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Government of India. * * * * * *. Ministry of Personnel, Public Grievances & Pensions. Evaluation of RTI ACT. New Delhi: May 6, 2010. A study has been conducted through an independent organization, namely, PricewaterhouseCoopers, ..... Schedule M of Drugs and Cosmetics Rules, 1945 has been made mandatory from 1st July, 2005 for all Pharma Enterprises. The up-gradation to Schedule M by a small and medium pharma enterprise normally requires a sum of Rs. 20.00 lakh to Rs. ...

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The first permission to manufacture a new drug is given by the CDSCO on the basis of the certificate of analysis, test report, safety and efficacy data of the drug provided by the manufacturer as per the requirement of Drugs & Cosmetics Act and Rules. ... The Office of Drugs Controller General (India) (DCG) (I) had in the year 2007 prepared a list of 294 Fixed Dose Combinations (FDCs) reported to be available in the market which were not approved by DCG (I). ...

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Ephedrine is a chemical used to manufacture narcotic drugs and psychotropic substances. Banned drugs include Ecstasy and Ice contain large doses of Ephedrine. The regulated price of the substance in India is Rs. 1200 per kg, ... An ammendement in the existing drugs & cosmetics act,NDPS act to empower state drug controllers to arrest &interrogate the convicts is necessary.Also the present issue should be handed over to the DRI for a deep survey & bring out all the convicts ...

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What are fees for regulatory department in India? Balaji K. The Drugs and Cosmetics Act 122DA. – Application for permission to conduct clinical trials for New Drug/Investigational New Drug – cover the fees. ...

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... he has been active in a variety of expert groups convened by the Drugs Controller General (India) to develop GCP guidelines and review the existing Drugs and Cosmetics Act. He has been closely involved in over 200 clinical trials ...

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Karnataka pharma industry gears up for GLP compliance, organizes seminar pharmabiz.com The Drugs & Cosmetics Act has now included Schedule L1 for the implementation of the same. The state's industry which has been known to adhere to the ...

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Task force to look into pharma industry's problems: Azad Economic Times Azad assured the meeting that the ministry will issue necessary directions to states and union territories under Section 33P of the Drugs and Cosmetics Act ... and more »

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Centre to set up task force to look into issues of pharma industry, says Azad pharmabiz.com ... Section 33P of the Drugs and the Cosmetics Act so that the genuine manufactures were not harassed under various provisions of the Spurious Drugs Bill. ... and more »

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Antibiotic policy for the state soon Times of India The directorate of drugs control has been asked to look at provisions in the Drugs and Cosmetics Act to make double-prescriptions mandatory for some class ... and more »

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India`s scaling growth hits world slowdown: FIEO Chief Myiris.com ... Act, 2010 with the US authorities which will have serious implications for exports of drugs and pharmaceuticals, medical equipment, cosmetics, ...

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UP govt issues order to police to file FIR against cos marketing substandard drugs pharmabiz.com ... and the state governments under section 21 of the Drugs and Cosmetics Act, 1940 and policy guidelines issued by the Drug Controller General of India. ...

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Kerala drugs control dept takes legal action against Abbot India pharmabiz.com ... Abbot India Ltd, for violation of provisions of Drugs and Cosmetics Act and Essential Commodities Act. According to sources from the DCA, the C&F agent ...

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DCGI issues guidance on marketing approval of FDC drugs pharmabiz.com Appendix VI of Schedule Y (Drugs & Cosmetics Rules 1945) specifies the requirements for approval for marketing of various types of FDCs. ...

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Life saving now endangering Deccan Chronicle During a recent visit to the city, Mr Ashok Kumar, secretary to the government of India (Pharmaceuticals) averred, “The end product of drug manufacturing ...

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Moneylife Personal Finance Magazine

What is the extent of spurious medicines in India; 0.04% or 30% Moneylife Personal Finance Magazine Section 17 of Drugs and Cosmetics act 1940 specifies that spurious, adulterated and misbranded are counterfeits." To fight counterfeits, Mr Ray has ...

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