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This product is conditionally approved based on the results of protective efficacy reported in interim analysis of the international Phase Ⅲ clinical trial. The present experience with the vaccine from a Phase I/II trial up to 90 days post last - 2 - vaccination and the second interim data in approximately 30,000 healthy adults aged 18 years and older in UAE. (...) 【Adverse Reactions】 The safety of this product is evaluated through the China and international clinical trials. The China Phase Ⅰ/Ⅱ clinical trials are randomized, double-blinded and placebo parallel controlled to preliminarily evaluate the safety and immunogenicity of this product for adults 18 years and older. (...) The interim analysis results of the international Phase Ⅲ clinical trials are as following. The primary endpoint of the Phase Ⅲ clinical trial is the incidence of COVID-19 case calculated from 14 days after 2 doses, and the calculation method for vaccine efficacy based on person-year incidence is the main analysis method for vaccine efficacy.
Language:English
Score: 1086560.7 - https://www.un.org/sites/un2.u...rm_covid-19_vaccine_insert.pdf
Data Source: un
You can help by reporting any side effects you may get after vaccination to the Serum Institute of India Pvt Ltd who is the manufacturer of COVISHIELD™ vaccine on 24x7 Toll-Free Number: +91-1800 1200124 or at pharmacovigilance@seruminstitute.com. (...) The COVISHIELD™ is used in clinical trials, a number of participants received one or two doses in overseas and Indian trials. (...) In addition, you can report side effects after vaccination to Serum Institute of India Pvt Ltd who is the manufacturer of COVISHIELD™ vaccine as below. • 24x7 Call Center Toll-Free Number (For Medical and Adverse Event Related Queries Only): +91-1800 1200124 • pharmacovigilance@seruminstitute.com WHAT IF I DECIDE NOT TO GET THE COVISHIELD™ VACCINE?
Language:English
Score: 1057633.6 - https://www.un.org/sites/un2.u...eld_information_fact_sheet.pdf
Data Source: un
[22]  Trial free online access to ITU-R Recommendations and to the Basic Texts of the ITU   Français   Español     Home : Office of the Secretary General : CL : Contributions : 22 Recently posted  -  Search Meeting Documents     [22]  Trial free online access to ITU-R Recommendations and to the Basic Texts of the ITU Format Size Posted English Word   101888 bytes 2010-03-9 [22]  Arabic Word   51859 bytes 2010-03-30 [22]  Chinese Word   67293 bytes 2010-03-15 [22]  Español Word   66974 bytes 2010-03-15 [22]  Français Word   67247 bytes 2010-03-17 [22]  Russian Word   79040 bytes 2010-03-15 [22]    Document : ITU-SG CL  Contribution  22 Title : Trial free online access to ITU-R Recommendations and to the Basic Texts of the ITU Date : 2010-02-23 Source : SG Destination Groups : PL Meeting : 2010-04-13 Access : Restricted to TIES users  [ITU-SG] Top  -  Feedback  -  Contact Us  -  Copyright © ITU  2008 All Rights Reserved Contact for this page :  Webmaster Updated : 2010-05-31  
Language:English
Score: 1011909.6 - https://www.itu.int/md/S10-CL-C-0022/en
Data Source: un
[22]  Trial free online access to ITU-R Recommendations and to the Basic Texts of the ITU   Français   Español     Home : Office of the Secretary General : CL : Contributions : 22 Recently posted  -  Search Meeting Documents     [22]  Trial free online access to ITU-R Recommendations and to the Basic Texts of the ITU Format Size Posted English Word   101888 bytes 2010-03-9 [22]  Arabic Word   51859 bytes 2010-03-30 [22]  Chinese Word   67293 bytes 2010-03-15 [22]  Español Word   66974 bytes 2010-03-15 [22]  Français Word   67247 bytes 2010-03-17 [22]  Russian Word   79040 bytes 2010-03-15 [22]    Document : ITU-SG CL  Contribution  22 Title : Trial free online access to ITU-R Recommendations and to the Basic Texts of the ITU Date : 2010-02-23 Source : SG Destination Groups : PL Meeting : 2010-04-13 Access : Restricted to TIES users  [ITU-SG] Top  -  Feedback  -  Contact Us  -  Copyright © ITU  2008 All Rights Reserved Contact for this page :  Webmaster Updated : 2010-05-31  
Language:English
Score: 1011909.6 - https://www.itu.int/md/S10-CL-C-0022/_page.print
Data Source: un
The launch was aimed at building capacity of individuals and institutions undertaking clinical research in India and sharing best practices of clinical trial registration. Dr Soumya Swaminathan, Secretary, Department of Health Research & Director General, Indian Council of Medical Research (ICMR) stressed on the vision of the Clinical Trials Registry- India, which is to ensure that every clinical trial conducted in the region is prospectively registered with full disclosure of the trial data set items. (...) The Clinical Trials Registry- India (CTRI), hosted at the ICMR's National Institute of Medical Statistics, is a free and online public record system for registration of clinical trials conducted in India. (...) These modules would be deployed and made available free of cost to any researcher who registers on the CTRI,” highlighted Dr Arvind Pandey, Director, National Institute of Medical Statistics (NIMS), Clinical Trials Registry- India.
Language:English
Score: 1010533.1 - https://www.who.int/india/news...on-of-clinical-trials-in-india
Data Source: un
Furthermore poor allocation of resources for product development and financing of available interventions, and suboptimal regulatory and public health recommendations may occur where decisions are based on only a subset of all completed clinical trials. Reiteration of WHO position on clinical trial registry sites Before any clinical trial is initiated (at any Phase) its details are to be registered in a publicly available, free to access, searchable clinical trial registry complying with WHO’s international agreed standards. (...) In addition, the key outcomes are to be made publicly available within 12 months of study completion by posting to the results section of the primary clinical trial registry. Where a registry is used without a results database available, the results should be posted on a free-to-access, publicly available, searchable institutional website of the Regulatory Sponsor, Funder or Principal Investigator. (...) Reporting of past clinical trials results Unreported clinical trials conducted in the past are to be disclosed in a publicly available, free to access, searchable clinical trial registry.
Language:English
Score: 1003021.5 - https://www.who.int/news/item/...pan-primary-registries-network
Data Source: un
Receive free email alerts when new articles cite this article. (...) Over half (57%) the businesses were totally smoke-free. A quarter provided one or more separate smoke-free rooms, 13% had smoke- free areas within larger rooms, and 5% had a combination of smoke-free rooms and areas. Pubs and bars generally provided smoke-free rooms (59%), or smoke-free areas (32%), often in eating or “family” areas.
Language:English
Score: 985573.6 - https://www.who.int/fctc/treat...s/ArtElevenWillemsenTwenty.pdf
Data Source: un
INTRODUCTION 2 1.1 APIRG 21 item 3.2.3 discussed issues on improved Operations through Enhanced En- Route Trajectories under ASBU modules noted with appreciation that some AFI FIRs in the region were ready to begin free routing trials, and that they should build on the experience gained in other such initiatives e.g. (...) It was agreed then that AAO/SG would facilitate implementation actions by States and ANSPs that were ready to commence free routing trials and coordinate such trials between the applicable FIRs. (...) Ensure FRA implementation lessons learnt from individual states implementation are shared among participating ANSPs/States in order to improve effectiveness of the processes, with focus of safety of flight operations. --------------- 1. introduction 1.1 APIRG 21 item 3.2.3 discussed issues on improved Operations through Enhanced En-Route Trajectories under ASBU modules noted with appreciation that some AFI FIRs in the region were ready to begin free routing trials, and that they should build on t... 1.2 Free Route operations enable airspace users to fly as closely as possible to their preferred trajectory without being constrained by fixed airspace structures or fixed route networks.
Language:English
Score: 967339.1 - https://www.icao.int/WACAF/Doc...AO%20SG-3_WP3A4_CONOPS_Eng.pdf
Data Source: un
-40G/WDM, 160G, field trial, Raman amplification, etc.,: Mr. F. Kueppers, Deutsche Telekom, Germany Français   Español Print Version Office of the Secretary General Radio- communication (ITU-R) Telecom Standardization (ITU-T) Telecom Development (ITU-D) TELECOM Exhibitions and Forum Membership Home Page : Publications [S6PM-P01rev] What's coming next? -40G/WDM, 160G, field trial, Raman amplification, etc.,: Mr. F. Kueppers, Deutsche Telekom, Germany   Availability : Free Download View or Download Document Format Size Posted Free Download English   PDF (acrobat) 1.4 mb Jul 19 2002   ZIPPED PDF 1.3 mb Jul 19 2002 Top  -  Feedback  -  Privacy  -  Copyright © ITU 2001  All Rights Reserved Contact for this page :  webmaster@itu.int Updated : 2007-03-30  
Language:English
Score: 964733.8 - https://www.itu.int/itudoc/itu...workshop/optical/s06-p01r.html
Data Source: un
Following a written request by Ntuyahaga to be set free in Tanzanian territory, specifically in Dar es Salaam, he was released by the Tribunal in the Tanzanian capital. It will be recalled that, shortly after the Trial Chamber's decision of 18 March, Ntuyahaga sent a written request to the Registry, seeking permission to remain temporarily in the Tribunal's detention facilities of his own free will pending the completion of arrangements to implement the court's decision. (...) Georges Amegadjie, on 22 March and addressed to the Trial Chamber, requesting a stay of execution of the Chamber's decision ordering his immediate and unconditional release from the Tribunal's custody while he pursued an appeal against the Chamber's decision not to acquit him.
Language:English
Score: 962441.8 - https://unictr.irmct.org/en/node/1859
Data Source: un