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dc.contributor.authorProf. (Dr.) Subhrangsu Shekhar Chatterji-
dc.contributor.authorJoydip Ghosal-
dc.date.accessioned2024-01-30T13:31:20Z-
dc.date.available2024-01-30T13:31:20Z-
dc.date.issued2024-01-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1381-
dc.description.abstractThe concept of outsourcing the development and global testing of new drugs has become popular in the pharmaceutical industry due to its cost and uncertainty. Due to various factors, India is considered the preferred destination for clinical trials. These include its large indigenous treatment population, human resources, technical capabilities, adoption, amendment, implementation of laws by regulators and changing economic environment. There is a high potential for multinational pharmaceutical companies being attracted to conduct their clinical trials in India due to the availability of a highly skilled workforce concentrated in a few urban areas, a large population, and the prevalence of all major diseases. Unfortunately, there have been isolated cases of supposedly unethical and improperly conducted studies. The “New Drugs and Clinical Trials Rules, 2019”, notified by the Central Drugs Standard Control Organization, will help provide Indian people with quick access to new medicine and has a slew of new provisions.en_US
dc.language.isoenen_US
dc.publisherCentre for Health Law and Policy (CHLP)en_US
dc.subjectAmendments, Clinical Trial Rules, Drug Regulatory Process, New Drug Regulationsen_US
dc.titleClinical Trials In India: Look Forward To Live Forwarden_US
dc.typeArticleen_US
Appears in Collections:CHLP Article 4

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