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MGMT 470 Case Study The Rise of India's Drug Industry
Case Study The Rise of India's Drug IndustryHow might US pharmaceutical companies and US consumers benefit from the rise of the Indian pharmaceutical industry?2. Who might have lost out as a result of the recent rise of the Indian pharmaceutical industry?3. Do the benefits from trade with the Indian pharmaceutical sector outweigh the losses?4. What international trade theory (or theories) best explain the rise of the India as a major exporter of pharmaceuticals?
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***** **** subsectors ***** **** be ******** later ** These ********** *** the patented generic *** over-the-counter ***** **************** on International ***** ***** ** the generator ** drugs *** *** ******** ** the ********* *** *** ** ***** ***** *** *** ********* ************ ******* pharma ********* **** ***** ***** center ** India **** **** aspect ***** has *** got *** ****** ** ****** ** original ********* ***** ********* into ****** ***** ** pharma ****** ** Company is not ******* ** ****** its ***** to participating ******* ****** *** ** the ***** in ***** ********** *** ** ******** ** *** ******** ***** **** **** ** approved ** the *** *** **** *** **** Administration *** ** *** is ****** ******** ** one ** the **** developed ********** ******** ** the ***** As * ****** of **** ** FDA ******* ********** *** **** as * ********* ** **** ******* countries ******* **** ******* ** the ** *** **** ***** repercussions ** * product’s ********** ********* ******** elseAlthough the *** ** known for some ** *** strict ******** *** ** the ****** ****** ****** ********** **** competitors elsewhere *** *** ******* ** ** is the ********* ** ****************** *********** *** ************ drugs **** ** ********* ****** *** resulted ** ********* ******** ** even **** ******* **** in the ** with **** ******* **** to influence ********* ******* *** ***** that *** * strong ********* on *** ****** ** ******** In ***** ** ********* ********* ********** ****** ******* the US operating environment ** ********** considerable ****** *** ******** ** ****** **** ** ********** ******* drugs *** universal ********** **** have * major ****** ** *** ****** ** *** ** **** *************** *** to demonstrate the **** ***** ** the ** market is ** ********* *** value ** *** ***** ***** ************** ******* Using personal ****** **** **** *** Bureau ** ******** Analysis a report **** Business ******* International ******** several ** ****** with ***** *********** in ******** *********** applied to ***** countries *** example *** ***** ** ******* *** $1927bn) ******** * ******* ***** ** ********* to ****** ********* This can **** ** **** ** comparisons ******* Russia *** $1792bn) *** ******** *** ******** ***** (US ******** and ************ *** ******** *** ****** (US $1174bn) *** New ****** ********* **** ****** ***** * **** **** ** *** ***** *** potential of *** US ****** ** *** ***************** ********** **************** is extremely ********* ** *** ************** industry ********* ******* ** *** ********** *** ** ******* *** ************ ******** ****** that the companies *** ****** ******* ** *** which ******* *** **** *********** **** *** ********* make in ******** *** *********** The ***** ************** ******** ** ****** ********* and the ********** controls *** ****** ** * ***** ****** ** **** ***** *** ************ These *********** have ** impact on *** ****** margins *** ******** *** *********** ******* ** both ******** *** ******* ************ it ** ******* ** **** ** how *********** in **** industry ******* what changes **** made **** *** ***** *** *** ***** ******* ******** the ******** *** main ********** body ** ***** ** the Central **** ******** ******* ************ ******* ***** *** Ministry of ****** and ****** ******* ***** ** ******** **** by *** Drug Controller-General ** ***** ****** *** ** ** ****** of ******** of licenses for ***** ** **** *** Central *** state ****** ***** introduced the ******* patent regime ** ********** with the TRIPS agreement ** January **** **** ** ********* ** *** ****** ****** ******** ** ********** ************* *** ** recent legislation *** ****** updates ************* ***** should ****** to **** ************* practices ***** ******** ** ******** * of *** ***** and ********* *** ************* ***** are ******** to comply with *** *** *** ************* ********* ** ********** The National ************** Pricing Authority ****** is *********** for ****** *** controlling the prices ** ** bulk ***** *** formulations under the Essential *********** ****** ******* ******* approved *** ********* ** *** ******* **** ********* ***** ** ******* ******* proposed organizational structure ** the *** ** to be ********* ** the ***** *** ****** ********* **** ** the ************** ******** **** ** a nodal ****** in *** ******* related to *** ****** ** *************** In ***** to **** ******** attention ** day-to-day ******** ***** ** the ********* *** **** ********* **** ******* ********************** *** *** Missions ****** *** **** **** ******** *********** **** ** export *** ****** ** pharmaceuticals ** *** ******* *** ******** ************ ****** *********** on ********** *** ********** ***** *** pharmaceutical exports *** **** *** been ********* with *** ************ ** ******** *** ********* on ********* quality control ************ *** of important countries ** as ** ******* domestic ********* *** exporting their ******** It communicates **** *** ******** ****** ** ******* *********** ******* ** ************** ******** ** ***** ********* **** as ****** ** the ************** ******** ******* of ************* ********** for ********* ** pharmaceutical ********* as **** as ************ *** ********* ******* of ************** ****** **** *********** ** local ********** *********** **** details ** ****** **** system health ********** *** ********* disease ******* ******* of ******* ** pharmaceuticals of ***** ********* ******* of joint venture ***** *** *************** operating ** these countries *** ** provides commercially useful *********** to *** ****************** *** ******** ************** ********** REGULATIONThe ******* ******* Direct ********** ****** ** the Government ** ***** ********** FDI ** ** *** *** cent ** the case ** bulk ***** ***** intermediates *** ******************* ***** ******** ** *** use ** *********** *** *********** would be ******* ***** *** automatic route *** ***** 75 *** cent *** manufacturing of bulk ***** **** ** ********** ** *** ********** ** **** ** **** ***** *** manufacture of **** ***** **** ***** stages *** ***** ************* and **** ***** ******** by *** *** ** *********** DNA ********** ** well as *** ******** *********** ******** ************ ******** ** ******** ************* **** ***** stagePharmaceutical ************ ******** RightsThe ********** ** ************ property ** ***** ** **** *********** at all ****** - ********* ************** and ******** The Agreement ** ***** Related ******* of ************ ******** ****** ******* **** **** force ** 01 ******* 1995 ** **** **** minimum ********* *** ********** *** *********** ** intellectual ******** rights ** member countries ***** *** ******** ** ******* *** effective *** adequate ********** of ************ ******** **** * **** ** reducing *********** *** *********** ** international ********** ** * ********** country *** * ********** ****** ** five ***** ***** ****** **** ** January 1995) ** ***** ** ******* 2000 ** ***** *** ********** ** the ********* ******* in **** *** changes ** ***** and ********** ********* ************* of ***** **** for ************** and ************* ** trade-marks ************ systems *** a comprehensive review ** *** ***** and *********** Marks *** **** *** **** *** * **** to repeal *** replace *** **** *** *** ***** been ****** ** ********** *** ******** ** *** ******* ** 30121999 This Act not only makes ***** ***** *** ***** ************* *** also ********** ** with international ******* and practicesSome *** Features ** *** ****** ******* Act of 2005 *************** of ******* ******* *** ***** ********* *** ***** ********* products ** ******** ************ Patent term made 20 ***** **** *** **** ** ********** of *** ******** **************** ********* *********** ** patent ************ after ** ****** ** *** ******** date ********** **** for ***** publication on ********** Creation of an appellate ***** *** ********** *** *********** ** **** ***** relevant ** the ************** ******** including ********* **** *** invention *** ************** ************* Reduction ** ****** ** ***** ***** price control ** ** as against 74 100 *** **** ******* ********** automatically permitted; ********* ******** for Foreign ********** ************* *********** ** ********** licensing *** **** drugs ************* *** formulationsPOLICY *********** AND ****** MEASURES 2009-10 ****** *********** ******* *** ******* **** **** ** *** **** ** * *** cent ** ******* of ****** *********** ***** *** ***** **** ***** *** ******** ******** **** ** breast cancer ********* ********* ********* etc ******* **** *** **** reduced from 75 *** **** to * *** cent ** *** ********* *********** devices **** ** *** ********* ** ***** ********** These ******* are *** ***** ****** **** ****** **** *** ************** **** ***** ******* *** government *** approved the ***** *** ******** (Amendment) **** 2008 ***** ***** **** ******** *** **** *** ************ **** five years to ** ***** 10 years ***** *** ****** ** ******** and raises *** **** **** ** ***** ** Rs ******** or ***** times the value ** the drug *********** *** manufacturers of ******** *** *********** ******** *** DCGI *** made *** ************ ** *** ******** ****** ********** *** ****** ********* ***** **** ** 2009 ******* the registration ** clinical ****** by ******* institutions *** companies *** ********* *** **** has ************ ******** of the ******* *********** for **** ************** products *** ***** ************** Regulatory InfrastructureThe first ***** that *** ******* looking at ********* * patented ******* ** * *** ****** ***** ** is ** ******** *** regulatory infrastructure of that ******* ** ensure **** *** intellectual ******** ** ************** protected *** ************ ** ******* ******* in ***** in 2005 *** opened up *** ****** for ****** launches However ******* companies are still **** ** India’s ** and ********** system *** ******* ** ***** ** ******* ******************** to ******* ************ the ****** ** ********* ***** ** *** domestic ****** *** been relatively **** Between January **** *** ***** **** **** ** patented ******** **** ******** ** ***** ** * ********* **** *** ******** the ****** ************** ********** ** regulatory ********* *** ***** ambiguities ********** ** ******* including exclusivity *** ********* *** ********** ********** ** ********* ******** to the ** regulatory infrastructure **** ******** *** ******* ********* feel the **** ** have * centralized regulatory **** This *** ******* *** ******* ** ******* the approvals *** ********** for * drug launchReferencesBhaumik * * ********* N & Pal * ****** **** ********* ********* of *************** ***** ****** their ******* FDI? The **** ** *** ****** ********** and ************** ************** ** International ******** ************ 437-450Fink * ********* ******** patent ********** in ***** ***** affect *** behavior ** ************* ************** industries ***** **** Development ******** ***** *********** * (2007)The ********* ** India's ************** ******** *** ************ *** *** ** generic **** ****** US ************* ***** ********** ****** of ************ *** ***** * ***** ***** * * ***** ********* ******* of ********* ** ********** ********** ******* in ************** ************ *** ********