Skip to main content

Posts

Showing posts from January, 2018

How to Effectively Consult to Physicians and Healthcare Leaders on Compliance issues.

Compliance Key INC  -  Healthcare Training Online                                                   Jay Anstine Jay Anstine Keynote Speaker at Compliance key Inc . He is the President of Bluebird Healthlaw Partners, LLC. As a healthcare lawyer specializing in regulatory compliance, Mr. Anstine consults to physicians, senior management, and boards of directors on compliance programs and regulatory issues impacting operations. Mr. Anstine's professional background includes working on the provider and the payer side of the market, for large for-profit and non-profit health systems, and small physician-owned entities.  Webinar Id:   LSHCJH003    10:00 AM PT | 01:00 PM ET   02/05/2018  Duration: 60 mins  Overview This webinar is designed to provide strategies and insights for effectively consulting to physicians and healthcare leaders on compliance issues. It will cover how to think and act like a consultant, a consistent process for consulting and strategies for

HIPAA Breach - or Not? How to Find Out & What to Do

Compliance Key INC  -  HIPAA Webinar                                                Paul Hales Paul Hales is a Keynote Speaker at Compliance Key, Inc. He received his Juris Doctor degree from Columbia University Law School and is licensed to practice law before the Supreme Court of the United States.  Webinar Id:   HIPHPH010    10:00 AM PT | 01:00 PM ET   01/31/2018  Duration: 60 mins  Overview More than 170 million Americans have been affected by Breaches of Unsecured Protected Health Information (PHI) since 2009. A Ransomware attack that encrypts PHI is now presumed to be a HIPAA Breach by Federal regulators. HIPAA Breach Notification Content and Timeliness are 2 of the top Enforcement priorities of the Office for Civil Rights (OCR), the HIPAA enforcement arm of the U. S. Department of Health and Human Services. Why should you attend this webinar? Breaches of unsecured PHI is becoming more and more common. The question is not whether a Covered Entity or Bu

8 Ways to Reduce the Cost of Your RoHS/REACH Compliance Program

Compliance Key INC  -   Compliance Training                                                James Kandler Jim Kandler is Keynote Speaker at Compliance key Inc. He is a Managing Director of RoHS Ready LLC. We are a b2c consultant unlike any other you know. We can quickly apply our actionable expertise, enabling your product to be compliant, on-time and on budget.   Webinar Id:   CIFWJK001    12:30 PM PT | 03:30 PM ET   01/29/2018  Duration: 60 mins  Overview The Webinar will propose several practical methods a manufacturer might implement to make their material compliance efforts more effective. The material regulations are expanding and becoming more inclusive. These changes are increasing the negative impact of RoHS and REACH compliance on manufacturers. To mitigate increasing cost and risk there are several potential process enhancements that might be implemented by manufacturers. In this presentation 8 ideas for internal business functional improvements will

The Top 20 Controls to Detect and Prevent Fraud

Compliance Key INC  -  Online Compliance Training Solutions                                                   Chris Doxey Chris  is Keynote Speaker at Compliance key Inc. She held senior finance and controller positions at Digital Equipment Corporation, Compaq, and Hewlett Packard which allowed her to develop and implement standards of internal control and leading practices for all aspects of financial operations.  Webinar Id:   CIFCA002    10:00 AM PT | 01:00 PM ET    01/29/2018  Duration: 60 mins  Overview The "Top Twenty Internal Controls" to detect and fraud are built upon standards of internal control and risk management. This instructor will review each control in detail and will suggest the roles and responsibilities for each control. Specific examples will be given for each top twenty control including the top three critical corporate controls.  Why should you attend this webinar? Learn about internal control best practices. Learn about the

Pharmaceutical Quality Risk Management (QRM) Overview

Compliance Key INC  -  Enterprise Risk Management training                                                  STEVEN LAURENZ Steven Laurenz- Chemical Engineering M.S. - Michigan State University Expertise: Over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization.  Webinar Id:   LSHCST001  10:00 AM PT | 1:00 PM  ET   01/24/2018  Duration: 60 mins  Overview Per ICH Q10 Quality risk management is integral to an effective pharmaceutical quality system. It can provide a proactive approach to identifying, scientifically evaluating and Controlling potential risks to quality. However integrating the principles of QRM into our quality processes is complex especially in a pharmaceutical organization. There is much confusion on how to define risk and individuals often think of quality risk management as just a tool like FMEA analysis verses an overall QRM approach. This training will explain t

HIPAA Changes 2018: How to Comply

Compliance Key INC  -  HIPAA Compliance Training Seminar                                                 Brian L Tuttle Brian Tuttle is Keynote Speaker at Compliance key Inc . He is Certified Professional in Health IT (CPHIT), Certified HIPAA Professional (CHP), Certified Business Resilience Auditor (CBRA) with over 17 years experience in Health IT and Compliance Consulting. Mr. Tuttle has worked all of those 15 years with MAG Mutual Healthcare Solutions and is now Senior Compliance Consultant and IT Manager with InGauge Healthcare Solutions (previously named MAG Mutual Healthcare Solutions).  Seminar Id:  IJ2018S2  06:00 AM PT | 09:00 AM ET  02/16/2018  Duration 1 Day Overview This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid gloves any more.It will also address major changes under the Omnibus Rule and any other applicable up

IDMP: Data Collection

Compliance Key INC  -  Regulatory Compliance Training                                               Joel Finkle Joel Finkle is Director, Regulatory Innovation and IDMP Strategy for ACUTA. In this role he brings new technologies and regulatory data standards to ACUTA's bio/pharmaceutical customers to ensure compliance and process improvements.  Webinar Id:   LSHCJI001  12.30 PM PT | 03.30 PM ET   01/23/2018  Duration: 60 mins  Overview This session will review the basic requirements of the initial planned European implementation of the ISO IDMP standard, then explore how the data for a product could be gathered for entry into a RIM system or what is expected in the agency web portal. Benefits of integration in a RIM environment, and downstream use of the data, will be covered. Why should you attend this webinar? Compliance with IDMP is not expected for a couple years, but the amount of preparation for existing products is extensive. Getting ahead of the dead

Batch Production Record and Device History Record Review and Quality Assessment to ensure compliance with DMF and DMR specifications

Compliance Key INC  -   Medical Device Training                                                 Jerry Dalfors Jerry Dalfors is Keynote Speaker at Compliance key Inc .He has extensive (40+ years) of business administration, consultative, technical and managerial experience in the development and manufacture of highly regulated biopharmaceutical products including injectables, biologics, medical devices and oral dosages.  Webinar Id:   LSHCJB002  12:30pm PT | 03:30pm ET   01/23/2018  Duration: 60 mins Overview Written procedures are to be established and followed for a time efficient and clear evidence of the quality related elements during the review and approval for release, including packaging and labeling, to determine compliance of the intermediates (FDA definition) and/or finished product with established specifications before a batch can be released for distribution BPRs, DHRs and laboratory control records for critical process steps are to be reviewed and