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The health ministry plans to revamp guidelines for approving biosimilar drugs to make the regulatory pathway more robust and sync it with the rapidly evolving global landscape. The guidelines were released three years ago.

Biosimilars are copies of complex drugs, which are based on living cells and 'similar' to an original biologic manufactured by the innovator. These drugs stand distinct from the chemical-based generic drugs that are 'identical' to the originator's compound.
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