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The Drugs Technical Advisory Board (DTAB), the highest statutory decision-making body on technical matters related to drugs in the country, has recommended the inclusion of all antibiotics in the definition of new drugs in the New Drugs and Clinical Trial (NDCT) Rules, 2019.

The recommendation to the Drugs Consultative Committee (DCC) is aimed at curbing the growing antimicrobial resistance which is now recognised as a public health threat globally. 

According to Rule 122 E of the Drug and Cosmetic Rules 1945, a new drug can be one which has not been used in the country and has not been recognised as effective and safe by the licensing authority for the proposed claims. It could also be an approved drug with modified or new claims including indications, dosage, and new route of administration. 

If brought into the new drug bracket, the manufacturing, marketing, and sale of antibiotics will be documented. Also, the manufacturing and marketing clearance will have to be obtained from the Central government instead of State drug administration, and patients will be able to buy antibiotics only on prescription. 

The board is also looking at amending the labelling requirements under the Drugs Rules, 1945 and adding a blue strip or box for antimicrobial products. It has recommended that no antimicrobials should be sold by the traders to the non-pharmaceutical industries who do not hold requisite licences.

A recently released report by the Indian Council of Medical Research’s Antimicrobial Resistance Surveillance Network said that drug-resistant and difficult to treat urinary tract infections, blood stream infections, pneumonia, and typhoid are among the diseases that are showing resistance to commonly used antibiotics in India.

Meanwhile, in a recent meeting, DTAB was apprised that antimicrobial resistance has been recognised as a serious and growing threat to public health globally.

“The problem of antimicrobial resistance has been highlighted as a global health priority in multiple high-level platforms and in view of this it was proposed to include all antibiotics in the definition of “new drug’’ in New Drugs and Clinical Trial Rules, 2019,” noted the minutes of the meeting.

DTAB added that antimicrobial resistance can be caused due to misuse of antibiotic, antiviral, antifungal, etc. and accordingly recommended that the matter may be deliberated in the DCC initially.



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To curb antimicrobial resistance, government may include antibiotics in definition of new drug https://artifexnews.net/article68760723-ece-2/ Wed, 16 Oct 2024 15:15:13 +0000 https://artifexnews.net/article68760723-ece-2/ Read More “To curb antimicrobial resistance, government may include antibiotics in definition of new drug” »

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The recommendation to the Drugs Consultative Committee (DCC) is aimed at curbing the growing antimicrobial resistance which is now recognised as a public health threat globally. 
| Photo Credit: Getty Images/iStockphoto

The Drugs Technical Advisory Board (DTAB), the highest statutory decision-making body on technical matters related to drugs in the country, has recommended the inclusion of all antibiotics in the definition of new drugs in the New Drugs and Clinical Trial (NDCT) Rules, 2019.

The recommendation to the Drugs Consultative Committee (DCC) is aimed at curbing the growingantimicrobial resistance which is now recognised as a public health threat globally. 

According to Rule 122 E of the Drug and Cosmetic Rules 1945, a new drug can be one which has not been used in the country and has not been recognised as effective and safe by the licensing authority for the proposed claims. It could also be an approved drug with modified or new claims including indications, dosage, and new route of administration. 

If brought into the new drug bracket, the manufacturing, marketing, and sale of antibiotics will be documented. Also, the manufacturing and marketing clearance will have to be obtained from the Central government instead of State drug administration, and patients will be able to buy antibiotics only on prescription. 

The board is also looking at amending the labelling requirements under the Drugs Rules, 1945 and adding a blue strip or box for antimicrobial products. It has recommended that no antimicrobials should be sold by the traders to the non-pharmaceutical industries who do not hold requisite licences.

A recently released report by the Indian Council of Medical Research’s Antimicrobial Resistance Surveillance Network said that drug-resistant and difficult to treat urinary tract infections, blood stream infections, pneumonia, and typhoid are among the diseases that are showing resistance to commonly used antibiotics in India.

Meanwhile, in a recent meeting, DTAB was apprised that antimicrobial resistance has been recognised as a serious and growing threat to public health globally.

“The problem of antimicrobial resistance has been highlighted as a global health priority in multiple high-level platforms and in view of this it was proposed to include all antibiotics in the definition of “new drug’’ in New Drugs and Clinical Trial Rules, 2019,” noted the minutes of the meeting.

DTAB added that antimicrobial resistance can be caused due to misuse of antibiotic, antiviral, antifungal, etc. and accordingly recommended that the matter may be deliberated in the DCC initially.



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