The court said the decision to include all medical devices as “drugs” was a policy matter and no case for interference was made out as there was no arbitrariness or unreasonableness.
“MHFW (Ministry of Health and Family Welfare), in its wisdom, thought it fit to bring all medical devices within the ambit of the expression ‘drug ‘. This is clearly a policy matter,” the bench, also comprising Justice Tara Vitasta Ganju, said in a recent order dated September 1.
“To our minds, there is no manifest arbitrariness or unreasonableness in the shift in policy of bringing all medical devices within the ambit of a regulatory regime. Our postscript is, if we were to allow the writ petitions, figuratively speaking, we would be throwing away the baby with the bathwater,” the court opined.
The authorities should, however, take measures to quickly iron out the kinks found while progressing the regulatory regime, the court said.
In 2018, the Centre had first brought four medical devices , i.e. nebuliser, blood pressure monitoring device, digital thermometer and glucometer, within the ambit of “drug”. In 2020, all medical devices were notified as “drugs”. The court observed that the implementation of the policy was “calibrated” and gave ample time to the manufacturers, importers, sellers and distributors, to transition to a mandatory licensing regime.
“MHFW’s reasons are manifold, which include the desire to align itself with the international regulatory regime and to further the interest of the patients. Mere errors, if any, in the policy, which is otherwise robust and devised bearing in mind patient safety, cannot be upturned by the court while exercising the power of judicial review under Article 226 of the Constitution, unless it is a clear case of demonstrable violation of fundamental rights,” the court said.