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In this stage we determine the efficacy and safety profiles of our generics and biosimilars vis-a-vis their original drugs.
We do comprehensive bioequivalence and
trials before arriving on
a decision to develop
the product. |
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Stability testing is a very important part of the manufacturing process.
It tells us how the formulation will
behave under various environmental conditions. As previously mentioned, we have a stringent system of internal quality control and assurance. |
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| Once the drug has been launched, our pharmacovigilance department subjects it to post marketing surveillance. |
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