Clinical standards - Celia Ingham Clark
NHS England
Presentation from the 'NHS services open seven days a week: every day counts' event on Saturday 16 November at The Metropole Hotel, Birmingham.
This event was hosted by NHS Improving Quality and NHS England to share the views and ideas of public, patients, carers, NHS England and health and social care staff on how to improve access to services for patients across the seven day week.
More information at http://www.nhsiq.nhs.uk/improvement-programmes/acute-care/seven-day-services.aspx or #7DayServices
Clinical standards - Celia Ingham Clark
NHS England
Presentation from the 'NHS services open seven days a week: every day counts' event on Saturday 16 November at The Metropole Hotel, Birmingham.
This event was hosted by NHS Improving Quality and NHS England to share the views and ideas of public, patients, carers, NHS England and health and social care staff on how to improve access to services for patients across the seven day week.
More information at http://www.nhsiq.nhs.uk/improvement-programmes/acute-care/seven-day-services.aspx or #7DayServices
Conduct of clinical Trials during covid 19 a CTTI webinar Pamela Tenaerts
This week, stakeholders from across the clinicaltrials ecosystem submitted experiences and insights related to the FDA’s new guidance on the #conduct of clinical trials of medical products during the current hashtag#COVID-19 pandemic. We shared best practices and experiences in a webinar and our slides are now available in advance of posting the webinar.
clinical protocol & investigator information.pptx by Nitin KaleNitinKale46
What is a clinical trial protocol?
Clinical research is conducted according to a plan (a protocol) or an action plan. The protocol demonstrates the guidelines for conducting the trial. It illustrates what will be made in the study by explaining each essential part of it and how it is carried out. An Investigator is selected by the sponsor to conduct a clinical trial. An Investigator should be qualified but they don’t necessarily need to be a physician, although a medical professional should be listed as a ‘sub-investigator if that is the case.
clinical protocol & investigator information.pptx by Nitin Kale
GCPcertificate
1. NIDA Clinical Trials Network
Certificate of Completion
is hereby granted to
Swati Atale
to certify your completion of the six-hour required course on:
GOOD CLINICAL PRACTICES
MODULE: STATUS:
Introduction N/A
Institutional Review Boards Passed
Informed Consent Passed
Confidentiality & Privacy Passed
Participant Safety & Adverse Events Passed
Quality Assurance Passed
The Research Protocol Passed
Documentation & Record-Keeping Passed
Research Misconduct Passed
Roles & Responsibilities Passed
Recruitment & Retention Passed
Investigational New Drugs Passed
Course Completion Date: 2 March 2016
CTN Expiration Date: 2 March 2019
Tracee Williams, Training Coordinator
NIDA Clinical Coordinating Center
This training has been funded in whole or in part with Federal funds from the National Institute on Drug Abuse, National
Institutes of Health, Department of Health and Human Services, under Contract No. HHSN27201201000024C.