All the manufacturers of medical devices are required to obtain a medical equipment registration and a manufacturing license as per the Drugs and Cosmetics Act. Manufacture means a process or a part of the process for creating, changing, ornamenting, accomplishing, packing, labelling and breaking up or simply adopting a drug in view of its sale as per the clause of section 3 of Drugs and Cosmetics Act.
It
has been recently notified by the Directorate General of Health Services,
Ministry of Health and Family Welfare and was recently brought to the notice of
Central Drugs Standard Control Organization or CDSCO that the medical device
manufacturers are facing some issues for establishing facilities for carrying
out certain activities like coating and sterilization.
The
manufacturers are struggling for setting up facilities to carry our functions
like assembling and coating and sterilization of devices for which CDSCO grant
licenses to all those sites for carrying out such activities. Upon asking the state
regulators to issue licenses to all those companies that wish to perform the
tasks, the realities behind the difficulties for getting the regulatory
clearances clearly come out.
This
imprint is covered by a part of the circular that states out why any regulatory
resistance to the granting of licenses runs counter to the Drugs and Cosmetics
Act. The legislation states that manufacture means any task that includes the
production, changing, packing and labelling or otherwise treating any drug or
devices. Thus, as per DGCI, coating, assembly as well as sterilization of the
medical devices are covered by the definition of manufacture.
Companies
thus need a license to perform these tasks and also by further extension, all
state agencies should give license to all organizations for meeting the requirements
for conducting these applications.
The
decision taken by CDSCO is quite obvious, since these activities are directly
associated with the medical device in some way or the other.
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