To attend, just click on 'Join Now' below: Learn about timelines for enrollment, how to use the program, how to verify new and existing employees, and exemption and exceptions for federal contractors who have been awarded a federal contract with the FAR E-Verify clause. This webinar is a chance to get some last-minute advice and settle some nerves before heading into your very own classroom for the first time. Do you or someone you know want to participate in a clinical study? Learn about creating a case, understanding case alerts, handling a TNC, employer responsibilities, and common user mistakes. PDF handouts and transcripts of each presentation are provided. Each document below is provided as a PDF file. Estimated duration: 1 hour. Confirm if everyone is well-versed with the webinar software technology and the contents of the webinar. If you have never joined a Cisco WebEx session before, please prepare your web browser before the session by following the instructions below. Webinar.net launched in 2019, designed to be a modern alternative to the dated Meeting tools that are often used for marketing and training applications, It is a powerful, easy-to-use online presentation platform with polished user interfaces. As one of the most popular webinar platforms today, you can get started with GoToWebinar with its 14-day free trial. To join a webinar, select âJoinâ 10 to 15 minutes before the scheduled start time. In addition, the ClinicalTrials.gov website and PRS have changed since these slides were developed. Summarizes who must submit "expanded" clinical trial results information, when such information must be submitted, what constitutes results information, and when the information must be updated. Official websites use .gov (October 5, 2016), Final Rule Results Information Requirements - Webinar 3 of 3 (60:03) The webinar also discussed the clinical trial information posting provisions, quality control review procedures, and when the obligation to update and correct clinical trial information ends. We discuss both of these issues. All listed times are Pacific Time. The materials listed below are from the workshops that were held in June and September 2015. Donât miss... Read More » Estimated duration: 30 minutes. Summarizes who must submit "expanded" clinical trial registration information, when such information must be submitted, what constitutes registration information, and when the information must be updated. Rebecca J. Williams, PharmD, MPH, Assistant Director, ClinicalTrials.gov, NLM If the meeting is an audio conference only, select “Information” under the Meeting tab or view meeting invitation for conference call information. The workshop will provide the attendee with basic tools for helping to ensure results from their organization are successfully submitted to ClinicalTrials.gov. A description of who must register trials and submit results information, the trials that are covered, and the deadlines by which information must be submitted, based on FDAAA and the registration policy of the International Committee of Medical Journal Editors (September 2015), NIH, Office of Extramural Research (OER) Perspective on FDAAA (PDF) The ways to access Cisco WebEx audio are: If you have any problems installing the required plug-in, please call WebEx technical support. Citizenship and Immigration Services, Immigrant and Employee Rights Section, U.S. Department of Justice, WebEx fully supports and recommends using either. Web conferencing is used as an umbrella term for various types of online conferencing and collaborative services including webinars (web seminars), webcasts, and web meetings.Sometimes it may be used also in the more narrow sense of the peer-level web meeting context, in an attempt to disambiguate it from the other types known as collaborative sessions. Webinar.net is the ⦠Share sensitive information only on official, secure websites. Updated Quality Control and Posting Procedures Webinar, Results Database Train-the-Trainer Workshop, Final Rule for Clinical Trials Registration and Results Information Submission, Overview of the Final Rule - Webinar 1 of 3, Final Rule Clinical Trial Registration Information Requirements - Webinar 2 of 3, Final Rule Results Information Requirements - Webinar 3 of 3, ClinicalTrials.gov Webinar: Updated Quality Control and Posting Procedures, Top Questions About the Updated Quality Control and Posting Procedures for ClinicalTrials.gov, Overview of FDAAA and Other Trial Registration Policies, NIH, Office of Extramural Research (OER) Perspective on FDAAA, Protocol Registration and Results System (PRS) Overview, U.S. Department of Health and Human Services. Useful for workers, worker advocates, job seekers, and employers. The workshop topics include: the basic organizational principles of the PRS results modules, step-by-step data entry instructions for common study designs, Results Review Criteria, and navigating the ClinicalTrials.gov website help resources. This joint webinar hosted by USCIS and Immigrant and Employee Rights (IER) discusses employee rights and anti-discrimination provisions during the E-Verify and Form I-9 employment eligibility verification processes. It consists of interactive presentations and hands-on results data entry exercises with the Protocol Registration and Results System (PRS). ClinicalTrials.gov staff developed the online presentations listed below to help sponsors and investigators For further assistance, you may email us:
[email protected] (normal response time is two business days), Official Website of the Department of Homeland Security, Employment Verification Webinar Flyer – Feb. 01, 2021, Employee Rights Webinar Flyer – Feb. 01, 2021, Verifying New & Existing Employees on Form I-9, Subcontractors, Independent Contractors, and Affiliates, How to Process a Tentative Nonconfirmation, Tips to Prevent a Tentative Nonconfirmation, USCIS Freedom of Information Act and Privacy Act, U.S. Useful for prospective users. Estimated duration: 1 hour. Please note that because all workshop materials were accompanied by oral presentations, the PDF files alone may not be sufficient for understanding the requirements. Secure .gov websites use HTTPS Finalize presentation slides to prevent last-minute changes. Choose the communication methods that suits best with the team. Within the United States and Canada call: 866-569-3239. Useful for prospective and new E-Verify users. The presentations below, originally offered as a series of three live webinars, provide responsible parties with information about the Final Rule for Clinical Trials Registration and Results Information Submission (42 CFR Part 11). Brian Tracy is a New York Times best-selling author who has consulted for more than 1,000 companies and addressed more than 5,000,000 people in 5,000 talks and seminars throughout the US, Canada and 80 other countries worldwide. Study record managers: refer to the Data Element Definitions if submitting registration or results information. Summarizes key provisions of the final rule, with a focus on the effective and compliance dates, applicability of the final rule, and new requirements for the submission of results information for applicable clinical trials of unapproved, unlicensed, or uncleared drug, biological, and device products. The webinar includes a line up of motivating speakers and a chance to win lots of great prizes. Available Now Price: $249.00 $249.00 Discount expires November 6, 2020 Just when we started to feel comfortable with the TCJA⦠Weâre preparing every day for the 2020/21 Federal and California Tax Update, which will be chock-full of analysis, examples, and case studies youâll need as you apply these massive changes in your practice. Why Should I Register and Submit Results? GoToWebinar: A lot of professionals use this one. An overview of the Baseline Characteristics module results requirements and step-by-step instructions for entering an example parallel design study (September 2015), Outcome Measures Module (PDF) Overview of the Final Rule - Webinar 1 of 3 (60:02) A .gov website belongs to an official government organization in the United States. The Train-the-Trainer Workshop originally planned for May 18-19, 2020, is canceled and will be rescheduled at a later date. Learn about Form I-9 requirements, step-by-step instructions on how to complete each section, acceptable documents, retention, and storage. Assign individuals activities that need to be monitored during the webinar such as polls, Q&As, group chats, etc. The workshop will also provide an overview of key laws and policies, including the registration and results submission requirements of Section 801 of the Food and Drug Administration Amendments Act of 2007 (FDAAA 801) and its implementing regulations (42 CFR Part 11). See information for patients and families. A full list of international support numbers is available on the WebEx support website. Useful for federal contractors and subcontractors affected by the E-Verify federal contractor rule. A quick overview of the E-Verify Program that includes what E-Verify is, how to enroll, and key program highlights. Join Aviation Week Network for a 30-minute ⦠The following example study records and study papers are fictional and were created to illustrate key concepts for results data entry in PRS. Final Rule Webinar Series. Useful for all employers. If you would like to provide feedback to help us further develop content and features for the PRS Guided Tutorials, please take our survey. Click the link of the session you wish to attend from the list below. Attendees are required to bring their own laptop with wireless connectivity capability. [Requires a browser that supports HTML5.] (September 27, 2016), Final Rule Clinical Trial Registration Information Requirements - Webinar 2 of 3 (59:37) Afterwards, we will send you an email confirming closed captioning has been added to your desired webinar. (October 11, 2016), ClinicalTrials.gov Webinar: Updated Quality Control and Posting Procedures (43:29) The target attendees are personnel responsible for providing ClinicalTrials.gov training and support to others at their academic institution/organization. Useful for existing users and new users. Updates will be provided when they are available.
Halloween In Massachusetts,
Luxury Sleepwear Brands,
Colemak Caps Lock,
Microwave Sausage Patties,
Living Proof Timeless Plumping Mousse Ulta,
65 Grn Using Benchmark Vs Tac,
Where Can I Buy Dunkaroo Cookie Dough,
Madina Book 2 ‑ English Key,