Ensuring compliance with healthcare laws is of utmost importance for healthcare providers
Compliance with the many laws, as well as
implementation of the necessary compliance initiatives are the means by which healthcare
providers and entities or organizations involved in any type of healthcare
transaction, especially those who bill or are involved with services payable by
a CMS program, play a part in the protection of the integrity of the CMS programs.
Developing and maintaining the necessary compliance
programs that place a special emphasis on auditing and monitoring, appropriate
training, receiving and responding to complaints and conducting investigations is
necessary for providers, entities and organizations that bill Medicare,
Medicaid or other government payor programs. Those whose compliance program
fails to incorporate the necessary control processes risk inviting potential
audits that could lead to civil, monetary and criminal penalties.
Understanding
risks is necessary for healthcare practices
The ways by which to understand potential
risks relating to their practice or organization and responding and mitigating
deficiencies are all-important for healthcare organizations if they have to
sustain their success and viability. This is also necessary if the organization
has to avoid or neutralize the impact of negative findings by an external audit
or investigative agency.
Moreover, with the many impactful changes
taking place in the healthcare delivery; healthcare provider reimbursement could
be affected. Quality of care and reduced costs will bring about changes into provider
reimbursement for services. Healthcare providers have to understand how these
changes are going to affect them.
Learning
ways of implementing compliant programs
A two-day in person seminar by
GlobalCompliancePanel, a highly reputable provider of professional trainings
for all areas of regulatory compliance, will offer understanding on all these
areas of healthcare compliance. This course, at which Gail Madison-Brown, a Registered
Nurse and attorney who has spent over 25 years in the healthcare industry, and
is Chief Clinical Trials Officer at UTHSCSA will be the Director, will focus on ways by which healthcare
organizations can devise means by which to stay compliant with the regulatory
guidelines and laws.
To enroll for this seminar and to get a
thorough understanding of how to implement practices that are compliant with
regulatory requirements, just visit
Ways
of building a robust and pragmatic compliance program
Attending this seminar will help
participants understand how to build a solid and practical compliance program.
Gail will introduce the basic healthcare compliance infrastructure necessary to
establish a comprehensive and proactive compliance program. She will then discuss
current government auditing agencies and audits that are underway, as well as
government agencies responsible for protecting the Medicare Trust Fund from fraud,
waste and abuse.
She will teach participants the ways of
identifying risks in their organizations, no matter what their size, by
conducting a risk assessment and developing a work plan based upon risk and
will help with the mitigation efforts. Apart from OCR audits and how to conduct
their own self-assessment in preparation for an audit, as well as ways of
addressing any identified deficiencies; participants will also learn how to
conduct auditing and monitoring activities and what to do with findings. Ways
of putting in place a complaint management system and conducting an
investigation will also be discussed. The Director will also offer user
friendly templates and tools, as well as numerous case scenarios to the
participants, which they can use to enhance current compliance programs.
Labels: biotech, Cleaning validation, fda, pharmaceutical, quality assurance, regulatory guidelines, Regulatory requirements
0 Comments:
Post a Comment
Subscribe to Post Comments [Atom]
<< Home