ASEAN harmonises drug registration norms, CTD filing to be mandatory from 2012pharmabiz.comHowever, it would also pose a threat for the country's drug research and clinical trial industry in near future, if the government of India is to neglect ...

National PostNew cholera vaccine holds promiseTheMedGuruTo test the clinical efficacy of the vaccine the researchers studied a group of 67000 people over the age of 1 year, in Kolkata, India. ...Indian cholera vaccine meets WHO normsDaily News & AnalysisAffordable cholera vaccine closer to realityReuters AlertNetClinical Trial Reveals Cholera Vaccine Is Safe, Offers Protection For Up To 2 ...Kaiser Family FoundationEmerging Health Threats Forumall 20 news articles »

Norms on human clinical trial in IndiaWebnewswire.comPrior to 17th November 2008, registration of clinical trial was voluntary. For all the clinical trials, permission of which were granted between 17th ...and more »

India needs to allow phase I trials of new drugs developed abroad ...pharmabiz.comHe added that while the west has accepted Indian Clinical Research data from phase II trials conducted in accordance with ICH GCP norms, they are keenly ...The clinical trials of mesothelioma - their purpose and benefitsMesothelioma Cancer News (press release)all 2 news articles »

No more off-the-record human clinical trialsEconomic Times, IndiaThis would make clinical trials more transparent and those conducting them more responsible and accountable,” said a health ministry official who didn't want to be named. According to existing norms, ICMR, India's apex body for biomedical research, ...Now, all human clinical trials to be registered Times of IndiaTrial registration now mandatory in India Pharma TimesThe law and clinical trials mydigitalfc.comFDA news (subscription) - pharmabiz.comall 8 news articles

Tighter norms for drug clinical trialsHindu Business Line, IndiaDetails of the clinical trials they conduct across the country are to be brought into public domain on a Web site. The CROs will have to register their trials with the Drugs Controllerate-General of India; they were advised to register with the Indian ...

DCGI initiates measures to regulate clinical trials, CROsPress Trust of India, IndiaAhmedabad, Mar 12 (PTI) Initiating a slew of measure to regulate the country's booming clinical trials market, Drug Controller General of India is conducting audits for the first time to ensure that they meet the norms besides making registration of ...DCGI to be strict with clinical trials Gujarat Global.comContract working gains heft in clinical research sector Pharma Timesall 6 news articles

Law in offing to tighten regulation of clinical trialsTimes of India, IndiaNEW DELHI: There are no laws at present to penalize and monitor pharma companies, which have messed up or violated norms while conducting global clinical trials for testing drugs in India to avoid instances like patients' deaths. ...

Health NewstrackICMR comes out strict draft norms on clinical trialsTimes of India, IndiaThe draft created jointly by ICMR, Forum for Ethical Review Committees in India and Indian Society of Clinical Research, however, points out that compensation will not be paid for failure of an investigational product to have its intended effect to ...Most trials conducted under strict FDA, European rules LivemintMany Clinical Trials Moving Overseas U.S. News & World ReportGrowth of clinical trial outsourcing raises issues CNNBizjournals.com - Calcutta Telegraphall 45 news articles

Outsourcing of Drug Trials Is FaultedNew York Times, United StatesThe report, “Ethical and Scientific Implications of the Globalization of Clinical Research,” also asks whether drug research conducted in developing countries is relevant to the treatment of American patients. “We don’t want to imagine that ...Growth of clinical trial outsourcing raises issues CNNICMR comes out strict draft norms on clinical trials Times of IndiaMany Clinical Trials Moving Overseas U.S. News & World ReportBizjournals.com - Wall Street Journalall 20 news articles