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E Signature Document Workflow

Healthcare Admin Director

Knowledge Graph Entities
Dominant · Search Engine Appearances ρ=0.492

AI recommendation signal analysis across 227 domains for the Healthcare Admin Director persona in E Signature Document Workflow.

227Domains Tracked
Healthcare Admin Director_persona.report
EntityScore
IBM
60.0
Q129793
50.6
Microsoft
47.1
Adobe Premiere Pro
45.0
digital signature
40.0
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This report tracks how AI models and search engines recommend companies across 100 industries. If you want the same analysis run specifically against your own site and competitors, get in touch.

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About This Report

How to use this page

Persona view: this page is scoped to this persona's queries alone.
Use Case

Check your knowledge-graph footprint

Wikidata is the structured knowledge graph behind Wikipedia, search engines, and many AI systems. If the graph does not know a brand, machines have less to anchor an answer on. See which entities carry this segment's topics and brands, and whether its top domains have an entity at all.

How It's Calculated

Where the numbers come from

We scan every Wikidata entity record (labels, descriptions, property values) for this segment's topic phrases and brand hostnames. Entity records are short structured data, so counts run far smaller than article text. Coverage checks which entities claim each domain as an official website.

Overview

What's on this page

Top-entity charts, the full entity table, and a knowledge-graph coverage check for this segment's most LLM-recommended domains.

Segment Totals

Knowledge graph at a glance

How much of the Wikidata knowledge graph touches Healthcare Admin Director. Entity records are short structured data (labels, descriptions, property values), so these counts run far smaller than Wikipedia article text; what matters is which entities show up, not raw volume.

15K
Entities With Topic Matches
971
Entities Mentioning Brands
16K
Topic Phrase Matches
1,246
Brand Mentions
Top Domains

Knowledge graph coverage

Whether a Wikidata entity claims each of this segment's most LLM-recommended domains as its official website. A brand without an entity is invisible to systems that navigate the web through the knowledge graph.

13 of 25 top domains for Healthcare Admin Director have a knowledge-graph entity.

DomainKnowledge Graph EntityWikidata ID
docusign.comDocusignQ5287613
adobe.comAdobeQ11463
hellosign.comNot in the knowledge graph-
pandadoc.comPandaDocQ25324145
signnow.comSignNowQ7512523
adobesign.comNot in the knowledge graph-
formstack.comFormstackQ16838881
dropboxsign.comNot in the knowledge graph-
onespan.comOneSpanQ3552887
jotform.comJotformQ24959818
dropbox.comDropboxQ142539
airslate.comNot in the knowledge graph-
rightsignature.comRightSignatureQ18390423
signeasy.comNot in the knowledge graph-
box.comBoxQ4951483
mproactive.comNot in the knowledge graph-
foxit.comFoxitQ5477193
nintex.comNintexQ73125324
sertifi.comNot in the knowledge graph-
pandasign.comNot in the knowledge graph-
certinal.comNot in the knowledge graph-
panda.comNot in the knowledge graph-
signrequest.comNot in the knowledge graph-
getaccept.comGetAcceptQ138008542
signwell.comNot in the knowledge graph-
Wikidata

Top knowledge-graph entities

The entity records where Healthcare Admin Director's brands and topics appear. Brand Mentions is the more reliable single ranking here; broadly used phrases can surface large unrelated entities in the topic view. Blended merges the two on a log scale (brand mentions weighted higher, 0 to 100). Bars and entity names link to the record; entities with no label show their Wikidata ID. The table follows the selected view.


EntityBlendedBrand MentionsTopic Matches
IBM60.0360
Q12979350.6200
Microsoft47.1160
Adobe Premiere Pro45.0140
digital signature40.003
XAdES40.003
informed consent form40.003
The generic Informed Consent Service gICS®: implementation and benefits of a modular consent software tool to master the challenge of electronic consent management in research40.003
Adobe Creative Cloud39.8100
Q20790238.390
Adobe Acrobat Reader DC38.390
Adobe Sign38.390
Adobe36.580
Adobe After Effects34.670
Adobe Photoshop Lightroom34.670
Q1869869034.670
M-Files34.670
Microsoft SQL Server32.360
Laserfiche32.360
Adobe for Business32.360
PAdES31.702
electronic signature31.702
Elliptic Curve Digital Signature Algorithm31.702
Digital Signature Algorithm31.702
CAdES31.702
Digital signature forgery31.702
The “Open Letter”: Radiologists' Reports in the Era of Patient Web Portals31.702
Easy-to-Read Informed Consent Forms for Hematopoietic Cell Transplantation Clinical Trials31.702
Readability and Content Assessment of Informed Consent Forms for Phase II-IV Clinical Trials in China31.702
Ethical considerations for informed consent in infertility research: The use of electronic health records31.702
Patient and public attitudes towards informed consent models and levels of awareness of Electronic Health Records in the UK31.702
Comparison of participant information and informed consent forms of five European studies in genetic isolated populations31.702
Data Security, HIPAA Compliance: Steps to Prevent a Data Breach in Your Dental Practice31.702
Revision of the informed consent form for patients based on investigation of adverse events of mFOLFOX6 regimen31.702
Screening the use of informed consent forms prior to procedures involving operative dentistry: ethical aspects31.702
A randomized trial comparing concise and standard consent forms in the START trial31.702
Anonymization of DICOM electronic medical records for radiation therapy31.702
Are research participants truly informed? Readability of informed consent forms used in research.31.702
The definition of placebo in the informed consent forms of clinical trials.31.702
Parent-Reported Outcomes of a Shared Decision-Making Portal in Asthma: A Practice-Based RCT31.702
GCP compliance and readability of informed consent forms from an emerging hub for clinical trials31.702
Readability and Content Assessment of Informed Consent Forms for Medical Procedures in Croatia31.702
Are patient consent forms for research protocols easy to read?31.702
Recommendations for informed consent forms for critical care clinical trials31.702
Randomization to standard and concise informed consent forms: Development of evidence-based consent practices31.702
The Usability of Electronic Personal Health Record Systems for an Underserved Adult Population31.702
Health Literacy, Education Levels, and Patient Portal Usage During Hospitalizations31.702
Improved participants' understanding in a healthy volunteer study using the SIDCER informed consent form: a randomized-controlled study31.702
Comprehension and informed consent: assessing the effect of a short consent form31.702
VICO: Ontology-based representation and integrative analysis of Vaccination Informed Consent forms31.702
Awareness and Use of the After-Visit Summary Through a Patient Portal: Evaluation of Patient Characteristics and an Application of the Theory of Planned Behavior31.702
Implementation of Certified EHR, Patient Portal, and “Direct” Messaging Technology in a Radiology Environment Enhances Communication of Radiology Results to Both Referring Physicians and Patients31.702
Refilling medications through an online patient portal: consistent improvements in adherence across racial/ethnic groups31.702
Readability of informed consent forms in clinical trials conducted in a skin research center31.702
Adapting comparative effectiveness research summaries for delivery to patients and providers through a patient portal31.702
Information sheets and informed consent forms for clinical study participants: towards standardised recommendations?31.702
Concern about security and privacy, and perceived control over collection and use of health information are related to withholding of health information from healthcare providers31.702
Impact of Patient Portal Secure Messages and Electronic Visits on Adult Primary Care Office Visits31.702
The adequacy of informed consent forms in genetic research in Oman: a pilot study31.702
Readability and comprehensibility of informed consent forms for clinical trials31.702
Informed Consent Form Challenges for Genetic Research in a Developing Arab Country with High Risk for Genetic Disease31.702
Understanding of Essential Elements Required in Informed Consent Form among Researchers and Institutional Review Board Members31.702
Social and Communicative Functions of Informed Consent Forms in East Asia and Beyond.31.702
Meaningful Use of a Confidential Adolescent Patient Portal31.702
SIDCER informed consent form: principles and a developmental guideline31.702
Informed Consent-Uninformed Participants: Shortcomings of Online Social Science Consent Forms and Recommendations for Improvement31.702
Improved participants' understanding of research information in real settings using the SIDCER informed consent form: a randomized-controlled informed consent study nested with eight clinical trials31.702
Improved pregnant women's understanding of research information by an enhanced informed consent form: a randomised controlled study nested in neonatal research31.702
"I understood…but some parts were confusing and hard to grasp": Patients′ perception of informed consent forms and clinical trials in Eldoret, Kenya31.702
Digital signatures and the electronic health records: providing legal and security guarantees31.702
Electronic signatures, digital signatures, and digital certificates31.702
Modifying a standard industry clinical trial consent form improves patient information retention as part of the informed consent process31.702
Informed consent and hospital consent forms: paper chasing in a video world31.702
An Analysis of UCNS Certified Headache Center Patient Intake Forms31.702
An efficient forward-secure group certificate digital signature scheme to enhance EMR authentication process31.702
Are informed consent forms that describe clinical oncology research protocols readable by most patients and their families?31.702
Informed consent and consent forms.31.702
Naming it 'nano': Expert views on 'nano' terminology in informed consent forms of first-in-human nanomedicine trials31.702
Evaluating the Readibility of Informed Consent Forms Available Before Anaesthesia: A Comparative Study.31.702
Hospital chief was right to release patient consent forms to media31.702
Informed consent in medical research. In routine practice the consent form is a request form and informed consent is informed choice31.702
Informed consent in medical research. Studies with important conclusions but without patient consent should be published.31.702
Informed consent in medical research. Doctors are arrogant to think they need to debate issue of patient consent31.702
Consent, Informed Consent and the Consent Form31.702
Understanding of Technical Terms and Contents of Informed Consent Forms for Sedative Gastrointestinal Endoscopy Procedures31.702
Impact of the systematic use of the informed consent form at public dental care units in Galicia (Spain).31.702
Personality, sex of participant, and face-to-face interaction affect reading of informed consent forms.31.702
Evaluation of the ability of clinical research participants to comprehend informed consent form31.702
Readability of pediatric biomedical research informed consent forms31.702
Consent forms as part of the informed consent process: moving away from "medical Miranda".31.702
Development of tool for the assessment of comprehension of informed consent form in healthy volunteers participating in first-in-human studies.31.702
The written informed consent form (WICF): factors that interfere with acceptance31.702
Readability of informed consent forms for research in a Veterans Administration medical center31.702
Contents and readability of currently used surgical/procedure informed consent forms in Nigerian tertiary health institutions31.702
RFC 3126: Electronic Signature Formats for long term electronic signatures31.702
A written consent form dating back to 1524 in Bursa Şer’iye (Sharia Court) records and a proposal of a new start date for consent forms31.702
Complaint alleges many deficiencies in IRB-approved informed consent form.31.702
Perception of the informed consent form by participants in clinical trials31.702
Assessing the benefit of a personalized EHR-generated informed consent in a dental school setting31.702
Informed consent and the readability of the written consent form31.702
Can we make informed consent forms more informative?31.702
Readability of informed consent forms for whole-exome and whole-genome sequencing31.702
Informed consent forms for clinical and research imaging procedures: how much do patients understand?31.702
Ethics in clinical research: Need for assessing comprehension of informed consent form?31.702
Evaluation of Patient Feedback following Laparoscopic Cholecystectomy based on Information Described in the Informed Consent form Developed by the Association of Polish Surgeons31.702
How Does the Patient React After Reading the Informed Consent Form of a Gynecological Surgery? A Qualitative Study31.702
Patient activation and use of an electronic patient portal31.702
Patient Recall of Informed Consent at 4 Weeks After Total Hip Replacement With Standardized Versus Procedure-Specific Consent Forms31.702
When do you need an informed consent form?31.702
Readability of informed consent forms for use with iodinated contrast media31.702
Electronic Communication of Protected Health Information: Privacy, Security, and HIPAA Compliance31.702
Disclosure of HIV status on informed consent forms presents an ethical dilemma for protection of human subjects31.702
Comprehensibility of patient consent forms for radiation therapy of cervical cancer31.702
A risk-specific anesthesia consent form may hinder the informed consent process31.702
Decisional incapacity and delirium in the critically ill: what is the real value of the informed consent form?31.702
Documenting informed consent for treatment with neuroleptics: an alternative to the consent form31.702
Use, content, and readability of written informed consent forms for treatment31.702
Easy-to-Read Informed Consent Form for Hematopoietic Cell Transplantation Clinical Trials: Results From BMT CTN 1205 Study31.702
'Universal' patient consent form for case reports.31.702
Commentary on "Electronic Communication of Protected Health Information: Privacy, Security, and HIPAA Compliance".31.702
Federal agency's final rule says informed consent forms must be dated31.702
Power, advocacy, and informed consent forms31.702
Evidence-Based Strategies for Shortening Informed Consent Forms in Clinical Research31.702
The two-part consent form: A suggestion for promoting free and informed consent31.702
The big Cs of the informed consent form: compliance and comprehension31.702
Use of a simplified consent form to facilitate patient understanding of informed consent for laparoscopic cholecystectomy.31.702
Vaccination Informed Consent Ontology31.702
The Quality of Informed Consent Forms-a Systematic Review and Critical Analysis.31.702
Assessment of a shortened informed consent form for pediatric research: a pilot study31.702
An Analysis of Informed Consent Form Readability of Oncology Research Protocols31.702
Trends of Informed Consent forms for industry-sponsored clinical trials in rheumatology over a 17-year period: Readability, and assessment of patients' health literacy and perceptions31.702
Global analysis of the readability of the informed consent forms used in public hospitals of Spain31.702
The radiology informed consent form: recommendations from the European Society of Cardiology position paper31.702
Patient information through informed consent form31.702
Introduction of an accreditation system for hospital informed consent forms31.702
Quality and legibility of written informed consent form in pharmacogenetic research31.702
Do patients understand what we explain to them in Informed Consent forms?31.702
Preoperative medical record-keeping can be improved: new informed consent form assists both physicians and patients31.702
Evaluation of the written informed consent form in clinical trials31.702
Effective Dose of PET/CT in Informed Consent Forms31.702
Informed consent forms fail to reflect best practice31.702
Low quality and lack of clarity of current informed consent forms in cardiology: how to improve them31.702
A new informed consent form model for cancer patients: preliminary results of a prospective study by the Italian Association of Medical Oncology (AIOM)31.702
Are informed consent forms for organ transplantation and donation too difficult to read?31.702
Series: for attending physicians: professionalism; informed consent forms as a dimension of medical communication31.702
Collection, storage, and allogeneic use of cord blood: informed consent form used by the italian biobank network31.702
Use of a low-literacy informed consent form to improve women's understanding of tubal sterilization: a randomized controlled trial31.702
The contents and readability of informed consent forms for oncology clinical trials31.702
Quality evaluation of informed consent forms: a pilot study31.702
Critical evaluation of informed consent forms for adult and minor aged whole blood donation used by United States blood centers31.702
All and part. Informed consent forms and clinical information procedure31.702
Are We Misjudging How Well Informed Consent Forms are Read?31.702
A template for informed consent forms in medical examination and treatment: an intervention study31.702
Doctor who changed patient consent form to cover up mistake is struck off31.702
eConsent31.702
What information and the extent of information research participants need in informed consent forms: a multi-country survey31.702
Evaluation of the readability of informed consent forms used in urology: Is there a difference between open, endoscopic, and laparoscopic surgery?31.702
When it comes to HIT, patience pays off. Patient consent forms enhance standardization, access for multispecialty clinic31.702
Readability of informed consent forms for subjects participating in biomedical research: updating is required31.702
IRB opts for "user friendly" letter rather than an informed consent form31.702
Consenting to ambiguities: a documental analysis of informed consent forms used in assisted human reproduction clinics31.702
Assessing patient comprehension of informed consent forms31.702
Readability of the informed consent form used in the Health Service of Asturias (Spain)31.702
An informed consent form for treatment with oral anticoagulants31.702
Concepts, categories, and value judgments in informed consent forms31.702
Informed consent forms in medical practice: the results of a knowledge survey31.702
Readability of education materials and informed consent forms for women seeking surgical sterilization31.702
Informed consent. Screening programmes need consent forms31.702
Testing for inherited susceptibility to breast cancer: A survey of informed consent forms for BRCA1 and BRCA2 mutation testing31.702
The legibility of written informed consent forms31.702
"Good friend" can sign informed consent forms31.702
Readability of written informed consent forms used in exercise and sport psychology research31.702
Development of a model angiography informed consent form based on a multiinstitutional survey of current forms31.702
Informed consent readability: subject understanding of 15 common consent form phrases31.702
Can your research subjects read your study's informed consent form?31.702
The effect of an introduction of a new consent form on settlement of the doctrine "informed consent"31.702
Patient consent/informed consent31.702
Evaluating the readability of informed consent forms used in contraceptive clinical trials31.702
Informed consent in the regional hospital of Japan--with a particular reference to consent forms31.702
Readability of informed consent forms31.702
Patient consent form for recording consultations31.702
Informed consent vs. consent forms31.702
Informed consent and consent forms31.702
A consent form for informed consent31.702
Failure to secure informed consent--necessary elements of proof--emergency situations; consent form--contents--prima facie evidence--failure to use31.702
Public health and the law. Informed consent and blanket consent forms31.702
Patient consent form--a prototype for Candadian hospitals31.702
Patient consent form31.702
Informed Consent Forms in Oncology Research: Linguistic Tools Identify Recurrent Pitfalls31.702
Patient Portal - Flu Reminder Recall31.702
Modified Consent Form Utility31.702
Patients' Readings of Pre-operative Informed Consent Forms31.702
Sensor and Electronic Health Records (EHR) Integration Pilot Study31.702
A Survey on Including Risks in the New "Key Information" Section of an Informed Consent Form31.702
Do Patients Participating In Oncology Clinical Trials Understand the Informed Consent Form?31.702
Patient Portal Reminder/Recall for Influenza Vaccination in a Health System- RCT 231.702
Development of a comprehensive community pharmacy patient intake form compliant with OBRA'90 requirements31.702
Patient portal in your orthopedic surgery practice: you can so do this31.702
Optimize your patient portal31.702
RISK MANAGEMENT STRATEGIES FOR PATIENT PORTAL USE31.702
Evaluation of Legal Legislation Compliance and Readability of Clinical Trial Informed Consent Forms31.702
Informed Consent Form Challenges for Genetic Research in Jordan31.702
Some researchers wear yellow pants, but even fewer participants read consent forms: Exploring and improving consent form reading in human subjects research31.702
Does content of informed consent forms make surgeons vulnerable to lawsuits?31.702
Improved parental understanding by an enhanced informed consent form: a randomized controlled study nested in a paediatric drug trial31.702
Assessment of Use, Specificity, and Readability of Written Clinical Informed Consent Forms for Patients With Cancer Undergoing Radiotherapy31.702
Implementation of Common Rule Changes to the Informed Consent Form: A Research Staff and Institutional Review Board Collaboration31.702
[Analysis of documented informed consent forms for computed tomography : Completeness and data quality in four clinics]31.702
Evaluation of Legal Legislation Compliance and Readability of Clinical Trial Informed Consent Forms31.702
Impact of Patient Use of an Online Patient Portal on Diabetes Outcomes31.702
Assessment of the quality of Patient Information Sheets and Informed Consent Forms for clinical trials at a Hospital Neurology Service31.702
Assessing Parent Decisions About Child Participation in a Behavioral Health Intervention Study and Utility of Informed Consent Forms31.702
Informed surgical consent during the COVID-19 pandemic: Exploring the risk of unknown-Update of informed consent form31.702
Patient Consent Management by a Purpose-Based Consent Model for Electronic Health Record Based on Blockchain Technology31.702
Clinical investigation and informed consent form in times of COVID-19 pandemic. A vision from the comitee ethics of research31.702
Is There a Difference Between the Readabilities of Informed Consent Forms Used for Elective and Emergency Procedures in Turkey?31.702
Redesign of an informed consent form to increase participation in a school-based dental program31.702
RSA releases free digital signature software31.702
The readability of informed consent forms for research studies conducted in South Africa31.702
Informed consent forms for gynecologic cancer surgery: recommendations from the Korean Society of Gynecologic Oncology31.702
Readability of Participant Informed Consent Forms and Informational Documents31.702
Is There a Difference Between the Readabilities of Informed Consent Forms Used for Elective and Emergency Procedures in Turkey?31.702
A survey on the current status and future perspective of informed consent management in the MIRACUM consortium of the German Medical Informatics Initiative31.702
Clinical investigation and informed consent form in times of COVID-19 pandemic. A vision from the comitee ethics of research31.702
INFORMED CONSENT FORM: CONCEPTS THAT THE ULTRASONOGRAPHIST SHOULD KNOW31.702
Quality of written informed consent forms for electroconvulsive therapy in Australia: a comparative analysis31.702
Examination of Informed Consent Forms in Masters and Doctorate Theses of Educational Sciences31.702
Readability of Pediatric Biomedical Research Informed Consent Forms31.702
Readability of the informed consent forms in Flanders using the Douma index: Analyzing the documents that help patients make decisions31.702
Characterization of Informed Consent Forms Posted on ClinicalTrials.gov31.702
Development, piloting, and evaluation of an evidence-based informed consent form for total knee arthroplasty (EvAb-Pilot): a protocol for a mixed methods study31.702
Informed consent forms for gynecologic cancer surgery: recommendations from the Korean Society of Gynecologic Oncology31.702
Virtual consent and the use of electronic informed consent form in clinical research in Brazil31.702
Consent, informed consent and the consent form31.702
Patch test informed consent form: position statement by European Academy of Dermatology and Venereology Task Force on Contact Dermatitis31.702
Usage of informed consent form for Bee-venom pharmacopuncture Therapy at korean medicine hospitals and Proposal for development of a standard informed consent form.31.702
A Consent Form Does Not Informed Consent Make31.702
Comprehensibility Levels of Informed Consent Forms in a State Hospital Internal Medicine Clinic: A Descriptive Study31.702
Informed Consent for Online Research—Is Anybody Reading?: Assessing Comprehension and Individual Differences in Readings of Digital Consent Forms31.702
Use, content, and readability of written informed consent forms for treatment.31.702
Current Status and Issues of Informed Consent Forms from the Quality Standards of Decision Aid:Including Interviews with Stakeholders31.702
Informed Consent - G.R. Morrow, How Readable Are Subject Consent Forms?, Journal of the American Medical Association 244(1): 56–58 (July 4, 1980) [8-1475].31.702
Readability of informed consent forms for research in a Veterans Administration medical center31.702
GWMAB collection of consent forms31.702
Patient Portal Flu Vaccine Reminders_RCT 431.702
Continuous quality improvement: reducing informed consent form signing errors31.702
Do Our Patients Read Informed Consent Forms?31.702
Improvement of Informed Consent Document Management in Clinical Trials Using an Electronic Medical Record System31.702
A Model for Implementing an Interoperable Electronic Consent Form for Medical Treatment Using HL7 FHIR31.702
Is There a Difference Between the Readabilities of Informed Consent Forms Used for Procedures in the Emergency Services of State and University Hospitals in Turkey?31.702
Evaluation of the Readability of Informed Consent Forms Used for Emergency Procedures31.702
Amendment of informed consent forms in the cardiovascular surgery in accordance with recent regulation on patient rights and legal responsibility of cardiovascular surgeons31.702
Translating the consent form is the tip of the iceberg: using cognitive interviews to assess the barriers to informed consent in South African health facilities31.702
A postal informed consent form for upper gastrointestinal endoscopy31.702
Leveraging semantic context to establish access controls for secure cloud-based electronic health records31.702
Q13592374731.702
Q13592383431.702
Obtaining meaningful informed consent: preliminary results of a study to develop visual informed consent forms with children31.702
AllSign31.702
Holosign31.702
SuperSign31.702
SignNow31.511
OnBase Cloud31.511
jSign31.511
pdfFiller31.511
Media Creation Tool29.850
Data Analytics for Machine Learning29.850
Q8068926.740
Adobe Flash Player26.740
Microsoft Lumia 640 XL26.740
Jotform26.740
Nintex26.740
ContractSafe26.740
Microsoft Windows23.030
Adobe Audition23.030
IBM Bluemix23.030
Microsoft Lumia 64023.030
Microsoft Docs23.030
Microsoft Learn23.030
Microsoft Typography23.030
Concord23.030
Rotterdam Convention20.001
encryption20.001
Xerox20.001
FIPS 20120.001
GNU Privacy Guard20.001
Electronic document management system20.001
records management20.001
LogicalDOC20.001
i-PIN20.001
certificate signing request20.001
informed consent20.001
document management system20.001
transaction log20.001
XML Signature20.001
audit trail20.001
health administration20.001
Lexmark20.001
advanced electronic signature20.001
identity verification20.001
Schnorr digital signature scheme20.001
GMR20.001
Goldreich-Goldwasser-Halevi signature scheme20.001
PDF/UA20.001
role-based access control20.001
NTRUSign20.001
Merkle signature scheme20.001
ODMA20.001
qualified electronic signature20.001
blind signature20.001
Rabin signature algorithm20.001
Certigreffe20.001
ISO 19005–1:2005: Document management—Electronic document file format for long-term preservation—Part 1: Use of PDF 1.4 (PDF/A-1)20.001
ISO 32000–1:2008: Document management—Portable document format—Part 1: PDF 1.720.001
document flow20.001
Retinal scan20.001
vulnerable population20.001
Kimios20.001
Xambox20.001
microfilmer20.001
FIPS 186 Digital Signature Standard20.001
GOST R 34.10-201220.001
ABA digital signature guidelines20.001
Boneh–Lynn–Shacham20.001
business process automation20.001
CA-720.001
Chesapeake Regional Medical Center20.001
consent20.001
consent management20.001
Digital Signature Services20.001
electronic signatures and law20.001
Digital signature transponder20.001
Distributed Access Control System20.001
document automation20.001
eFileCabinet20.001
ETSWAP20.001
Electronic Signatures in Global and National Commerce Act20.001
Executive Technologies20.001
Exstream Software20.001
IBM Rational ClearQuest20.001
identity verification service20.001
Informed Consent20.001
involuntary euthanasia20.001
voter-verified paper audit trail20.001
James Caird Burt20.001
Korean Certificate-based Digital Signature Algorithm20.001
Lason20.001
Marc Twagirumukiza20.001
Mayan20.001
Mobile Electronic Signature Consortium20.001
OpenKM20.001
patient portal20.001
protected health information20.001
quantum digital signature20.001
Q726965220.001
Digital Signature Act 199720.001
SHSH blob20.001
ShareMethods20.001
Signatures with efficient protocols20.001
signing ceremony20.001
multi-factor authentication20.001
Unbalanced Oil and Vinegar20.001
WYSIWYS20.001
XPS Annotator20.001
Xpertdoc20.001
Yep20.001
Category:Digital signature schemes20.001
Category:Document management systems20.001
Category:Wikipedians by alma mater: La Trobe University - Electronic Health Records20.001
Q920844420.001
ICP-Brasil20.001
electronic health record20.001
Act on Certification Business of Local Governments in Relation to Electronic Signatures20.001
Act on Electronic Signatures and Certification Business20.001
Egyptian National Identity Card20.001
Digital Signature Act20.001
Signority20.001
Internet Journal of Healthcare Administration20.001
Digital Evidence and Electronic Signature Law Review20.001
Category:Digital signature20.001
Constructing digital signatures from a one-way function20.001
XML digital signatures20.001
Category:Electronic signature providers20.001
Digital signature in Estonia20.001
Edwards-curve Digital Signature Algorithm20.001
Jumio20.001
Free, prior and informed consent20.001
software token20.001
SQRL20.001
PARAMOUNT trial20.001
High-priority drug–drug interactions for use in electronic health records20.001
Electronic Signatures Directive20.001
Chinese researchers crack major U.S. government algorithm used in digital signatures20.001
Contentverse20.001
Act on Electronic Signatures20.001
Electronic Signatures Act20.001
PARAMOUNT Eli Lilly Informed Consent Document20.001
NIST Koblitz Curves Parameters20.001
Digital Document20.001
Fast Healthcare Interoperability Resources20.001
YubiKey20.001
Q1991188920.001
Catalan General Subdirectorate of Archives and Document Management20.001
GB Group20.001
FedRAMP20.001
How to Achieve a McEliece-Based Digital Signature Scheme20.001
ESign20.001
Ring learning with errors signature20.001
PeopleDoc20.001
Data too important to share: do those who control the data control the message?20.001
Assessing Healthcare Utilization for Influenza-like Illness at an Emergency Department and a Student Health Service during the 2009–2010 H1N1 Pandemic20.001
The Feasibility of Using Electronic Health Records to Describe Demographic and Clinical Indicators of Migrant and Seasonal Farmworkers20.001
Incorporating occupational information in electronic health records: letter report20.001
Use of electronic health records to support smoking cessation20.001
Audio-visual presentation of information for informed consent for participation in clinical trials20.001
Extended discussion of information for informed consent for participation in clinical trials20.001
Interventions to promote informed consent for patients undergoing surgical and other invasive healthcare procedures20.001
Use of electronic health records to support smoking cessation20.001
Use of electronic health records to support smoking cessation20.001
Interventions to promote informed consent for patients undergoing surgical and other invasive healthcare procedures20.001
Audio-visual presentation of information for informed consent for participation in clinical trials20.001
Data resource profile: cardiovascular disease research using linked bespoke studies and electronic health records (CALIBER)20.001
Informed consent in the genomics era20.001
ZertES20.001
QT interval and antidepressant use: a cross sectional study of electronic health records20.001
Eyes Wide Open: The Personal Genome Project, Citizen Science and Veracity in Informed Consent20.001
Improving the risk-benefit relationship and informed consent for patients treated with hydroxychloroquine20.001
Quality assessment of patient leaflets on misoprostol-induced labour: does written information adhere to international standards for patient involvement and informed consent?20.001
Informed consent20.001
Informed consent in embryonic stem cell research: are we following basic principles?20.001
Use of electronic health records in disaster response: the experience of Department of Veterans Affairs after Hurricane Katrina20.001
Validating drug repurposing signals using electronic health records: a case study of metformin associated with reduced cancer mortality20.001
The student and the ovum: the lack of autonomy and informed consent in trading genes for tuition20.001
Informed consent and research design in critical care medicine20.001
Optimizing the HIV/AIDS informed consent process in India20.001
Attitudes of the Japanese public and doctors towards use of archived information and samples without informed consent: preliminary findings based on focus group interviews20.001
Being uninformed on informed consent: a pilot survey of medical education faculty20.001
User Electronic Signature20.001
Pyrus20.001
Category:Standards for electronic health records20.001
BLISS signature scheme20.001
Category:Electronic health records20.001
ISO 19005–2:2011: Document management—Electronic document file format for long-term preservation—Part 2: Use of ISO 32000-1 (PDF/A-2)20.001
ISO 19005–3:2012: Document management—Electronic document file format for long-term preservation—Part 3: Use of ISO 32000-1 with support for embedded files (PDF/A-3)20.001
"Negotiorum Gestio" in Family Medicine, Informed Consent Obtainment, and Disciplinary Responsibility20.001
Utilizing electronic health records to predict acute kidney injury risk and outcomes: workgroup statements from the 15(th) ADQI Consensus Conference20.001
Evaluation of interventions for informed consent for randomised controlled trials (ELICIT): protocol for a systematic review of the literature and identification of a core outcome set using a Delphi survey20.001
Blue Button use by patients to access and share health record information using the Department of Veterans Affairs' online patient portal20.001
Patient Access to Electronic Health Records During Hospitalization20.001
Patients, care partners, and shared access to the patient portal: online practices at an integrated health system20.001
Let’s Show Patients Their Mental Health Records20.001
Patients Who Share Transparent Visit Notes With Others: Characteristics, Risks, and Benefits20.001
Patients learning to read their doctors’ notes: the importance of reminders20.001
Transparent Electronic Health Records and Lagging Laws20.001
Utilities of Electronic Medical Records to Improve Quality of Care for Acute Kidney Injury: Past, Present, Future20.001
Patient centric approach for clinical trials: Current trend and new opportunities20.001
Informed consent in clinical research: Consensus recommendations for reform identified by an expert interview panel20.001
Transforming Health Care Delivery Through Consumer Engagement, Health Data Transparency, and Patient-Generated Health Information20.001
The Use of Medical Scribes in Health Care Settings: A Systematic Review and Future Directions20.001
Aspects of vulnerable patients and informed consent in clinical trials20.001
Genetic data and electronic health records: a discussion of ethical, logistical and technological considerations20.001
Ethical governance in biobanks linked to electronic health records20.001
Electronic health records: new opportunities for clinical research20.001
Different aspects of informed consent in aesthetic surgeries20.001
Informed consent process for patient participation in rare disease registries linked to biorepositories20.001
Improving informed consent in percutaneous coronary revascularisation20.001
Patients' online access to their electronic health records and linked online services: a systematic interpretative review20.001
ISO/IEC 7942-3:1999: Information technology—Computer graphics and image processing—Graphical Kernel System (GKS)—Part 3: Audit trail20.001
Security and privacy in electronic health records: a systematic literature review20.001
Criteria for assessing high-priority drug-drug interactions for clinical decision support in electronic health records20.001
A review of the empirical evidence of the value of structuring and coding of clinical information within electronic health records for direct patient care20.001
Possibilities and Implications of Using the ICF and Other Vocabulary Standards in Electronic Health Records20.001
An Autism Case History to Review the Systematic Analysis of Large-Scale Data to Refine the Diagnosis and Treatment of Neuropsychiatric Disorders20.001
Is Informed Consent Broken?20.001
Informed consent comprehension in African research settings20.001
Stakeholder engagement: a key component of integrating genomic information into electronic health records20.001
Electronic health records: Implications for drug discovery20.001
Implementing electronic health records in hospitals: a systematic literature review20.001
Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics20.001
Q2702801220.001
A method for obtaining digital signatures and public-key cryptosystems20.001
OpenDocument Text, version 1.220.001
OpenDocument Spreadsheet, version 1.220.001
OpenDocument Presentation, version 1.220.001
OpenDocument Graphics, version 1.220.001
OpenDocument Database, version 1.220.001
A survey on patients' knowledge and expectations during informed consent for spinal surgery: can we improve the shared decision-making process?20.001
A survey of study participants' understanding of informed consent to participate in a randomised controlled trial of acupuncture20.001
Informed consent: do information pamphlets improve post-operative risk-recall in patients undergoing total thyroidectomy: Prospective randomized control study20.001
Clinical predictors of antipsychotic use in children and adolescents with autism spectrum disorders: a historical open cohort study using electronic health records20.001
Use of mobile devices and the internet for multimedia informed consent delivery and data entry in a pediatric asthma trial: Study design and rationale20.001
Improving the informed consent process in international collaborative rare disease research: effective consent for effective research20.001
Optimising recruitment and informed consent in randomised controlled trials: the development and implementation of the Quintet Recruitment Intervention (QRI).20.001
Visualization of Data Regarding Infections Using Eye Tracking Techniques20.001
Advancing Informed Consent for Vulnerable Populations20.001
Mining electronic health records: towards better research applications and clinical care20.001
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Dropbox18.320
Adobe Digital Editions18.320
Windows Glyph List 418.320
Windows Installer18.320
SPSS18.320
DirectX18.320
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Wolters Kluwer18.320
Microsoft Paint18.320
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CHKDSK18.320
Microsoft Digital Image18.320
Windows Registry18.320
Visual Basic for Applications18.320
Microsoft OneDrive18.320
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Microsoft AutoRoute18.320
Adobe LiveCycle Designer18.320
IBM Informix18.320
CICS18.320
IBM Rational DOORS18.320
Microsoft Virtual Server18.320
Adobe FrameMaker18.320
Telephony Application Programming Interface18.320
Rational Rhapsody18.320
IBM Power Systems18.320
CPLEX18.320
Microsoft Student18.320
Adobe LiveMotion18.320
Wolters Kluwer Deutschland18.320
Adobe Content Server18.320
Microsoft Layer for Unicode18.320
IBM Configuration Management Version Control18.320
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Adobe RoboHelp18.320
Adobe eLearning Suite18.320
athenahealth18.320
Box18.320
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Microsoft Search Server18.320
Q1098455618.320
Microsoft Pinyin IME18.320
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Microsoft Lumia 950 XL18.320
Windows Subsystem for Linux18.320
Adobe XD18.320
Microsoft Dynamics 36518.320
CaosDB - Research Data Management for Complex, Changing, and Automated Research Workflows18.320
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Microsoft Academic Graph18.320
Microsoft Saudi18.320
GetApp18.320
IBM Cloud18.320
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IBM Cloud Object Storage18.320
Medicai18.320
Microsoft Lists18.320
Microsoft Berlin18.320
Antimalware Scan Interface18.320
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oneview11.510
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ColdFusion Markup Language11.510
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Windows HPC Server 200811.510
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BootVis11.510
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Microsoft Keyboard Layout Creator11.510
Microsoft Software Licensing and Protection Services11.510
SQL Server Management Studio11.510
WebSphere Portal11.510
Windows CE 4.011.510
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Acrobat Distiller11.510
Adobe Font Development Kit for OpenType11.510
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Adobe Originals11.510
Adobe Ovation11.510
Adobe Pixel Bender11.510
Adobe Premiere Express11.510
Adobe Technical Communication Suite11.510
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User Mode Driver Framework11.510
Windows Phone11.510
Business Catalyst11.510
COM Structured Storage11.510
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