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	<channel><title><![CDATA[Latest Publisher Reports]]></title><atom:link href="http://www.researchmoz.com/publisher" rel="self" type="application/rss+xml" />
	<link>http://www.researchmoz.com</link>
	<description><![CDATA[Latest Publisher Reports]]></description>
	<lastBuildDate>Wed, 18 Jul 2012 12:20:54 +0000</lastBuildDate>
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	<generator>http://wordpress.org/?v=3.3.1</generator><item><title>Risk Sharing and Other Forms of Managed Entry Agreements for Medicines, Worldwide</title><link>http://www.researchmoz.com/risk-sharing-and-other-forms-of-managed-entry-agreements-for-medicines-worldwide-report.html</link><comments>http://www.researchmoz.com/risk-sharing-and-other-forms-of-managed-entry-agreements-for-medicines-worldwide-report.html#comments</comments><pubDate>Fri, 01 Feb 2013 00:00:00 -0600</pubDate><dc:creator>admin</dc:creator><guid isPermaLink='false'>http://www.researchmoz.com/risk-sharing-and-other-forms-of-managed-entry-agreements-for-medicines-worldwide-report.html</guid><description><![CDATA[
Managed entry agreements apply to an increasing number of new, innovative drugs in a growing number of markets. They are designed to share the risk between the manufacturer and the payer, consequent on uncertainties - usually at launch - about the product&rsquo;s value (clinical- and cost-effectiveness), budget impact and/or utilisation to optimise performance, whilst at the same time allowing patient access. For many products considered costly they are almost essential to achieve reimbursement where health technology assessment is applied.

Risk Sharing and Other Forms of Managed Entry Agreements for Medicines, Worldwide covers all the main types of agreements (finance-based, outcome- or performance-based, and compliance-based) and their many variants in all countries that employ them. The confusing taxonomy associated with the topic (e.g. price/volume deals, budget impact schemes, cost capping, cost sharing, coverage with evidence development, money back guarantees, conditional r <br><br>Original Post <a href=http://www.researchmoz.com/risk-sharing-and-other-forms-of-managed-entry-agreements-for-medicines-worldwide-report.html>Risk Sharing and Other Forms of Managed Entry Agreements for Medicines, Worldwide</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></description><content:encoded><![CDATA[
Managed entry agreements apply to an increasing number of new, innovative drugs in a growing number of markets. They are designed to share the risk between the manufacturer and the payer, consequent on uncertainties - usually at launch - about the product&rsquo;s value (clinical- and cost-effectiveness), budget impact and/or utilisation to optimise performance, whilst at the same time allowing patient access. For many products considered costly they are almost essential to achieve reimbursement where health technology assessment is applied.

Risk Sharing and Other Forms of Managed Entry Agreements for Medicines, Worldwide covers all the main types of agreements (finance-based, outcome- or performance-based, and compliance-based) and their many variants in all countries that employ them. The confusing taxonomy associated with the topic (e.g. price/volume deals, budget impact schemes, cost capping, cost sharing, coverage with evidence development, money back guarantees, conditional r <br><br>Original Post <a href=http://www.researchmoz.com/risk-sharing-and-other-forms-of-managed-entry-agreements-for-medicines-worldwide-report.html>Risk Sharing and Other Forms of Managed Entry Agreements for Medicines, Worldwide</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></content:encoded><wfw:commentRss>http://www.researchmoz.com/risk-sharing-and-other-forms-of-managed-entry-agreements-for-medicines-worldwide-report.html/feed</wfw:commentRss><slash:comments>0</slash:comments>	</item><item><title>Pharmaceutical Pricing &amp; Distribution in Japan, 2012 Update</title><link>http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2012-update-report.html</link><comments>http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2012-update-report.html#comments</comments><pubDate>Wed, 13 Jun 2012 00:00:00 -0500</pubDate><dc:creator>admin</dc:creator><guid isPermaLink='false'>http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2012-update-report.html</guid><description><![CDATA[
No serious pharmaceutical company can afford to ignore Japan, a $120 billion market, the&nbsp;second-largest in the world. It remains a tough and highly competitive market to crack,&nbsp;however, with the environment for developing and marketing medicines dominated by price.&nbsp;

No new brand can be introduced without a yakka (reimbursement price) set by the&nbsp;
government. Innovative drugs receive price premiums while others are capped at the price of &nbsp;older entrants. Discounting to the trade is inescapable, but is punished by downward price&nbsp;revisions on a scale and frequency unseen elsewhere. &nbsp;Big selling brands are repriced.

Distribution is inherently linked to the pricing process and is particularly opaque to outsiders&nbsp;This latest, fully-updated and enlarged version of the critically-acclaimed best-seller includes&nbsp;

all the essentials you need to optimise market access and life cycle management. &nbsp;
&nbsp;&nbsp;


New drug pricing and p <br><br>Original Post <a href=http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2012-update-report.html>Pharmaceutical Pricing &amp; Distribution in Japan, 2012 Update</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></description><content:encoded><![CDATA[
No serious pharmaceutical company can afford to ignore Japan, a $120 billion market, the&nbsp;second-largest in the world. It remains a tough and highly competitive market to crack,&nbsp;however, with the environment for developing and marketing medicines dominated by price.&nbsp;

No new brand can be introduced without a yakka (reimbursement price) set by the&nbsp;
government. Innovative drugs receive price premiums while others are capped at the price of &nbsp;older entrants. Discounting to the trade is inescapable, but is punished by downward price&nbsp;revisions on a scale and frequency unseen elsewhere. &nbsp;Big selling brands are repriced.

Distribution is inherently linked to the pricing process and is particularly opaque to outsiders&nbsp;This latest, fully-updated and enlarged version of the critically-acclaimed best-seller includes&nbsp;

all the essentials you need to optimise market access and life cycle management. &nbsp;
&nbsp;&nbsp;


New drug pricing and p <br><br>Original Post <a href=http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2012-update-report.html>Pharmaceutical Pricing &amp; Distribution in Japan, 2012 Update</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></content:encoded><wfw:commentRss>http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2012-update-report.html/feed</wfw:commentRss><slash:comments>0</slash:comments>	</item><item><title>Biosimilars: Current Situation &amp; Future Prospects, Worldwide</title><link>http://www.researchmoz.com/biosimilars-current-situation-and-future-prospects-worldwide-report.html</link><comments>http://www.researchmoz.com/biosimilars-current-situation-and-future-prospects-worldwide-report.html#comments</comments><pubDate>Thu, 01 Mar 2012 00:00:00 -0600</pubDate><dc:creator>admin</dc:creator><guid isPermaLink='false'>http://www.researchmoz.com/biosimilars-current-situation-and-future-prospects-worldwide-report.html</guid><description><![CDATA[
The engine of the biosimilar sector is the  same as with small molecule drugs, patent expiry. On this basis,  prospects for biosimilars look good, with the vast majority of leading  originator brands in the global biologics market expected to lose some  degree of protection by 2019. All major countries now make provision for  an abbreviated biosimilar development and regulatory pathway. Funds are  flowing into the sector and many new partnership agreements signed.  Everything in the biosimilar garden might look rosy, but what is the  reality?  Biosimilar sales of $16+ billion were forecast in the EU and US alone  for 2011.This estimate turned out to be 50-times too high. Does  publication of the long-awaited guidance on the US Biologics Price  Competition and Innovation Act mean a new dawn for biosimilars, or  another false one?  Written with the understandable detail and  objectivity you need, Biosimilars: Current Situation &amp; Future  Prospects, Worldwide provides the answers, in <br><br>Original Post <a href=http://www.researchmoz.com/biosimilars-current-situation-and-future-prospects-worldwide-report.html>Biosimilars: Current Situation &amp; Future Prospects, Worldwide</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></description><content:encoded><![CDATA[
The engine of the biosimilar sector is the  same as with small molecule drugs, patent expiry. On this basis,  prospects for biosimilars look good, with the vast majority of leading  originator brands in the global biologics market expected to lose some  degree of protection by 2019. All major countries now make provision for  an abbreviated biosimilar development and regulatory pathway. Funds are  flowing into the sector and many new partnership agreements signed.  Everything in the biosimilar garden might look rosy, but what is the  reality?  Biosimilar sales of $16+ billion were forecast in the EU and US alone  for 2011.This estimate turned out to be 50-times too high. Does  publication of the long-awaited guidance on the US Biologics Price  Competition and Innovation Act mean a new dawn for biosimilars, or  another false one?  Written with the understandable detail and  objectivity you need, Biosimilars: Current Situation &amp; Future  Prospects, Worldwide provides the answers, in <br><br>Original Post <a href=http://www.researchmoz.com/biosimilars-current-situation-and-future-prospects-worldwide-report.html>Biosimilars: Current Situation &amp; Future Prospects, Worldwide</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></content:encoded><wfw:commentRss>http://www.researchmoz.com/biosimilars-current-situation-and-future-prospects-worldwide-report.html/feed</wfw:commentRss><slash:comments>0</slash:comments>	</item><item><title>Pharmaceutical Pricing &amp; Distribution in Japan, 2010 Update</title><link>http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2010-update-report.html</link><comments>http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2010-update-report.html#comments</comments><pubDate>Sat, 01 Oct 2011 00:00:00 -0500</pubDate><dc:creator>admin</dc:creator><guid isPermaLink='false'>http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2010-update-report.html</guid><description><![CDATA[
The author&rsquo;s 2008 major title  &lsquo;Pharmaceutical Pricing &amp; Distribution in Japan&rsquo; was described by  PhRMA Japan as &lsquo;a superb report&hellip;to understand Japan there is nothing  better&rsquo;. His new report packs all the essentials needed to optimise  market access and life cycle management into 60 pages and offers  tremendous value. Completely updated, it explains all the latest changes  to the NHI pricing rules, including the important new price premium for  developing new drugs/new indications. 

New drug pricing and price revision processes made completely clear, with all formulae used and many up-to-date examples
Incorporates all pricing rule changes coming into effect from April 2010 with forecast of further reforms in FY 2012
Written by an acknowledged expert on the Japanese market with 23 years&rsquo; experience 
Fully researched through interviews conducted in Tokyo with  industry experts, government officials and local consultants. Lots of  in <br><br>Original Post <a href=http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2010-update-report.html>Pharmaceutical Pricing &amp; Distribution in Japan, 2010 Update</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></description><content:encoded><![CDATA[
The author&rsquo;s 2008 major title  &lsquo;Pharmaceutical Pricing &amp; Distribution in Japan&rsquo; was described by  PhRMA Japan as &lsquo;a superb report&hellip;to understand Japan there is nothing  better&rsquo;. His new report packs all the essentials needed to optimise  market access and life cycle management into 60 pages and offers  tremendous value. Completely updated, it explains all the latest changes  to the NHI pricing rules, including the important new price premium for  developing new drugs/new indications. 

New drug pricing and price revision processes made completely clear, with all formulae used and many up-to-date examples
Incorporates all pricing rule changes coming into effect from April 2010 with forecast of further reforms in FY 2012
Written by an acknowledged expert on the Japanese market with 23 years&rsquo; experience 
Fully researched through interviews conducted in Tokyo with  industry experts, government officials and local consultants. Lots of  in <br><br>Original Post <a href=http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2010-update-report.html>Pharmaceutical Pricing &amp; Distribution in Japan, 2010 Update</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></content:encoded><wfw:commentRss>http://www.researchmoz.com/pharmaceutical-pricing-and-distribution-in-japan-2010-update-report.html/feed</wfw:commentRss><slash:comments>0</slash:comments>	</item><item><title>Orphan Drugs in Europe: Pricing, Reimbursement, Funding &amp; Market Access Issues, 2011 Edition</title><link>http://www.researchmoz.com/orphan-drugs-in-europe-pricing-reimbursement-funding-and-market-access-issues-2011-edition-report.html</link><comments>http://www.researchmoz.com/orphan-drugs-in-europe-pricing-reimbursement-funding-and-market-access-issues-2011-edition-report.html#comments</comments><pubDate>Wed, 01 Jun 2011 00:00:00 -0500</pubDate><dc:creator>admin</dc:creator><guid isPermaLink='false'>http://www.researchmoz.com/orphan-drugs-in-europe-pricing-reimbursement-funding-and-market-access-issues-2011-edition-report.html</guid><description><![CDATA[The cost of treating rare disease in an age when austerity measures are hitting total healthcare funding across Europe is a highly controversial, even emotive subject. There is a clear and pressing clinical need, a strong patient voice and the treatments themselves sometimes offer the only hope. But is this enough to assure premium prices and special status in an era of budget limitations, and growing demands for evidence of clinical and cost effectiveness?&nbsp;

The orphan drug Regulation 141/2000, resulting in 724 designated products and 62 marketing approvals in the first 10 years, has certainly been one of the most successful legislative measures by the EU. Encouraging development and accelerating regulatory approval are very important, but alone do not ensure orphan drugs are actually available for use. Rare disease patients need timely access to therapies that are fully funded by social health insurance/national health services. Hurdles are found at national, regional and loca <br><br>Original Post <a href=http://www.researchmoz.com/orphan-drugs-in-europe-pricing-reimbursement-funding-and-market-access-issues-2011-edition-report.html>Orphan Drugs in Europe: Pricing, Reimbursement, Funding &amp; Market Access Issues, 2011 Edition</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></description><content:encoded><![CDATA[The cost of treating rare disease in an age when austerity measures are hitting total healthcare funding across Europe is a highly controversial, even emotive subject. There is a clear and pressing clinical need, a strong patient voice and the treatments themselves sometimes offer the only hope. But is this enough to assure premium prices and special status in an era of budget limitations, and growing demands for evidence of clinical and cost effectiveness?&nbsp;

The orphan drug Regulation 141/2000, resulting in 724 designated products and 62 marketing approvals in the first 10 years, has certainly been one of the most successful legislative measures by the EU. Encouraging development and accelerating regulatory approval are very important, but alone do not ensure orphan drugs are actually available for use. Rare disease patients need timely access to therapies that are fully funded by social health insurance/national health services. Hurdles are found at national, regional and loca <br><br>Original Post <a href=http://www.researchmoz.com/orphan-drugs-in-europe-pricing-reimbursement-funding-and-market-access-issues-2011-edition-report.html>Orphan Drugs in Europe: Pricing, Reimbursement, Funding &amp; Market Access Issues, 2011 Edition</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></content:encoded><wfw:commentRss>http://www.researchmoz.com/orphan-drugs-in-europe-pricing-reimbursement-funding-and-market-access-issues-2011-edition-report.html/feed</wfw:commentRss><slash:comments>0</slash:comments>	</item><item><title>Market Access Korea: Breaking into the Developed World&#039;s Fastest Growing Pharmaceutical Market</title><link>http://www.researchmoz.com/market-access-korea-breaking-into-the-developed-worlds-fastest-growing-pharmaceutical-market-report.html</link><comments>http://www.researchmoz.com/market-access-korea-breaking-into-the-developed-worlds-fastest-growing-pharmaceutical-market-report.html#comments</comments><pubDate>Mon, 01 Nov 2010 00:00:00 -0500</pubDate><dc:creator>admin</dc:creator><guid isPermaLink='false'>http://www.researchmoz.com/market-access-korea-breaking-into-the-developed-worlds-fastest-growing-pharmaceutical-market-report.html</guid><description><![CDATA[

South Korea as a country has been an economic success story and the origin of much cutting edge technology, but its pharmaceutical market can now also be given &lsquo;Asian tiger&rsquo; status. The past four years have seen total sales growth of 15.6%, 13.5%, 12.4% and 13.8% respectively. IMS forecasts CAGR of 6.5% from 2010 through 2015, making Korea the fastest growing developed market for medicines in the world.

Currently ranked fourth in Asia-Pacific - after Japan, China and India, but ahead of Australia - drug sales at manufacturer selling prices are the equivalent of USD 11 billion. If you consider that foreign innovative products did not gain access to the reimbursement system until late 1999 it is remarkable that multinational companies today hold half of the top-10 sales rankings with prescription products and in total have a 40% market share.&nbsp;

Modern-day Korea is trying hard to shake off its reputation for lack of transparency in reimbursement decisions and unf <br><br>Original Post <a href=http://www.researchmoz.com/market-access-korea-breaking-into-the-developed-worlds-fastest-growing-pharmaceutical-market-report.html>Market Access Korea: Breaking into the Developed World&#039;s Fastest Growing Pharmaceutical Market</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></description><content:encoded><![CDATA[

South Korea as a country has been an economic success story and the origin of much cutting edge technology, but its pharmaceutical market can now also be given &lsquo;Asian tiger&rsquo; status. The past four years have seen total sales growth of 15.6%, 13.5%, 12.4% and 13.8% respectively. IMS forecasts CAGR of 6.5% from 2010 through 2015, making Korea the fastest growing developed market for medicines in the world.

Currently ranked fourth in Asia-Pacific - after Japan, China and India, but ahead of Australia - drug sales at manufacturer selling prices are the equivalent of USD 11 billion. If you consider that foreign innovative products did not gain access to the reimbursement system until late 1999 it is remarkable that multinational companies today hold half of the top-10 sales rankings with prescription products and in total have a 40% market share.&nbsp;

Modern-day Korea is trying hard to shake off its reputation for lack of transparency in reimbursement decisions and unf <br><br>Original Post <a href=http://www.researchmoz.com/market-access-korea-breaking-into-the-developed-worlds-fastest-growing-pharmaceutical-market-report.html>Market Access Korea: Breaking into the Developed World&#039;s Fastest Growing Pharmaceutical Market</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></content:encoded><wfw:commentRss>http://www.researchmoz.com/market-access-korea-breaking-into-the-developed-worlds-fastest-growing-pharmaceutical-market-report.html/feed</wfw:commentRss><slash:comments>0</slash:comments>	</item><item><title>Orphan Drugs in Asia-Pacific: From Designation to Pricing, Funding &amp; Market Access</title><link>http://www.researchmoz.com/orphan-drugs-in-asia-pacific-from-designation-to-pricing-funding-and-market-access-report.html</link><comments>http://www.researchmoz.com/orphan-drugs-in-asia-pacific-from-designation-to-pricing-funding-and-market-access-report.html#comments</comments><pubDate>Mon, 01 Feb 2010 00:00:00 -0600</pubDate><dc:creator>admin</dc:creator><guid isPermaLink='false'>http://www.researchmoz.com/orphan-drugs-in-asia-pacific-from-designation-to-pricing-funding-and-market-access-report.html</guid><description><![CDATA[A major new report Orphan Drugs in Asia-Pacific: From designation to pricing, funding and market access focuses on five developed markets in the region: Japan, South Korea, Taiwan, Singapore and Australia. Each has passed specific measures to promote the development, registration and/or commercialisation of rare disease treatments. Singapore&rsquo;s Medicines (Orphan Drug) Exemption Order of 1991 was the first legislation anywhere to follow the US Orphan Drug Act, with the other four Asia-Pacific countries also implementing orphan-promoting measures ahead of the EU.&nbsp;

Rare diseases are collectively not that rare, indeed 6-10% of people will suffer from one at some point in life. Asia-Pacific contains nearly two-thirds of the world&rsquo;s population, and should offer great potential to companies developing orphan drugs. But clinical need alone does not mean that adequate money for diagnosis and treatment will be made available.&nbsp;

The report describes the processes for obt <br><br>Original Post <a href=http://www.researchmoz.com/orphan-drugs-in-asia-pacific-from-designation-to-pricing-funding-and-market-access-report.html>Orphan Drugs in Asia-Pacific: From Designation to Pricing, Funding &amp; Market Access</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></description><content:encoded><![CDATA[A major new report Orphan Drugs in Asia-Pacific: From designation to pricing, funding and market access focuses on five developed markets in the region: Japan, South Korea, Taiwan, Singapore and Australia. Each has passed specific measures to promote the development, registration and/or commercialisation of rare disease treatments. Singapore&rsquo;s Medicines (Orphan Drug) Exemption Order of 1991 was the first legislation anywhere to follow the US Orphan Drug Act, with the other four Asia-Pacific countries also implementing orphan-promoting measures ahead of the EU.&nbsp;

Rare diseases are collectively not that rare, indeed 6-10% of people will suffer from one at some point in life. Asia-Pacific contains nearly two-thirds of the world&rsquo;s population, and should offer great potential to companies developing orphan drugs. But clinical need alone does not mean that adequate money for diagnosis and treatment will be made available.&nbsp;

The report describes the processes for obt <br><br>Original Post <a href=http://www.researchmoz.com/orphan-drugs-in-asia-pacific-from-designation-to-pricing-funding-and-market-access-report.html>Orphan Drugs in Asia-Pacific: From Designation to Pricing, Funding &amp; Market Access</a> <br> source  <a href="http://www.researchmoz.com">Researchmoz</a>]]></content:encoded><wfw:commentRss>http://www.researchmoz.com/orphan-drugs-in-asia-pacific-from-designation-to-pricing-funding-and-market-access-report.html/feed</wfw:commentRss><slash:comments>0</slash:comments>	</item></channel></rss>