The Health Ministry recently amended the Drugs and Cosmetics Rules, 1945 whereby no permission for conduct of clinical trial intended for academic purposes in respect of approved drug formulation will be required for any new indication or new route of administration or new dose or new dosage form where the trial has been approved by the Ethics Committee.
"The recent amendment will significantly reduce start-up timelines due to exemption from DCGI approval while maintaining vigilance through Ethics Committees. Thus, this will give a big fillip to these institutions, encouraging more medical practitioners to get involved in clinical research," said Shashwati Pramanik, Chair, Regulatory Council, ISCR.
In order to tackle India's unmet medical needs, there is need for greater focus on clinical research for our country, said C S Pramesh, Professor and Chief, Thoracic Surgery, Department of Surgical Oncology at Tata Memorial Hospital.
"Academic research is done to the same stringent local and international guidelines as research done by any sponsor in the country and with equal commitment to patient safety, ethics and quality.
"We have seen the tremendous benefits that cancer patients at Tata Memorial Hospital have derived from local academic research, both in terms of cost and efficacy and will continue to invest in bringing better and more cost effective treatments to patients," he added.
"A greater focus on clinical research is needed in many disease areas where there are unmet medical needs. Regulatory amendments that encourage research and innovation such as this amendment can pave the way for more breakthrough research," he added.
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