATE: ENTROPY IS THE PRICE OF AN ORDERED FRAMEWORK |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T19%3A02%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=BPCIA%20UPDATE:%20ENTROPY%20IS%20THE%20PRICE%20OF%20AN%20ORDERED%20FRAMEWORK&rft.jtitle=Berkeley%20technology%20law%20journal&rft.au=Kulathila,%20Rithika&rft.date=2019-04-27&rft.volume=33&rft.issue=4&rft.spage=1277&rft.pages=1277-&rft.issn=1086-3818&rft.eissn=2380-4742&rft_id=info:doi/10.15779/Z388P5V921&rft_dat=%3Cproquest%3E2239628321%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_journals_22396283213%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2239628321&rft_id=info:pmid/&rfr_iscdi=true |