Skip to main content

Regulatory Compliance and Culture Change

      Compliance Key INC - Medical Device Training


                                          Carmen Bowman
Carmen Bowman is Keynote Speaker at Compliance key Inc. she is a consultant, trainer, author and owner of Edu-Catering: Catering Education for Compliance and Culture Change turning her former role of regulator into educator. Carmen was a Colorado state surveyor for nine years, a policy analyst with CMS Central Office where she taught the national Basic Surveyor Course and the first certified activity professional to be a surveyor.
 Webinar Id: LSHCCCB003
 12:30 PM PT | 03:30 PM ET
 11/15/2017
 Duration 90 mins 
Overview
CMS regulations have always supported the principles and practices of culture change and now even more so. See how the new CMS regulations support culture change practices and how the national culture change movement affected the new requirements .Learn how a transformed culture centered around resident autonomy and regard, naturally meets regulations. It is our time to now only link culture change to the new CMS requirements but leverage our proven person-centered care and culture change practices to be more compliant with regulations than ever before.
Why should you attend this webinar?
Many think that culture changes cannot take place, but regulations have always supported these practices and do now even more so.
Areas Covered in the Session:
  • New CMS Regulations
  • Common culture change practices
  • How culture change practices meet and exceed regulations
Who can Benefit:
Anyone who works in a nursing home.
Compliance Key INC

Comments

Popular posts from this blog

The 5 most Dangerous Risks Under New HIPAA Laws

Compliance Key  -   Online hipaa training for employees in US Overview This 90-minute webinar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2018. We will go into detail about the 5 biggest "gotcha's" related to compliance with this enigmatic law. I will also speak of multiple litigated cases I have been involved with involving HIPAA compliance (or lack there of areas also covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT.  The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, there is so much misleading information regarding the do's and don'ts with HIPAA - I want to add clarity for compliance officers and what you guys need to do and how to best im...

Strategies for Becoming a Business Partner to Your Healthcare Leaders.Compliance Key INC -

Compliance Key INC  -  Healthcare Training Online                                                    Jay Anstine 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. In tackling the countless regulatory and operational issues for these diverse organization types, he has developed a deep understanding of the business of healthcare and the regulations that govern the industry.  Webinar Id:  LSHCSJA022  10:00 AM PT | 01:00 PM ET  12/13/2017  Duration 60 mins  Overview All too often compliance is seen as an obstacle or otherwise viewed negatively by healthcare leaders. This presentation will discuss strategies and insights to help the compliance of...

CMO Supplier Quality Agreements :- How to Comply with new FDA and EU Guidelines for Contract Drug Manufacturer

Compliance Key INC  -  Compliance Online Training                                             Roger Cowan Roger Cowan is the Keynote Spaker at Compliance Key Inc. He is the founder and owner of R Cowan Consulting Services LLC, a consulting company specializing primarily in the area of pharmaceutical contract manufacturing. He has 35 years experience in pharmaceutical quality assurance and manufacturing.  Webinar Id:  LSHCRC007  10:00 AM PT | 01:00 PM ET  12/07/2017  Duration 60 mins Overview A Quality Agreement is a contract between a pharmaceutical firm and a GMP Contract Manufacturer detailing the responsibilities of each party in assuring the quality, safety, and efficacy of the manufactured drug.  Recently, the EU and the FDA issued regulatory guidance to bring some clarity and consistenc...