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The DRKS is an open access, free of charge online register for clinical trials and is available both in English and German. DRKS is part of the WHO's ICTRP. The DRKS works with two partner registries in Germany, DeReG (German Registry for Somatic Gene-Transfer Trials) and Clinical Trial Registry of the University Medical Center Freiburg. [4]
The International Clinical Trials Registry Platform (ICTRP) is a platform for the registration of clinical trials operated by the World Health Organization. [1]The ICTRP combines data from multiple cooperating clinical trials registries to generate a global view of clinical trials worldwide, with a search portal that allows access to the entire dataset.
The CTRI requests all the information which the World Health Organization recommends for clinical trial registries. [8] Additionally, the CTRI collects information specific to the circumstances of India, including the address of the principal investigator, the name of the ethics committee overseeing the trial and confirmation of their government registration; proof of permission from the Drugs ...
Clinical trials in India refers to clinical research in India in which researchers test drugs and other treatments on research participants.NDCTR 2019 and section 3.7.1 to 3.7.3 of ICMR guidelines [1] requires that all researchers conducting a clinical trial must publicly document it in the Clinical Trials Registry - India.
The public side of EudraCT is for organisations to register any of their clinical trials as defined by Directive 2001/20/EC.The process of applying and registering a clinical trial should be completed before submitting an application to any of the Member State/s in which they anticipate running the trial.
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Clinical trial registration is the practice of documenting clinical trials before they are performed in a clinical trials registry so as to combat publication bias and selective reporting. [25] Registration of clinical trials is required in some countries and is increasingly being standardized. [ 26 ]
The clinical trial regulations (EU-CTR) ensure that the rights, safety, dignity and well-being of subjects are protected and data generated during clinical trials are robust and reliable. [2] The regulation aims to harmonize the processes for assessment and oversight of clinical trials throughout the EU.