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Quite often generic drugs are manufactured by the same company that makes their brand-name counterparts.
The whole manufacturing process is regulated by the US Food and Drug Administration (FDA) and other relevant authorities.

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Beginning with issues particular to the pharmaceutical sector, this study analyzes the consequences of the resources out there for production, logistics prices, previous expertise and institutional setting on the sector's export growth. The next part thus presents the theoretical framework centered on resource-primarily based principle and institutional theory, together with the speculation to be examined.
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