Estimated duration: 1 hour. Study record managers: refer to the Data Element Definitions if submitting registration or results information. As one of the most popular webinar platforms today, you can get started with GoToWebinar with its 14-day free trial. 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 presentation describes the updated procedures and includes a question-and-answer session. You can access Cisco WebEx audio over the telephone or through a computer’s speakers. Don’t miss... Read More » 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) AnyMeeting: AnyMeeting is another popular webinar platform choice and offers a less expensive plan than GoToWebinar along with a 30-day free trial. 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). Useful for prospective users. It consists of interactive presentations and hands-on results data entry exercises with the Protocol Registration and Results System (PRS). Many dogs reject food in certain situations, whilst other dogs are so focused on the presence of treats, that their food-related behavior becomes problematic. Why Should I Register and Submit Results? An overview of the Outcome Measures and Statistical Analyses module results requirements and step-by-step instructions for entering an example parallel design study (September 2015), Adverse Events Module (PDF) Webinar.net is the … Include the topic, date and time of the webinar. The Train-the-Trainer Workshop originally planned for May 18-19, 2020, is canceled and will be rescheduled at a later date. Overview of FDAAA and Other Trial Registration Policies (PDF) Citizenship and Immigration Services, Immigrant and Employee Rights Section, U.S. Department of Justice, WebEx fully supports and recommends using either. 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. [Requires a browser that supports HTML5.] The workshop is best suited for individuals who have beginner or intermediate knowledge of the results database and are already familiar with the PRS, FDAAA 801, and 42 CFR Part 11. Please email your request for closed captioning to [email protected] at least five federal work days before your desired webinar. Please log in 5 minutes before the session. A summary of the overall workflow in PRS and an explanation of key tools for Administrators (September 2015), Participant Flow Module (PDF) Estimated duration: 1 hour. About Brian Tracy. No need to register! 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. Rebecca J. Williams, PharmD, MPH, Assistant Director, ClinicalTrials.gov, NLM This workshop is led by ClinicalTrials.gov staff and provides training to key personnel who are involved in submitting results to ClinicalTrials.gov for their academic organization (see "Who should attend?" The workshop is free and attendees are responsible for their own travel and hotel accommodations. The running time for each presentation is given in parentheses (minutes:seconds) after the presentation's title. If the meeting is an audio conference only, select “Information” under the Meeting tab or view meeting invitation for conference call information. Useful for federal contractors and subcontractors affected by the E-Verify federal contractor rule. Some of the behavior modification protocols discussed in this webinar involve the use of food, this in itself is a stopping point for some people. Useful for all employers. (October 11, 2016), ClinicalTrials.gov Webinar: Updated Quality Control and Posting Procedures (43:29) To join a webinar, select “Join” 10 to 15 minutes before the scheduled start time. Click the link of the session you wish to attend from the list below. A full list of international support numbers is available on the WebEx support website. An overview of the Participant Flow module results requirements and step-by-step instructions for entering an example parallel design study (September 2015), Baseline Characteristics Module (PDF) The target attendees are personnel responsible for providing ClinicalTrials.gov training and support to others at their academic institution/organization. (October 15, 2019). Consistent with 42 CFR Part 11, the National Library of Medicine (NLM) will publicly post submitted results information within 30 days of submission, regardless of whether the quality control (QC) review process is complete. Useful for workers, worker advocates, job seekers, and employers. An overview of the Adverse Events module results requirements and step-by-step instructions for entering an example parallel design study (September 2015). 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. Some webinars run a bit longer, so we recommend you choose a time when you’ll have 60 minutes […] Learn about how E-Verify works, how to enroll, program highlights, and a demonstration of the program. 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. If you have never joined a Cisco WebEx session before, please prepare your web browser before the session by following the instructions below. Overview of the Final Rule - Webinar 1 of 3 (60:02) below). In this webinar, consultant, early learning center owner and teacher of teachers, Seattle-based Miriam Dressler investigates the process by which families select the best options, and what you can do to make yourself stand out in the crowd…(without breaking the bank!) ClinicalTrials.gov staff developed the online presentations listed below to help sponsors and investigators 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. We discuss both of these issues. See information for patients and families. This is not a toll free number; it is recommended to use the phone‐in option only if you have trouble connecting to the conference using the “Call Me” or “Call Using Computer” options. 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. 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. Estimated duration: 1 hour. 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. The webinar includes a line up of motivating speakers and a chance to win lots of great prizes. 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 existing users and new users. Overview of the Final Rule - Webinar 1 of 3 (60:02) (October 5, 2016), Final Rule Results Information Requirements - Webinar 3 of 3 (60:03) The Medford School District hosted families during a webinar for on campus learning.Parents will have until the 29th to decide if they would like to send their child back to school or opt for the Medford Online Academy. Useful for prospective and new E-Verify users. Webinar: ATW Fireside Chat with Airforwarders Association Executive Director, Brandon Fried This webinar took place January 21, 2021. A lock ( A locked padlock ) or https:// means you've safely connected to the .gov website. Updates will be provided when they are available. 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. Finalize presentation slides to prevent last-minute changes. 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. Join us for a chance to hear from special guests : PDF handouts and transcripts of each presentation are provided. register studies on and submit results to ClinicalTrials.gov. Assign individuals activities that need to be monitored during the webinar such as polls, Q&As, group chats, etc. Rebecca Williams, PharmD, MPH, Acting Director, ClinicalTrials.gov, NLM, On January 1, 2020, ClinicalTrials.gov will update posting procedures for submitted results information for applicable clinical trials. In addition, the ClinicalTrials.gov website and PRS have changed since these slides were developed. Rebecca J. Williams, PharmD, MPH, Assistant Director, ClinicalTrials.gov, NLM (September 27, 2016), Final Rule Clinical Trial Registration Information Requirements - Webinar 2 of 3 (59:37) Share sensitive information only on official, secure websites. The materials listed below are from the workshops that were held in June and September 2015. Most webinars include a 30-minute presentation followed by a 15-minute question-and-answer session. Afterwards, we will send you an email confirming closed captioning has been added to your desired webinar. Secure .gov websites use HTTPS 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 workshop will provide the attendee with basic tools for helping to ensure results from their organization are successfully submitted to ClinicalTrials.gov. 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. If you would like to provide feedback to help us further develop content and features for the PRS Guided Tutorials, please take our survey. 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. Estimated duration: 30 minutes. February 15 @ 8:00 am - February 19 @ 5:00 pm; Arkansas: Soil Moisture Sensor School, Online, Feb. 16-17 February 16 @ 8:00 am - February 17 @ 5:00 pm; Corn Rootworm Control with Friendly Nematodes, Online Presentation Feb. 18 February 18 @ 8:00 am - 5:00 pm; Ogallala Aquifer Virtual Summit, Feb. 24-25 February 24 @ 8:00 am - February 25 @ 5:00 pm Please note that the Protocol Registration and Results System (PRS) may have changed since these slides were developed. Learn about Form I-9 requirements, step-by-step instructions on how to complete each section, acceptable documents, retention, and storage. Attendees are required to bring their own laptop with wireless connectivity capability. Deborah A. Zarin, MD, Director, and Rebecca J. Williams, PharmD, MPH, Assistant Director, ClinicalTrials.gov, National Library of Medicine (NLM) Official websites use .gov All listed times are Pacific Time. An overview of FDAAA compliance issues from the perspective of OER and tips and resources to help NIH extramural grantees (June 2015), Protocol Registration and Results System (PRS) Overview (PDF) Available Now Price: $249.00 $249.00 Discount expires November 6, 2020 Just when we started to feel comfortable with the TCJA… We’re preparing every day for the 2020/21 Federal and California Tax Update, which will be chock-full of analysis, examples, and case studies you’ll need as you apply these massive changes in your practice. Estimated duration: 1 hour. Join Aviation Week Network for a 30-minute … Within the United States and Canada call: 866-569-3239. If connecting through an Android device, download the free WebEx app from the Google Play Store. Space is limited. Each document below is provided as a PDF file. A quick overview of the E-Verify Program that includes what E-Verify is, how to enroll, and key program highlights. Final Rule Webinar Series. Learn about creating a case, understanding case alerts, handling a TNC, employer responsibilities, and common user mistakes. Confirm if everyone is well-versed with the webinar software technology and the contents of the webinar. PRS Guided Tutorials: Include audio narration, expandable images, downloadable PDF versions, and other interactive features. GoToWebinar: A lot of professionals use this one. Estimated duration: 1 hour. Estimated duration: 1 hour. Do you or someone you know want to participate in a clinical study? Please note that because all workshop materials were accompanied by oral presentations, the PDF files alone may not be sufficient for understanding the requirements. 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). The following example study records and study papers are fictional and were created to illustrate key concepts for results data entry in PRS. The ways to access Cisco WebEx audio are: If you have any problems installing the required plug-in, please call WebEx technical support. A .gov website belongs to an official government organization in the United States. Choose the communication methods that suits best with the team. Useful for workers, worker advocates, job seekers, and employers.

Property Transfers Ridgefield, Ct October 2020, Xtralis Vesda Panel, Pokemon Deluge Cheat, Flaps Up Takeoff, 12" Hexclad Hybrid Pan, Bts On Music Video, Msn To Dnp,