NN/LM Resource Picks: AIDSource and AIDSinfo
Wednesday, November 30, 2016 1-2 pm MT/ 2-3 pm CT
Registration is required: https://nnlm.gov/ntc/classes/class_details.html?class_id=1065
More than 1.2 million people in the United States are living with HIV. Having access to quality, current information is vital in helping to improve the research, prevention, diagnosis, and treatment of HIV/AIDS. Join us to learn more about two great information resources – AIDSource and AIDSinfo. These websites feature information from both federal and nonfederal sources, and include medical practice guidelines, clinical trials, statistics, mobile apps, and so much more! Resources are useful for health professionals, researchers, educators, and the general public.
Andrew Plumer, National Library of Medicine, Specialized Information Services Division
Allison McDougal, PMP, AIDSinfo Project Manager
Discover National Library of Medicine Resources and More
October 26, 2016, 1-2 pm MT/ 2-3 pm CT
SIS Outreach Portal
Are you involved in outreach to underserved communities or special populations or know people who are and would like to learn about some wonderful free resources? Join us to learn more about key resources in the National Library of Medicine’s Outreach Activities & Resources portal. Participants will have the opportunity to try out some of the fun tools and websites for minority health, caregivers, environmental health, and more.
Registration is not required. Join the webinar at this link: https://webmeeting.nih.gov/mcr2 . The webinar will be recorded and posted to our website.
Breezing Along with the RML
October 19, 2016 at 10am MT/11am CT
The Changing World of Research
Presenter: Daureen Nesdill, Marriott Library, University of Utah
During the ‘80s the U.S. federal agencies started pushing collaborative research among universities. Since then technology has advanced and collaborations have increased so that solo researchers are hardly ever encountered. Advances in technology also led to instrumentation providing data in electronic format. Researchers found themselves in a hybrid world working with both print and electronic formats. Across the nation – actually the world – librarians have stepped-up to learn about the issues and develop programs to assist researchers in the changing world of research. This talk will present some of the initiatives developed by librarians.
To view the webinar, follow the instructions on https://nnlm.gov/mcr/education/breezing
Question! What does Noon on October 24, 2016 have in common with Pac-Man, Blinky, Inky, Pinky, and Clyde?
Ding! Ding! Ding! You guessed correctly! It is the fun packed theme being used by the RMLs at the Joint Meeting to engage attendees in sharing barriers they face and the creative ways they have overcome them. Be thinking now about all those times when you had tricky situations that needed some creative solutions to keep your library program go’n and grow’n. And for those of you who are looking for creative solutions to build up their library won’t be disappointed because there will be lots of ideas being shared. /jb
MedPrint is a joint initiative of the NN/LM and the National Library of Medicine to retain and preserve biomedical literature in print format. DOCLINE users indicate their commitment to hold a title they have in print by choosing the radio button in a journal title’s record in their serial holdings – “Will hold title for national commitment“. The NLM runs reports and if it’s a title that they still need, and if most of the issues in your title are complete, they will ask you to sign an agreement. Every MedPrint participant agrees to hold the title(s) for 25 years. It’s a long time, but it will help ensure that journal articles are accessible since access to copies in the electronic environment cannot not always be guaranteed. If you are concerned about accessibility and want to participate you can read more about the program here
Retro gaming is returning. You’ll find Pokeman Go in Des Moines, but even more important you’ll find Pac-man at the Joint Meeting! Yes, Ghost Barriers will be converging on the conference on Monday October 24, 2016 for NN/LM Pac-Man vs Ghosts: Librarians Overcome Barriers. You’ll be introduced to the RML staff of the MidContinental and Greater Midwest Regions. You’ll merge with them to battle the Ghost Barriers in the Des Moines Exhibit Hall from noon to 1:30pm. Victory will be won with strategies that overcome the challenges we face in being effective professionals. Don’t miss out on the action! /ch
The final rules (link is external) for ClinicalTrials.gov were recently released. Do you help colleagues who submit information to ClinicalTrials.gov or do you want to have a better understanding about what these rules require? The National Library of Medicine invites you to three live webinars on the final rule for Clinical Trials Registration and Results Information Submission (42 CFR part 11). The sessions will be recorded.
Link to Webinar Registration
- September 27, 2016, 11-12:30MT, 12 – 1:30pmCT – a broad overview of the final rule, including the compliance and effective dates.
- October 5, 2016, 11-12MT, 12 – 1pmCT – requirement for registering clinical trials
- October 11, 2016, 11-12MT, 12 – 1pmCT – requirements for submitting results /ch
A beta version of the Medical Subjects Heading (MeSH) Browser is ready for testing. The beta version will be available for approximately two months, until mid-November.
Both the current browser and the beta version will access the same data so that users can compare the search and retrieval functionality between the two systems. The new version is being developed to take advantage of new technology and improve functionality.
NLM would like your feedback on the beta version of the MeSH Browser during the test period. Please send comments and questions to NLM Customer Service with “MeSH Browser beta version” in the Subject field. /ch
The U.S. Department of Health and Human Services today issued a final rule (link is external) that specifies requirements for registering certain clinical trials and submitting summary results information to ClinicalTrials.gov. The new rule expands the legal requirements for submitting registration and results information. At the same time, the National Institutes of Health has issued a complementary policy (link is external) for registering and submitting summary results information to ClinicalTrials.gov for all NIH-funded trials, including those not subject to the final rule. A news release includes links that provides summaries and a table to better understand the changes.
Important elements of the final rule include:
- Providing a checklist for evaluating which clinical trials are subject to the regulations and who is responsible for submitting required information;
- Expanding the scope of trials for which summary results information must be submitted to include trials involving FDA-regulated products that have not yet been approved, licensed, or cleared by the FDA;
- Requiring additional registration and summary results information data elements to be submitted to ClinicalTrials.gov, including the race and ethnicity of trial participants, if collected, and the full protocol;
- Requiring additional types of adverse event information; and
- Providing a list of potential legal consequences for non-compliance. /ch
NLM has published an FAQ about the MEDLINE and non-MEDLINE content of the Hospital Literature Index, the Hospital and Health Administration Index, the Index to Dental Literature, and the International Nursing Index. These abstracting and indexing publications are no longer published and you may be debating whether to keep them or not. The FAQ offers some things to consider. /ch