#IRB software

[theconcinnitycompany]

7 Ways Data Monitoring Committees Can Improve Clinical Trial Trust

Sponsors of clinical trials are under pressure to maintain patient safety and data quality, but the process is time-consuming and challenging to manage. This is where more intelligent clinical trial oversight software comes in handy. The correct clinical trial oversight software can automate many of the tasks associated with clinical trial oversight, improving sponsor trust.

[sudheervanguri]

Fresher Research Consultant Vacancies in Bangalore | Advarra Job Opportunities Are you a fresh graduate looking to start your career in clinical research? Advarra, a leading player in the clinical research industry, is offering exciting opportunities for fresher Research Consultants in Bangalore. This role is perfect for candidates with a degree in clinical research or related fields who are passionate about advancing human health. Read on to learn more about the vacancy, qualifications, and how to apply. About Advarra Advarra is a global leader in clinical research and ethical review services, dedicated to improving human health through innovation and collaboration. With a strong focus on aligning patients, sites, sponsors, and CROs in a connected ecosystem, Advarra accelerates clinical trials and brings impactful therapies to the market faster. Job Overview: Research Consultant Role As a Fresher Research Consultant at Advarra, you will play a crucial role in supporting the Institutional Review Board (IRB) services. This position involves working with Advarra’s Clinical Trial Management Software (CTMS) and the CIRBI system to enhance research effectiveness and streamline study startup timelines. You will be responsible for various tasks, including translation management, safety reporting, ongoing reviews, and IRB submissions. Key Responsibilities CTMS and IRB Support: Develop familiarity with Advarra’s Clinical Trial Management Software and CIRBI system to assist in study startup activities. Customer Escalation Management: Monitor and resolve customer escalations promptly to ensure a smooth study startup process. Documentation and Reporting: Utilize internal case management and reporting software to track and complete daily/weekly work assignments. Team Collaboration: Actively participate in team meetings and contribute to discussions on customer cases and protocols. [caption id="attachment_100896" align="aligncenter" width="640"] Fresher Research Consultant Vacancies in Bangalore | Advarra Job Opportunities[/caption] Qualifications Required Basic Qualifications: Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice (GCP) guidelines. Strong organizational and administrative abilities. Familiarity with MS Office and business software. Preferred Qualifications: 0-1 year of internship experience in clinical trial coordination, study startup, regulatory affairs, or clinical data management. Excellent communication skills and a proactive attitude. Ability to work independently and as part of a team. Location and Work Environment This position is based in Bangalore, India. The role requires on-site presence, where you will work in a dynamic and collaborative environment. Advarra values its employees and fosters an inclusive culture that encourages growth, teamwork, and innovation. Apply Now to Join Advarra If you are a fresh graduate eager to contribute to the world of clinical research, don’t miss this opportunity to join Advarra as a Research Consultant in Bangalore.  Apply now

[protectionvisa]

Requirements for a protection visa in Canada

Requirements for a protection visa in Canada Canada, acknowledged for its diverse existence and hospitable humans, is a properly-appreciated tour vacation spot for those in search of protection from persecution. If you're considering applying for a protection visa in Canada, you should be aware of the specific requirements and alertness procedures concerned. This manual will offer a thorough analysis of the important steps and conditions for acquiring a protection visa in Canada. Click here for more info.

Understanding the Protection Visa A safety visa, frequently called a refugee visa, lets individuals who fear persecution in their domestic country seek asylum in Canada. This visa is designed to defend the ones prone to severe harm, ensuring they are able to stay competently and securely. Who qualifies for a safety visa? To be eligible for a protection visa in Canada, you need to satisfy the precise criteria stated inside the beneficial resource section of the Immigration and Refugee Protection Act (IRPA). The important requirements consist of:

1.Well-based Fear of Persecution: •You need to show a properly-based total fear of persecution primarily based on race, religion, nationality, club in a particular social institution, or political opinion. •The persecution desires to be immoderate and systemic, threatening your lifestyle, freedom, or fundamental human rights.

2.Unable to Seek Protection Within the Home Country: You ought to show that you are unable or unwilling to try to find protection from your home country. Due to the concern of persecution.

Admissibility: You ought to now not be inadmissible to Canada on grounds such as safety issues, criminal sports activities, human rights violations, or health motives. The Application Process: Applying for a protection visa in Canada involves several steps:

4.Claiming Asylum: You should make an asylum assertion both at a port of entry (e.g., an airport or land border) or in internal Canada at an Immigration, Refugees, and Citizenship Canada (IRCC) place of business.

5.Submitting Your Application: Complete the favored office work and discover it in the aspect of assisting files that offer proof of your fear of persecution. This can embody private statements, affidavits, statistics articles, and critiques from human rights organizations.

6.Interview for Eligibility: An immigration officer will interview you to determine if your announcement qualifies for referral to the Immigration and Refugee Board (IRB).

7.IRB Hearing: Your statement will be cited to the IRB for listening if it is determined to be eligible. During this listening, you can gift your case and offer proof to support your claim.

8.Decision: The IRB will make a choice based totally on the proof supplied. If your announcement is time-commemorated, you will be granted a refugee reputation and might get an everlasting house in Canada. Supporting Documents: To beef up your utility, it's very important to offer complete help files, including:

Identification Documents: Passports, delivery certificates, and some other applicable identification papers. Evidence of Persecution: Police reviews, clinical facts, snap shots, and witness statements. Country Conditions: Reports and articles that illustrate the situation in your own home country and the dangers you face.

Legal Assistance: Navigating the asylum technique may be complex, and it's really useful if you're looking for criminal assistance. Immigration lawyers or authorized representatives permit you to understand the requirements, prepare your software, and represent you during the hearing. Conclusion: Applying for a protection visa in Canada is a multi-step process that calls for thorough training and clear information on the eligibility criteria. By collecting compelling evidence and seeking felony steerage, you may enhance your probability of a hit application and secure a safe future in Canada.

Canada remains dedicated to offering shelter to those in need, and information on the protection visa requirements is step one in the direction of finding safety and stability in a new country.

[optionperks]

Top Gainers and Losers today on 7 June, 2024: Mahindra & Mahindra, Wipro, SBI Life Insurance Company, Tata Consumer among most active stocks; Check full list here

Top Gainers and Losers Today : The Nifty index closed at 22821.4, up by 2.05%. Throughout the day, the Nifty reached a high of 23320.2 and a low of 22789.05. The Sensex traded between 76795.31 and 74941.88 and closed 2.16% higher at 75074.51, which was 1618.85 points above the opening price. The Nifty Midcap 50 underperformed the Nifty 50, closing 1.55% higher. On the other hand, small cap stocks outperformed the Nifty 50, with the Nifty Small Cap 100 ending at 16826.1, up by 389.45 points and 2.31% higher.

The Nifty 50 has provided the following returns:

In the last 1 week: 3.36%

In the last 1 month: 4.42%

In the last 3 months: 3.53% Nifty Index Top Gainers and Losers Today The top gainers in the Nifty index were Mahindra & Mahindra (up 5.84%), Wipro (up 5.11%), Tech Mahindra (up 4.57%), Infosys (up 4.17%), and Ultratech Cement (up 4.06%). The top losers in the Nifty index were SBI Life Insurance Company (down 1.18%) and Tata Consumer (down 0.37%). The Bank Nifty ended at 49291.9, with an intraday high of 49943.2 and a low of 49080.45. The Bank Nifty's performance in the following time frames is as follows:

In the last 1 week: 1.62%

In the last 1 month: 3.09%

In the last 3 months: 4.06%

In the last 6 months: 6.27%

In the last 1 year: 12.43%

Here is the list of top gainers and losers in different indexes during the trading session on 07 Jun, 2024:

Sensex Top Gainers And Losers Today

Top Gainers: Mahindra & Mahindra (up 5.83%), Wipro (up 5.09%), Tech Mahindra (up 4.50%), Infosys (up 4.13%), and Tata Steel (up 4.04%)

Top Losers: N/A

Nifty Top Gainers And Losers Today

Top Gainers: Mahindra & Mahindra (up 5.84%), Wipro (up 5.11%), Tech Mahindra (up 4.57%), Infosys (up 4.17%), and Ultratech Cement (up 4.06%)

Top Losers: SBI Life Insurance Company (down 1.18%) and Tata Consumer (down 0.37%)

Nifty MidCap 50 Top Gainers And Losers Today

Top Gainers: L&T FINANCE, Vodafone Idea, Persistent Systems, Coforge, and Steel Authority Of India

Top Losers: Page Industries, Oberoi Realty, Jubilant Foodworks, Escorts Kubota, and Petronet LNG

Nifty Small Cap 100 Top Gainers And Losers Today

Top Gainers: Amara Raja Energy & Mobility, IRB Infrastructure Developers, Great Eastern Shipping Company, Sonata Software, and Raymond

Top Losers: JBM Auto, Finolex Cables, Glenmark Pharmaceuticals, Triveni Turbines, and Nippon Life

[ligiaonwlz]

To all of my SCI family, colleagues, and friends!

Please participate in a study to help individuals with spinal cord injury

improve their physical activity levels in the community!

If you are interested, here are the details..

If you are an individual with spinal cord injury, you may be eligible to participate if you...

are between 18 and 75 years of age

are at least 6 months post-injury and medically stable

use a manual or power wheelchair in the community

use you upper arms for exercise

are able to use a smartphone and a smartwatch independently

are interested in starting an exercise program

do not have health conditions that medically restrict you from physical activity

Time Commitment:

You will be enrolled in the study for 24 weeks (~6 months)

Number of visits:

A member of the research team will meet with you four times at your home or via a video conference meeting software.

Testing:

You will be using a smartphone based physical activity monitor system that will measure your physical activity in the community. You will also be required to answer questions related to your physical activity on a regular basis.

Compensation:

Participants can receive up to $20 per month for six months of the study and $40 for interviews and equipment return.

This information was approved by Temple University for public display and is associated with IRB Approved Protocol 27338

If Interested, Click Here!

or contact:

Shivayogi Hiremath, PhD

Shiv.Hiremath@temple.edu

215-204-0496

Twitter

Facebook

Website

Copyright © 2024, North American Spinal Cord Injury Consortium, All rights reserved.

[sindhu1901]

Speech Project Research by EverythingALS

Advancing the Diagnosis and Prognosis of ALS from Speech

They are looking for Individuals Diagnosed or Probable with Amyotrophic Lateral Sclerosis (ALS) and Healthy Participants to help give 5 speech recordings with total 75 minutes over 5 months

Their IRB approved study is motivated by the need for early detection and improved prognostic accuracy of ALS using advanced computational technology and speech data (audio, video). By participating in this study, you will contribute to a growing large ALS dataset and further advance current knowledge relating to the decline in speech due to ALS while also improving the performance of this technology.

The approach will be to perform analysis of ​online audio/video recordings: ​The study activity involves the use of Modality.ai Inc.’s web-based software that collects speech audio and video data and then uses AI and machine learning algorithms to analyze facial and speech metrics. Data collection can be conducted anywhere you feel comfortable (e.g., your home). One session per month over 5 months, and each session will last approximately fifteen minutes.

Continue reading — https://www.everythingals.org/speechproject

[chandupalle]

3D Printing Robot Industry worth USD 3.2 billion by 2028

The report "3D Printing Robot Market by Component (Robot Arms, 3D Printing Heads, Software), Robot Type (Articulated Robots, Cartesian Robots, SCARA Robots, Polar Robots, Delta Robots), Application, End-user Industry and Region - Global Forecast to 2028" The 3D printing robot market is projected to grow from USD 1.6 billion in 2023 and is estimated to reach USD 3.2 billion by 2028; it is expected to grow at a Compound Annual Growth Rate (CAGR) of 14.6% from 2023 to 2028. The growth of the 3D printing robot market is driven by reliance on automated solutions to conduct repetitive tasks and improve workplace safety, and rising awareness about higher degree of freedom offered by 3D printing robots than traditional printers.

By component, the 3D printing Head segment is projected to grow at high CAGR of the 3D printing robot market during the forecast period.

The 3D printing head segment is positioned for robust growth over the forecast period. 3D printing heads, or extruders, present a host of valuable advantages in the realm of additive manufacturing. These heads boast versatility, capable of accommodating a broad spectrum of materials, from PLA (polylactic acid), PETG (polyethylene terephthalate glycol), TPU (thermoplastic polyurethane), and ABS (acrylonitrile butadiene styrene) to metals, enabling their application across diverse industries. Renowned for their precision, 3D printing heads can meticulously create objects in the X, Y, and Z axes, resulting in highly accurate prints with exceptional surface quality. Additionally, their ability to operate at high speeds contributes to shorter production times. Furthermore, these heads exhibit efficiency by judiciously utilizing filament material through controlled deposition. Their user-friendly nature, often arriving pre-calibrated, appeals to both novices and experts. This facilitates widespread adoption across industries, such as aerospace, automotive, and consumer goods, where their advantages are increasingly appreciated.

Functional Part Manufacturing segment is projected to grow at high CAGR of 3D printing robot market during the forecast period.

The functional part manufacturing segment is expected to grow at high CAGR in the 3D printing robot market during the forecast period. 3D printing, particularly in conjunction with robots, is revolutionizing functional part manufacturing across several key industries. In aerospace, automotive, and electronics, the demand for lightweight, durable, and precision-engineered components is met through 3D printing with robots. These robots enable the creation of intricate parts with complex geometries, surpassing the limitations of traditional manufacturing methods. The versatility of 3D printing robots, accommodating various materials, including plastics, metals, and ceramics, proves invaluable. As these robots continue to advance, they are poised to enhance functional part manufacturing in these industries, as well as in consumer goods, energy, construction, and more, promising a future of innovation and efficiency.

Download PDF Brochure @ https://www.marketsandmarkets.com/pdfdownloadNew.asp?id=13451083

Noth America is poised for significant growth in the 3D printing robot market by 2028.

The North American 3D printing market is poised for significant growth in the upcoming years due to various essential drivers. 3D printing robots offer solutions to key challenges in the North American construction sector. They reduce the demand for highly skilled workers, enhance safety by handling hazardous tasks, cut costs, boost productivity, and elevate project quality. While facing developmental hurdles, such as speed and material limitations, these robots hold substantial promise for revolutionizing the construction industry and making it more efficient and sustainable. For instance, in May 2022, Cornell University’s Bovay Lab (New York) integrated ABB’s 6,000-pound IRB 6650S Industrial Robot from Switzerland for large-scale 3D printing in construction. This innovation advances robotic construction research, providing students with practical experience and enhancing sustainability and efficiency in the field. The robot, with a 12-foot track, offers a 12-foot circular reach, covering an 8x30-foot area. It is a significant step in utilizing 3D printing robots for construction and enhancing the construction sector in North America.

Key Players

Key companies operating in the 3D printing robot market are KUKA AG (Germany), ABB (Switzerland), Yaskawa Electric Corporation (Japan), FANUC CORPORATION (Japan), Universal Robots A/S (Denmark), Massive Dimension (US), CRAD B.V. (Netherlands), Caracol (Italy), among others.

About MarketsandMarkets™

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The B2B economy is witnessing the emergence of $25 trillion of new revenue streams that are substituting existing revenue streams in this decade alone. We work with clients on growth programs, helping them monetize this $25 trillion opportunity through our service lines - TAM Expansion, Go-to-Market (GTM) Strategy to Execution, Market Share Gain, Account Enablement, and Thought Leadership Marketing.

Built on the 'GIVE Growth' principle, we work with several Forbes Global 2000 B2B companies - helping them stay relevant in a disruptive ecosystem.Our insights and strategies are molded by our industry experts, cutting-edge AI-powered Market Intelligence Cloud, and years of research.The KnowledgeStore™ (our Market Intelligence Cloud) integrates our research, facilitates an analysis of interconnections through a set of applications, helping clients look at the entire ecosystem and understand the revenue shifts happening in their industry. To find out more, visit www.MarketsandMarkets™.com or follow us on Twitter, LinkedIn and Facebook.

[evoldir]

Fwd: Workshop: CzechRepl.Phylogenomics.Jan21-Feb3

Begin forwarded message: > From: evoldir@evol.biology.mcmaster.ca > Subject: Workshop: CzechRepl.Phylogenomics.Jan21-Feb3 > Date: 18 October 2023 at 06:03:29 BST > To: rdmpage@gmail.com > > > > +++ Deadline for application is Oct 18, 23:59 CEST +++ > > Dear Colleagues, > > We’re excited to announce that the Workshop on Phylogenomics will > return to Cesky Krumlov from 21-January through 3-February 2024! > > The Workshop will bring together an international collection of faculty > members and workshop participants to study and discuss current ideas > and techniques for exploring phylogenomics.  The Workshop will consist > of a series of lectures, demonstrations and computer laboratories that > cover theoretical and conceptual aspects of large-scale phylogenetics > and phylogenomics, with a strong emphasis on data analysis. > > Topics of the Workshop are diverse and include: > > Introduction to Phylogenomics: data matrix assembly (e.g., > alignment, trimming, partitioning, concatenation) and tree > visualization.State-of-the-art methods and software used in > phylogenomic inference (Concatenation and coalescent methods, > machine learning, etc.)Orthology, paralogy, and evolution of > gene familiesTrait evolution on treesPhenotypic and species > diversificationMacroevolutionary genotype-phenotype association > studiesIncongruenceGreen computingPhylogenomics in deep timeHorizontal > gene transferTarget capture sequencing approaches in phylogenomics > > The line-up of speakers/faculty includes > - Olivier Gascuel (Institut de Systématique, Évolution, Biodiversité, >  MNHN, Paris, France), > - Hélène Morlon ( Institute of Biology at the Ecole Normale >  Supérieure, Paris, France), > - Alexey Kozlov (Heidelberg Institute for Theoretical Studies, Germany), > - Lisa Pokorny (Royal Botanic Garden, Madrid, Spain), > - Jordi Paps (University of Bristol, UK), > - Marina Marcet-Houben (Barcelona Supercomputing Center, Spain), > - Laura Eme (Université Paris-Saclay, France), and Kerstin Lindblad-Toh >  (Uppsala University and Broad Institute), among others. > > The Workshop is organized by Anna Karnkowska (University of Warsaw), > Antonis Rokas (Vanderbilt University), Toni Gabaldon (IRB Barcelona, > Barcelona Supercomputing Centre) and Rosa Fernandez (Institute of > Evolutionary Biology CSIC-UPF, Barcelona) and supported by an excellent > team of Teaching Assistants. > > The Workshop on Phylogenomics will take place in the idyllic village (and > UNESCO world heritage site) of Cesky Krumlov, located in the Southern > Bohemian region of the Czech Republic from January 21 to February 3, > 2024. Applications for the workshop via the website will open shortly > and be open until Oct 18. Applications received after the deadline will > be placed on the waiting list. > > Please check the website > https://ift.tt/BEdecwh for > updated information on the schedule, faculty and for submitting your > application. We look forward to seeing you there! > > Is the Workshop on Phylogenomics too specific or not the right > match for your needs? Check out the awesome Workshop on Genomics > (https://ift.tt/7BdzYhl) for a zero-to-hero course > getting you into bioinformatics! > > "Steffen, Karin"

[sayali01]

The Basics of Clinical Trials: What You Need to Know

Clinical trials are the lifeblood of medical progress, driving innovation and shaping the future of healthcare. They are meticulously designed research studies that assess the safety and efficacy of new medical treatments, therapies, or interventions. In this article, we will delve into the fundamental aspects of clinical trials, offering insights from clinical research blogs, software development updates, and clinical research latest updates. Whether you're a prospective participant, a curious individual, or a healthcare enthusiast, understanding the basics of clinical trials is essential.

1. Why Clinical Trials Matter

Clinical trials are the bridge between scientific discovery and patient care. They play a pivotal role in:

Advancing Medicine: Clinical trials lead to the development of new drugs, treatments, and therapies.

Evidence-Based Care: They provide the evidence needed to determine whether a new approach to treatment is safe and effective.

Patient-Centered Care: Clinical trials focus on improving patient outcomes and enhancing the quality of healthcare.

2. The Phases of Clinical Trials

Clinical trials progress through several phases, each serving a specific purpose:

Phase I: These trials involve a small number of healthy volunteers and aim to assess safety, dosage, and side effects.

Phase II: In this phase, the focus shifts to a larger group of patients to evaluate the treatment's effectiveness and further assess safety.

Phase III: These trials involve an even larger patient population and compare the new treatment to existing standard treatments.

Phase IV: After approval, Phase IV trials monitor the treatment's long-term safety and effectiveness in real-world settings.

3. Informed Consent

Informed consent is a cornerstone of ethical clinical research. Before participating in a clinical trial, individuals must be provided with comprehensive information about the study, including its purpose, risks, benefits, and alternatives. Consent is entirely voluntary, and participants have the right to withdraw at any time without consequences.

4. The Role of Placebos

In some clinical trials, placebos are used to maintain scientific rigor. A placebo is a substance with no therapeutic effect. They are essential for ensuring that the treatment's benefits are not influenced by psychological factors and that any observed improvements are genuinely due to the treatment being tested.

5. The Importance of Control Groups

Control groups are a critical component of clinical trials. These groups receive either the current standard treatment or a placebo, allowing researchers to compare the new treatment's effectiveness. Control groups are essential for establishing the treatment's true impact.

6. Randomization and Blinding

Randomization involves randomly assigning participants to either the treatment or control group, reducing the risk of bias. Blinding, on the other hand, can be single-blind (participants are unaware) or double-blind (both participants and researchers are unaware of group assignments). These practices ensure the objectivity of trial results.

7. Ethical Oversight

Clinical trials are subject to rigorous ethical oversight. Institutional Review Boards (IRBs) or Ethics Committees review and approve trial protocols to ensure that the study is conducted safely and ethically. Protecting participants' rights and safety is of paramount importance.

8. The Inclusion and Exclusion Criteria

Clinical trials have specific inclusion and exclusion criteria to ensure that the participants are the right fit for the study. Inclusion criteria define who can participate, while exclusion criteria identify those who cannot. These criteria are crucial for patient safety and the validity of the trial results.

9. Monitoring and Data Collection

Clinical trials are closely monitored to ensure patient safety and data accuracy. Researchers collect data on the treatment's efficacy, side effects, and any adverse events. This data is meticulously analyzed to draw meaningful conclusions about the treatment's impact.

10. The Potential Risks and Benefits

Participating in a clinical trial comes with potential risks and benefits. Risks may include side effects, inconveniences, or the possibility that the treatment is ineffective. Benefits may include access to cutting-edge treatments, close medical monitoring, and the satisfaction of contributing to medical science.

11. Conclusion: The Road to Medical Advancement

Clinical trials are the foundation upon which medical progress is built. They are the culmination of years of scientific research and have the potential to improve patient care and save lives. By understanding the basics of clinical trials, you not only become an informed patient but also appreciate the dedication of researchers, the vigilance of ethical oversight, and the promise of a healthier future. Clinical research blogs, software development updates, clinical research companies in Pune, and medical professionals are all working tirelessly to ensure that clinical trials continue to drive innovation and bring hope to patients around the world.

[mollybrown423-blog]

What is the deal with influencers?

This week’s readings discuss influencers on social media, ethically researching sensitive populations online and the growth of TikTok. I remember that early in the course, we discussed ethics in getting social media data. It is kind of hard to believe how easy it is to get information once you know how to use the software. Proferes et al. (2021) demonstrated the problems with using Reddit as a data source. I was surprised that only 101 of the studies they looked at had mentioned IRB. I think it was so surprising because we are held to such high standards and have to go through a lengthy process to be able to conduct research, and we are only students. Professionals should be held to the same standards. I like the authors’ recommendation that researchers should contemplate risks to users if they include quotes or usernames. People might feel like they can speak more freely on platforms like Reddit and be unaware that their data could be used in a future study. I don’t have a Reddit, so I don’t know firsthand how much people share, but regardless, researchers should have to go through the IRB process to minimize harm among participants.

Bhandari and Bimo (2022) examine why TikTok is so popular and offer the framework of the “algorithmized self.” I think that their results might have been more robust if they had included a survey in addition to their interviews. Regardless, the authors presented interesting findings. Their main takeaway is the “algorithmized self,” which is a “conceptualization of the changing nature of self-making online,” (pg. 5). Instead of the “self” coming from social ties, it comes from reflexive engagement, so forming ourselves out of our acts. I think this speaks to how well TikTok caters to our personalities and has changed the social media experience. I do believe that TikTok and the “algorithmized self” are valid to some extent, but we are also shaped by our social ties. 

Brooks et al. (2021) discuss how influencers come to have celebrity status. An influencer that immediately came to my mind while I read this is Alix Earle. She has acquired celebrity status and is one of the biggest platforms on TikTok. Seeing this process broken down was great because I know a few aspiring influencers who post all the time, which I now know is called attention labor, and it makes sense why you need to work hard to get attention and build communities. Thinking about influencers in comparison to traditional celebrities, I trust influencers more to an extent. When I see a celebrity advertising a product, I am immediately skeptical because I know they are probably getting paid to say things. When I see an influencer promoting a product, I am more open to exploring that product. The authors mention that influencers work with brands, which I think is what makes it seem more authentic. They aren’t forced to say anything and can be more truthful because that company isn’t their job. 

Overall, these readings were informative about important topics. I gained a deeper understanding of ethically researching online, social media influencers and TikTok. 

[wpaannouncements]

Apply: 2023 IWCA Dissertation Grant

The deadline for the submission of an application for the 2023 IWCA Dissertation Grant is a month away. The International Writing Centers Association (IWCA) serves to strengthen the writing center community through all of its activities. The organization offers The IWCA Dissertation Research Grant to support doctoral students as they work on writing center-related dissertations. The grant is intended to fund expenses incurred by doctoral students who are working toward completion of a dissertation and a doctoral degree. The funds may be used for living expenses; supplies, materials, and software; travel to research sites, to present research, or to attend conferences or institutes relevant to the profession; and other purposes not covered here but supportive of a dissertating graduate student. Doctoral students who have an approved prospectus and are at any stage of research/writing beyond the prospectus are encouraged to apply. Grant recipients will receive a $5000 check from IWCA upon selection as the award winner. Complete application packets will contain the following items in one pdf file. Cover letter addressed to current chair, (Lawrence Cleary, lawrence.cleary@ul.ie) IWCA Grants Committee. The cover letter sells the IWCA Board on the mutual benefits that will result from their financial support. Anything that applicants do to link this project to their specific career goals and to the needs of the writing center community is welcome. It should include the following: Request IWCA’s consideration of the application Introduce the applicant and the project Outline plans for completion of the project Curriculum Vitae Approved prospectus Two letters of reference: One from the dissertation director and one from a second member of the dissertation committee For full consideration, your project MUST have all required approvals, including but not limited to institutional IRB approval.  Grant recipients will agree to the following: Acknowledge IWCA support in any presentation or publication of the resulting research findings Forward to IWCA, in care of the Grants Committee Chair, copies of resulting publications or presentations File a progress report with the IWCA, in care of the Grants Committee Chair, due within twelve months of receipt of grant monies. Upon completion of the project, submit a final project report and a PDF of the completed dissertation to the IWCA Board, in care of the Grants Committee Chair Strongly consider submitting a manuscript based on the supported research to one of the IWCA affiliated publications: The Writing Center Journal or The Peer Review. Be willing to work with the editor(s) and reviewer(s) to revise the manuscript for possible publication NOTE: The cover letter sells the IWCA Board on the mutual benefits that will result from their financial support. Anything that applicants do to link this project to their specific career goals and to the needs of the writing center community is welcome. Open from February 1, 2023 to April 15, 2023 Consider submitting your application.   Kind regards, Lawrence   Lawrence Cleary Director Regional Writing Centre C1065 Main Building University of Limerick, Limerick, Ireland lawrence.cleary@ul.ie writingcentre@ul.ie   via Email March 13, 2023 at 07:52PM

[theconcinnitycompany]

5 Ways To Streamline Virtual Trial Management With The Right Tech Stack

As the world becomes increasingly reliant on technology, it is no surprise that the clinical trial field is following suit. Virtual trials, also known as remote or decentralized clinical trials, involve using technology to collect data and monitor patient health remotely instead of in a traditional brick-and-mortar clinic setting. Successful virtual trials are built on a technology stack that meets the critical needs of virtual trials. This blog post outlines five essential technical requirements that your tech stack must support to drive successful virtual trial completion. 

[gnavalta-acmwo-capstone]

Planning (Pre-Production) through Weeks 4 and 5

Bi-Weekly Reflection - Tumblr Update #2.1

Where am I now? -- I am just about wrapping up all of the Pre-Production necessities and very close to being ready to start the Execution phase of my project! I've created photo installation mockups as well as starting to workshop the nature of each individual profile down to the following elements: 1) processing/treatment selection (b/w), 2) paper type and color (# type and regular/matte for paper), 3) frame type (Cricut paper vs. print), 4) frame size (.25", .5", .75", vs 1"), and 5) where personality type will live (front vs back). Followed up with Dr. Aumer (Institutional Review Board update) to see if I will need IRB approval to move forward; my project does not seem to be subject/human research, so I will continue as planned. Signing documents, disclaimers, and Google Forms have been drafted and ready to go to streamline the in-person project asset collection.

Where am I headed? -- Finalize the needed docs, forms and printables for asset collection. Be stern on the nature of the installation profiles and making executive choices soon so that purchasing can be done. Follow up with facilities on my requested dates. Once the process for asset collection is finalized, I can "dot an i" on the equipment/software listing I need for the project.

[phantomtutor]

Design an acceptable use policy for a software company that creates online advertising tailored to individuals based on the subjects they input into various search engines. Keep in mind that the employees of such a company would need unlimited access to the Internet. Make sure you are following the guildlines that have been set. Your name and Course should be in the heading of every page. Correct Punctuation and Grammer. Full complete sentences. Each paragragh should have at lease 3 sentence. ORDER THIS PAPER NOW. 100% CUSTOM PAPER CategoriesEducation homework help Leave a Reply Cancel replyYour email address will not be published. Required fields are marked *Comment * Name * Email * Website Save my name, email, and website in this browser for the next time I comment. Post navigation Previous PostPrevious Chapters 8-9 Discussion 99 unread replies.99 replies. Read Moore C. 8-9; Post YONext PostNext Concisely describe the process for the IRB prescreening review at Chamberlain Un

[keysolutionsinc-blog]

eProtocol | IRB System | Key Solutions

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In a rare, groundbreaking decision, Linux kernel project maintainers have imposed a ban on the University of Minnesota (UMN) from contributing to the open-source Linux project.

The move comes after a group of UMN researchers were caught submitting a series of malicious code commits, or patches that deliberately introduced security vulnerabilities in the official Linux codebase, as a part of their research activities.

Additionally, the Linux kernel project maintainers have decided to revert any and all code commits that were ever submitted from an @umn.edu email addresses.

[...]

The developer's justification for taking this step is:

"Commits from @umn.edu addresses have been found to be submitted in 'bad faith' to try to test the kernel community's ability to review 'known malicious' changes."

"Because of this, all submissions from this group must be reverted from the kernel tree and will need to be re-reviewed again to determine if they actually are a valid fix."

"Until that work is complete, [we are removing] this change to ensure that no problems are being introduced into the codebase," said Kroah-Hartman in a series of published emails.

In February 2021, UMN researchers published a research paper titled, "Open Source Insecurity: Stealthily Introducing Vulnerabilities via Hypocrite Commits."

The focus of this research was to deliberately introduce known security vulnerabilities in the Linux kernel, by submitting malicious or insecure code patches.

As seen by BleepingComputer, the researchers demonstrate many examples of instances where they introduced known vulnerabilities by making these "hypocrite" patch commits:

"Introducing the nullified state is straightforward. The patch is seemingly valid because it nullifies pf->disk->queue after the pointer is released."

"However, some functions such as pf_detect() and pf_exit() are called after this nullification and they would further dereference this pointer without checking its state, leading to NULL-pointer," state UMN researchers in their paper.

As seen by BleepingComputer, there are hundreds of commits touting themselves to be "patches" that have been reverted as a part of this process[.]

Soon enough, researcher Aditya Pakki from UMN pushed back asking Kroah-Hartman to refrain "from making wild accusations that are bordering on slander." Pakki wrote:

“Greg,

I respectfully ask you to cease and desist from making wild accusations that are bordering on slander.

These patches were sent as part of a new static analyzer that I wrote and it's sensitivity is obviously not great. I sent patches on the hopes to get feedback. We are not experts in the linux kernel and repeatedly making these statements is disgusting to hear.

Obviously, it is a wrong step but your preconceived biases are so strong that you make allegations without merit nor give us any benefit of doubt. I will not be sending any more patches due to the attitude that is not only unwelcome but also intimidating to newbies and non experts.”

To which Kroah-Hartman responded that the Linux kernel developer community does not appreciate being experimented on in this manner.

"If you wish to do work like this, I suggest you find a different community to run your experiments on, you are not welcome here," said Kroah-Hartman.

"Because of this, I will now have to ban all future contributions from your University and rip out your previous contributions, as they were obviously submitted in bad-faith with the intent to cause problems," he continued.

Last year, UMN researchers had compiled a detailed FAQ document in which they stated that the goal of this research was to improve the security of the patching process in open-source software by demonstrating the practicality of bug-introducing patches. 

The researchers also stated that any patch suggestions were made via email exchanges and never made it into any code branch, or the Linux kernel.

According to the document, the University's IRB determined that this was not human research or ethically harmful, and as such cleared the research activities. 

Although, the researchers did offer their sincere apologies to Linux maintainers for the time wasted on reviewing "hypocrite" patches:

"We would like to sincerely apologize to the maintainers involved in the corresponding patch review process; this work indeed wasted their precious time."

"We had carefully considered this issue, but could not figure out a better solution in this study," state the researchers. [...]