Health and Medicine
The Value of a Human Factors ProgramLocation: , United StatesCategory: Health and Medicine Start Date: 02-22-2018 Last Day: 02-23-2018 Deadline for abstracts: 02-20-2018 This seminar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.
The ISO 62366 is an "Consensus" Standard, making it a gold standard for regulatory submissions. We will look at other reference points regarding HF, like AAMI/ANSI HE75:2009 and how HF Engineering include consideration of:
Device Users
Use Environments and User Interfaces
Preliminary Analyses
Exploratory HF/Usability Evaluations
Hazard Mitigation and Control
We will look at the implication of HFE through Design Controls in the QSR:
Design input -includes "needs of the user and patient"
Design…
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Good Clinical Data Management Practices (GCDMP)Location: , United StatesCategory: Health and Medicine Start Date: 02-22-2018 Last Day: 02-23-2018 Deadline for abstracts: 02-20-2018 Why should you attend:
Good clinical data management (CDM) is paramount for a successful research. After all, Garbage In, Garbage Out (GIGO).
CDM is involved in all aspects of collecting, processing, and interpreting information. There are many types of computer applications and database systems to support data collection and management. However, there are elements of Good Clinical Practice that apply across the board.
Review and approval of drugs or devices by regulatory agencies requires the assumption that the data presented are valid and reliable. Integrity of the data is paramount to ensure confidence in the results and conclusions you will…
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Webinar On HIPAA Fundraising: What You Need to Know, What You Need to DoLocation: , United StatesCategory: Health and Medicine Start Date: 02-22-2018 Last Day: 02-22-2018 Deadline for abstracts: 02-21-2018 Training Options Duration: 60 Minutes
Thursday, February 22, 2018 | 10:00 AM PST | 01:00 PM EST
Overview: In 2013, The US Department of Health and Human Services made major changes to rules implementing The Health Insurance and Portability Act of 1996 (HIPAA) and Health Information Technology for Economic and Clinical Health Act of 2003 (HITECH). Among the many areas impacted by these rules (billing, marketing, research, IT security, etc.) is fund raising. The amendments significantly modify the methods and practice that hospitals, their institutionally related foundations, and other healthcare charities may or must employ when using ANY patient or…
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One Day of CardiotocographyLocation: , ItalyCategory: Health and Medicine Start Date: 02-23-2018 Last Day: 02-23-2018 Deadline for abstracts: 02-22-2018 Il corso si prefigge di fornire indicazioni aggiornate e complete in tema di cardiotocografia partendo dalla patofisiologia degli elementi che caratterizzano il tracciato fino alla gestione clinica delle anomalie che lo caratterizzano. Verranno esplicitate sia le procedure per la cosiddetta "rianimazione in utero" cioè il trattamento conservativo delle anomalie cardiotocografiche che quelle relative alle emergenze cardiotocografiche che prevedono la più rapida sottrazione del feto al rischio di acidosi.
Chiarezza verrà fatta in tema di classificazioni del tracciato cardiotocografico, sia confrontando le peculiarità delle diverse linee guida internazionali attualmente in uso, sia esponendo la recente classificazione italiana nata sotto l’egida della…
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Winter Wilderness First Aid Certification - ColoradoLocation: , United StatesCategory: Health and Medicine Start Date: 02-23-2018 Last Day: 02-25-2018 Deadline for abstracts: 02-23-2018 Students learn field herbal medicine for remote & off-grid situations of illness or injury with hands-on experience using clinical and role-playing based training in post-disaster scenarios.
Winter Wilderness Emergency First Aid Certification Training.
Students will learn an emphasis on field herbal medicine that can be realistically used in remote and off-grid situations of illness or injury with hands-on experience using clinical and role-playing based training in post-disaster scenarios. This is a 24 hour course taught over 3 days (8 hours per day) and includes both a conventional 16-Hour Wilderness First Aid (WFA) Certification through Emergency Care and Safety Institute (ECSI)…
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Taking Care Over the Long Haul: Improving Diabetes Management, Atlanta 2018Location: , United StatesCategory: Health and Medicine Start Date: 02-24-2018 Last Day: 02-24-2018 Deadline for abstracts: 02-24-2018 This CME-certified live program will help you address diabetes management in patient populations at high risk for diabetes and adverse diabetes-related health outcomes.
CCO is partnering with the American Association of Diabetes Educators and the Healthy Trucking Association of America to host 3 live continuing medical education meetings focusing on long haul truck drivers, a population at high risk for diabetes and adverse diabetes-related health outcomes. The first Saturday morning seminar will be held in Atlanta (Feb 24). This interactive seminar is CME-certified for 3.25 credits, and the target audience includes physicians (particularly DOT-certified physicians), physician assistants, and nurse practitioners.…
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HIPAA Compliance - Clear, Complete, Step-by-StepLocation: , United StatesCategory: Health and Medicine Start Date: 02-26-2018 Last Day: 02-27-2018 Deadline for abstracts: 02-25-2018 Organizations of all types and sizes continue to struggle needlessly with HIPAA Compliance. For example, HIPAA Risk Analysis - Risk Management is the basis of the HIPAA Compliance Program of every Covered Entity and Business Associate. But mandatory HIPAA Compliance Audits conducted by the Office for Civil Rights (OCR), the HIPAA enforcement arm of the U. S. Department of Health and Human Services (HHS), found 94% of Covered Entities failed the Risk Management Audit and 87% failed the Risk Analysis Audit. And every audited Covered Entity knew well in advance that it was on the short list to be audited,…
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Webinar On Conducting OSHA 300 Log Recordkeeping TrainingLocation: , United StatesCategory: Health and Medicine Start Date: 02-26-2018 Last Day: 02-26-2018 Deadline for abstracts: 02-25-2018 Training Options Duration: 90 Minutes
Monday, February 26, 2018 | 10:00 AM PST | 01:00 PM EST
Overview: OSHA has implemented a new online OSHA 300 Log Recordkeeping Reporting Requirement starting in June 2017. This has created a lot of questions and concerns from companies about what this requirement means and what OSHA will do with this information.
Why should you Attend: This course will give a comprehensive overview of what the new OSHA 300 Log Recordkeeping Reporting Requirements are so that a beginner or a seasoned EHS Professional will have confidence in knowing how to fill these out quickly…
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Webinar On Conducting OSHA 300 Log Recordkeeping TrainingLocation: , United StatesCategory: Health and Medicine Start Date: 02-26-2018 Last Day: 02-26-2018 Deadline for abstracts: 02-25-2018 Training Options Duration: 90 Minutes
Monday, February 26, 2018 | 10:00 AM PST | 01:00 PM EST
Overview: OSHA has implemented a new online OSHA 300 Log Recordkeeping Reporting Requirement starting in June 2017. This has created a lot of questions and concerns from companies about what this requirement means and what OSHA will do with this information.
Why should you Attend: This course will give a comprehensive overview of what the new OSHA 300 Log Recordkeeping Reporting Requirements are so that a beginner or a seasoned EHS Professional will have confidence in knowing how to fill these out quickly…
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Webinar On Texting and E-mail with Patients - Meeting Patient Requests within the HIPAALocation: , United StatesCategory: Health and Medicine Start Date: 02-26-2018 Last Day: 02-26-2018 Deadline for abstracts: 02-25-2018 Training Options Duration: 90 Minutes
Monday, February 26, 2018 | 10:00 AM PST | 01:00 PM EST
Overview: This session will focus on the rights of individuals to communicate in the manner they desire, and how a medical office can decide what is an acceptable process for communications with individuals. The session will explain how to discuss communications options with individuals so that you can best meet their needs and desires, while preserving their rights under the rules.
With the new HIPAA random audit program now getting under way, and increases in enforcement actions following breaches, now is the time…
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2018 Webinar On The Patient Experience: The Direct Path to Better Clinical OutcomesLocation: , United StatesCategory: Health and Medicine Start Date: 02-27-2018 Last Day: 02-27-2018 Deadline for abstracts: 02-26-2018 Training Options Duration: 60 Minutes
Tuesday, February 27, 2018 | 10:00 AM PST | 01:00 PM EST
Overview: If your current position requires that you engage directly with patients, that you respond or are responsible for HCAHPS outcomes, or you work with direct caregivers, this presentation will give you vital tools to optimize your own skills.We will look at the HCAHPS survey through systems thinking to make sense of how the questions influence each other. And, we will look at paths to improvement that are effective and sustainable over time.
Why should you Attend: The Patient Experience (PX) is the…
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Channel Optimization in Pharma Marketing 2018Location: , United StatesCategory: Health and Medicine Start Date: 02-28-2018 Last Day: 03-02-2018 With the rise of new patient engagement avenues and digital outlets, coupled with an increase in specialty drugs for a smaller patient population, a data-driven and targeted channel mix is crucial to commercial effectiveness.
The 2nd annual Channel Optimization in Pharma Marketing Summit unites Marketing and Business leaders from pharma and biotech organizations to evaluate the surge of innovations in the last 12 months - from a go-to-market strategy to technology utilization.
Join industry pioneers as they share their lessons learned.
URLs:
Booking: https://go.evvnt.com/187936-1?pid=154
Brochure: https://go.evvnt.com/187936-2?pid=154
Time: 09:00 to 18:00
Price:
Pharma Pricing: USD 1799,
Solution Provider Pricing: USD 2599…
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What is 21 CFR Compliance | 21 CFR Part 11 Regulations 2018Location: , United StatesCategory: Health and Medicine Start Date: 03-01-2018 Last Day: 03-02-2018 Deadline for abstracts: 03-01-2018 Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview:
Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and /…
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Drug Products for Clinical Trials | FDA Approved Drugs List 2018Location: , United StatesCategory: Health and Medicine Start Date: 03-01-2018 Last Day: 03-02-2018 Deadline for abstracts: 03-01-2018 In January 2006, FDA issued a final rule which specified that most pharmaceutical products (including biologics) produced for use in Phase I clinical trial studies were exempted from complying with GMP requirements, as defined in 21 CFR Part 211 under 21 CFR 210.2(c). Section 501(a)(2)(B) of the FD&C Act requires drugs, including IND products, to comply with cGMPs or if they are not manufactured in compliance with cGMPs, they are deemed adulterated. Based on this statutory requirement for manufacturers to follow GMPs, FDA issued cGMP regulations for drug and biological products in the Code of Federal Regulations (in 21 CFR…
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Medicare Marketing Do's and Dont'sLocation: , United StatesCategory: Health and Medicine Start Date: 03-01-2018 Last Day: 03-01-2018 Deadline for abstracts: 03-01-2018 OVERVIEW
Because the Anti-Kickback Statute is so broad it what it proscribes, healthcare organizations, conducting what would be normal marketing activities in other industries, have run afoul of the Statute on numerous occasions. The Statute and the regulations only tell part of the story. This program will review not only the Statute and its safe harbors, but will provide an in-depth overview of OIG guidance and advisory opinions dealing with marketing activities, as well as a review of case law regarding marketing behavior.
WHY SHOULD YOU ATTEND
If your organization, be it a hospital, physician practice, DME provider, or any…
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A Legal Compliance Program When Billing Durable Medical EquipmentLocation: , United StatesCategory: Health and Medicine Start Date: 03-01-2018 Last Day: 03-01-2018 Deadline for abstracts: 03-01-2018 OVERVIEW
Learn that treating your Medicare patients with Durable Medical Equipment can be great for patient clinical outcomes, a great revenue stream and can be legally compliant. It will also lower healthcare costs. However one must know how to get the proper licensure and know the Federal & State Guidelines.
WHY SHOULD YOU ATTEND
All practices are facing the fact their professional services reimbursements are shrinking from all insurance companies & especially Medicare. Patient loads are smaller due to the economy and operating costs are skyrocketing. Everyone needs to look at additional revenue opportunities with their own patient base while…
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Taking Care Over the Long Haul: Improving Diabetes Management, Dallas 2018Location: , United StatesCategory: Health and Medicine Start Date: 03-03-2018 Last Day: 03-03-2018 CCO is partnering with the American Association of Diabetes Educators and the Healthy Trucking Association of America to host 3 live continuing medical education meetings focusing on long haul truck drivers, a population at high risk for diabetes and adverse diabetes-related health outcomes. This interactive seminar is CME-certified for 3.25 credits, and the target audience includes physicians (particularly DOT-certified physicians), physician assistants, and nurse practitioners. Featuring case-based discussions with expert panelists, the agenda will focus on setting optimal glycemic targets, safely intensifying diabetes treatment, managing comorbid cardiovascular risk factors, and risk assessment. For more information and to register, go to…
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Taking Care Over the Long Haul: Improving Diabetes Management, Dallas 2018Location: , United StatesCategory: Health and Medicine Start Date: 03-03-2018 Last Day: 03-03-2018 Deadline for abstracts: 03-03-2018 CCO is partnering with the American Association of Diabetes Educators and the Healthy Trucking Association of America to host 3 live continuing medical education meetings focusing on long haul truck drivers, a population at high risk for diabetes and adverse diabetes-related health outcomes. This interactive seminar is CME-certified for 3.25 credits, and the target audience includes physicians (particularly DOT-certified physicians), physician assistants, and nurse practitioners. Featuring case-based discussions with expert panelists, the agenda will focus on setting optimal glycemic targets, safely intensifying diabetes treatment, managing comorbid cardiovascular risk factors, and risk assessment. For more information and to register, go to…
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2018 Course On how to Prepare for a HIPAA AuditLocation: , United StatesCategory: Health and Medicine Start Date: 03-06-2018 Last Day: 03-06-2018 Deadline for abstracts: 03-05-2018 Training Options Duration: 90 Minutes
Tuesday, March 6, 2018 | 10:00 AM PST | 01:00 PM EST
Overview: Being in compliance with HIPAA involves not only ensuring you provide the appropriate patient rights and controls on your uses and disclosures of protected health information, but you also have the proper policies and procedures in place. If audited or the subject of a compliance review you will be required to show the government you have all the necessary documentation in place for safeguarding patient Protected Health Information and indicate how you addressed all required security safeguards. This starts with the understanding…
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Recent Updates of FDA 21 CFR 11 Add-On InspectionsLocation: , United StatesCategory: Health and Medicine Start Date: 03-07-2018 Overview:
This presentation will cover the scope, status and results of the surveillance inspections and what they may mean for the future of 21 CFR Part 11. This will enable you to determine whether your company is subject to the most common violations so you can take action to have a better inspection outcome.
Why should you Attend:
In December 2010 the FDA changed the way it does audits to include 21 CFR 11 add-on inspections. Very little is known about this, yet the FDA has already issued citations on the subject.
Areas Covered In the Session:
What is FDA's…
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