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- Time:
- 3:00pm
- Description:
- The Institute for HealthCare Consumerism (IHC) and hCentive, have teamed up to co-create a webinar that will arm brokers with the knowledge necessary to navigate this burgeoning digital age of benefits technology.
Part one of the webinar series was focused on educating brokers on “winning during this Digital Revolution.” This included how to find the best-fit technology for you and your clients, what selling opportunities exist with a benefits technology, and streamlining what you do as a broker for better efficiency. We also heard from the Cypress Exchange on why they chose to adopt a benefits marketplace and how they’re leveraging for long-term growth and success.
In part two of the webinar series we will address the following:
Educating and training brokers and agents in technology adoption
Engaging your clients with a benefits marketplace for growth and retention
Creating marketing opportunities for your agency and field force
- Time:
- 8:00pm-8:40pm
- Description:
- Steps Your Business Can Take to Mitigate the Risks and Ensure a Smooth Transition to The Cloud
This webinar is for executives who are serious about cloud computing, but are unsure of how to securely and efficiently make the transition.
We've done the reseach for you.
When researching cloud options, it's important to understand the risks, bottlenecks, and productivity traps of moving to a cloud computing provider.
During this webinar, you'll learn:
1.The Signs It’s Time To Migrate To The Cloud
2.Steps To Managing Cloud Expectations
3.How to Identify & Mitigate the Cloud Risks
4.How to Ensure a Smooth Transition To The Cloud
(If you're a cloud computing beginner, you may want to start with our 'Cloud Computing 101' webinar)
- Time:
- 11:00pm-12:00am
- Description:
- Learn new skills to master the various challenges associated with living with a chronic medical condition. Learn how to take charge of your healthcare and self-care. Discover new ways to give your life meaning and purpose, and explore how to best adapt to changes and losses.
This webinar series provides the road map that will guide you in how to increase wellbeing despite health challenges. By engaging in the mindfulness-based practices presented in these webinars, which were developed out of new advances in psychology, you will learn that the power to be the master of your condition and your life is in your own hands.
Each chapter focuses on a tool to cultivate wellbeing and ends with helpful hints on medical self-efficacy.
This educational webinar series will inform you of evidence-based tools developed from recent advances in psychology. To increase mastery wellbeing, self-care & your ability to work collaboratively & proactively with yon partnership with your doctors.
- Description:
- Industry: Biotechnology , Medical Device , Pharmaceutical
Speaker: Robert J. Russell
Wednesday May-4-2016 01:00 PM | 02:30 PM - EDT
DESCRIPTION
This 90 minute webinar will help you gain a detailed overview of ICH GMPs and the nuances and differences between requirements in the US, EU and Japan. It will help prepare you for regulatory inspections in these countries.
Why Should You Attend?
This ICH GMP training course will provide your company the opportunity for a detailed overview of ICH GMP and the nuances and differences between the three main ICH triumvirate regions (U.S. EU and Japan).It will cover the key areas of how ICH was established, it's goals and objectives, expectations of the healthcare authorities involved and practical differences that you will experience in a GMP inspection of a facility by FDA, an EU Competent Authority or PMDA.
Areas Covered in the Seminar :
US, EU, Japan GMP Requirements(Practical ICH Area Differences, Healthcare Authority Inspection Focus)
I . U.S., EU and Japan GMPs - Status of Harmonization and Where We're Heading
Current efforts to further harmonize GMP requirements
Future expectation & likely progress
II . Where Inconsistencies Become a Problem: WHO, ICH, Countries
Flexibility in global expectations
Most challenging topics where alignment varies
III . Key Chapter Reviews
ICH GMP organization
Category reviews
IV . Compliance with ICH Guidelines for GMPs
Understanding and Insight into Healthcare Authority expectations
How GMP requirements / inspections can differ with a single ICH Standard
How regulators (from 3 regions) will assess / enforce compliance with Q7
V . GMP Comparisons for APIs
Auditing API facilities
Typical audit agenda
ICH Area differences
VI . GMP Comparisons for Finished Products
Auditing finished product facilities
Typical audit agenda
ICH Area differences
VII . GMP Comparisons for :
Excipients
Sterile products
Biologics
Clinical Packaging
VIII . Differences on Area GMP Inspections
Differences on how GMP inspections are conducted
Areas of GMP inspection focus by area
Modifying your self-inspection systems to customized area concerns
IX . Outsourcing Management. A Regional Perspective on:
Contract manufacturing
Contract packaging.
3 rd Party Contract testing
X . Auditing Your Facilities for Global Considerations
Importance of pre-audits to regional GMP focus.
How to focus your internal audits to a US, EU and Japan compliance system.
Who Will Benefit:
This Webinar will provide valuable assistance to all License Owner personnel in the Pharmaceutical, Biotechnology and Combination Products areas, including contract manufacturers, packagers and suppliers. Particular functional expertise receiving value from attending would be:
Manufacturing
Quality Assurance
Senior management
Project Managers
Qualified Persons (QPs)
Regulatory Compliance
CMC Personnel
Packaging Experts
Auditors and Staff
Consultants
Webinar Includes:
Q/A Session with the Expert to ask your question
Handouts (PDF print only copy of PowerPoint slides)
90 Minutes Live Presentation
Certificate of Attendance
- Description:
- Date: 4th May, 2016
Webinar Agenda:
A brief introduction to the SDN & NFV world
What value does SDN and NFV provide to operators ?
Focus areas of telecom operators and vendors
What are the challenges for telecom operators ?
How to manage telecom assets ?
Best practices of Resource Lifecycle Management in SDN & NFV world.
- Time:
- 5:00pm-6:30pm
- Description:
- DESCRIPTION
This session will review the requirements and current issues pertaining to mobile devices and present ways for the attendees to consider how to meet patient desires and stay within the regulations, including processes for managing portable devices, policies needed for ensuring secure communications and storage where needed, and procedures for meeting and documenting patient requests.
The session will explain the HIPAA regulations that apply to the use of portable devices, both as tools for staff to use, and as a means of communication with patients. Proper use of portable devices requires consideration of a variety of purposes: for personal use, for business use not involving any identifiable patient information, for business use that does involve identifiable patient information, and for communications with patients. Each type of use requires careful consideration of the rules and the risks to the confidentiality, integrity, and availability of information.
For business uses with no patient information, the constraints are few, so long as you are sure there is no patient information involved with those uses, But if you include any patient information, you need to ensure the information is protected. Even so, patients are allowed to ask to communicate with you in any way you can reasonably handle. Just what is reasonable and what is allowed according to guidance from HHS is discussed.
Once patient information is involved, the devices used by a provider or their staff must be properly secured through the use of good pass codes and encryption with remote wiping of data if lost or stolen, and if you allow staff to use their own devices for business work, what happens when they trade in their old phone when the new one comes out?
If you communicate with patients using portable devices, you need to consider the issues of privacy and security, as well as those of triaging incoming communications and documenting conversations. Just plain texting is not readily adaptable to the requirements of patient care and documentation, but secure, appropriate solutions are available.
Finally, we will discuss the enforcement of HIPAA rules and how they relate to mobile devices, the issues that can lead to enforcement, and the impacts of enforcement actions, including monetary settlements and corrective action plans.
Why should you attend :
The HIPAA regulations require the use of the mode of communication requested by the individual, if the provider has the capability to reasonably do so, and also require the consideration of secure technologies for communications and storage of data. The result is that the use of portable devices by patients and staff can be complicated and requires careful consideration of the regulations, how the devices will be used and secured, and patient desires.
HHS compliance audit activity and enforcement penalties are both increased, especially in instances of willful neglect of compliance, if, for instance, your organization hasn’t adequately considered the impact of mobile devices on your compliance. Given that mobile devices are a leading source of breaches of PHI, it is essential to consider these devices and how their use affects the privacy and security of PHI; not doing so is inviting enforcement action by HHS.
Areas Covered in the Session:
Presentation and explanation of regulatory requirements, typical situations, and appropriate responses to patient communications requests to develop understanding of the rules surrounding patient communications and access of information under HIPAA.
Presentation of information security issues related to communications and the risks associated with insecure communications, so you can know how to explain the risks of insecure communications to patients.
Discussion of policies and procedures for managing and auditing the use of insecure communications including communications made at the request of patients.
Presentation of requirements for encryption according to best practices
Explanation of technologies that can provide such encryption and security, to help you know when secure communications are required and what must be done to secure communications and devices.
Learn about the training and education that must take place and be documented to ensure your staff uses portable health information properly and does not risk exposure of PHI."
Who will benefit: (Titles)
Compliance director
CEO
CFO
Privacy Officer
Security Officer
Information Systems Manager
HIPAA Officer
Chief Information Officer
Health Information Manager
Healthcare Counsel/lawyer
Office Manager
Contracts Manager
Webinar includes:
Q/A Session with the Expert to ask your question
PDF print only copy of PowerPoint slides
90 Minutes Live Presentation
Certificate of attendance
For Registration : http://c2gowebinars.com/product/?topic=mobile-devices-hipaa
Note: Use coupon code <T9AIO8AY > and get 15% off on registration.
- Time:
- 2:00pm-3:00pm
- Description:
- This teleseminar is designed for Moms whose child has left home. This is a time of great change! this Teleseminar will provide support and ideas about how you can use this unique transition to thrive in your personal growth.