Indian Council of Medical Research released guidelines to test medicines from AYUSH

To bring research on Ayurvedic drugs and formulations closer to practices in Western medicine, the Indian Council of Medical Research has released a set of guidelines concerning standards that must be adhered to in testing medicines from AYUSH (Ayurveda, Yoga, Unani, Siddha and Homeopathy) schools.

Key Guidelines

If a mix of medicinal systems are involved, then there ought to be experts from each of those fields supervising trials and if a product deriving from traditional knowledge were to be commercialised, the “legitimate rights/share of the tribe or community from which the knowledge was gathered should be taken care of appropriately while applying for Intellectual Property Rights and patents for the product.

The draft guidelines say that research on traditional and folk medicines and patented and proprietary varieties of traditional medicines involving human participants must be done using the same ethical principles under which drug trials are conducted.

The guidelines deal with emerging fields of research such as synthetic biology and ethical rules governing medical diagnostics, and specify that all participants be made aware of the risks and not be offered undue inducements to participate in the trial of a new drug.

Clinical trials

India has several sets of guidelines governing the conduct of clinical trials and stem cell research that are updated from time to time.

However, there has been little clarity on how Ayurvedic formulations and other traditional medicines ought to be tested.

A range of companies are employing new approaches such as genetic analysis or trying to determine the molecular basis of the effectiveness of traditional formulations.

Among others, one of India’s top pharmaceutical companies, Sun Pharma, has entered into a deal with the International Centre for Genetic Engineering and Biotechnology to develop a herbal drug for dengue earlier this year.

The ICMR guidelines are not a precursor to a law though adherence to them is required by India’s drug regulator to grant permission for trials.

India has frequently seen controversies over the improper conduct of clinical trials and there is a proposed amendment to the Drug and Cosmetics Act that seeks to impose stricter penalties for those found violating clinical trial guidelines.

Current Affairs 2nd August, 2016
Current Affairs Round Up Bullet Points, June, 2016 Current Affairs Round Up Bullet Points, May, 2016

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