Skip to main content

3-Hour Virtual Seminar on HIPAA Compliance Certification

Angela Bazigos, is the CEO of Touchstone Technologies, Inc. She has 40 years of experience working in hospitals and Pharma industry. Her background includes companies like Roche, Novartis, Genentech and PriceWaterhouseCoopers in GLP, GCP, GMP, Medical Device and Data Integrity Roles. She has held positions such as Chief Compliance Officer, QA Director and has acted on behalf CEO for communications with FDA. 


Webinar Id: HIPAB001
Time: 10:00 AM PST | 01:00 PM EST
Date: 09/29/2017
Duration 180 mins 

Overview
HIPAA, which stands for Health Insurance Portability & Accountability Act, does not just apply to health insurance. The rules apply to all companies with Personal Health Information (PHI) in electronic formats -doctors, health plans, pharma organizations, government programs, research organizations, testing organizations, pharmacies, clinics, IT services for regulated organizations, and more. In March of 2013, the HIPAA Omnibus Final Rule took effect, with major changes around Business Associate definitions, requirements for security breaches, and increased focus on privacy and greater fines for non-compliance.
Why should you attend this webinar?
Anyone dealing with Patient Health Information (PHI) in the Pharma / Biotech / Medical Device and other Lifesciences & healthcare companies, is subject to the HIPAA regulations
This webinar will explain HIPAA and the impact of HIPAA to the Lifesciences & healthcare Industries.
This course will give you all the tools that you need to be certified as HIPAA Security Training Certification
Areas Covered in the Session:
  1. HIPAA Privacy Rule
    • Do not allow any impermissible uses or disclosures of PHI.
    • Provide breach notification to the Covered Entity.
    • Provide either the individual or the Covered Entity access to PHI.
    • Disclose PHI to the Secretary of HHS, if compelled to do so.
    • Provide an accounting of disclosures.
    • Comply with the requirements of the HIPAA Security Rule.
  2. HIPAA Security Rule
    • Technical Safeguards
      • Access Control
      • Audit Controls
      • Integrity
      • Authentication
      • Transmission Security
    • Physical Safeguards
      • Facility Access Controls
      • Workstation Use
      • Workstation Security
      • Device and Media Controls
    • Administrative Safeguards
      • Security Management Process
      • Assigned Security Responsibility
      • Workforce Security
      • Information Access Management
      • Security Awareness and Training
      • Security Incident Procedures
      • Contingency Plan
      • Evaluation
      • Business Associate Contracts and Other Arrangements
  3. HIPAA Enforcement Rule
    • Penalty for a HIPAA violation
    • HHS Enforcement Rule
  4. HIPAA Breach Notification Rule
    • HHS Breach Notification Rule
  5. HIPAA Knowledge Quiz
Who can Benefit:
  • All Health Care Personnel, including 
    • emergency care providers, 
    • laboratory personnel, 
    • autopsy personnel, 
    • hospital employees, 
    • interns and 
    • medical students, 
    • nursing staff and students, 
    • physicians, 
    • surgeons 
    • dentists, 
    • labor and delivery room personnel, 
    • laboratory technicians, 
    • health facility sanitary staff
    • clinical waste handlers and 
    • health care professionals at all levels Who are at risk
    • Hospitals & Healthcare Personnel
  • Pharma, Biotech, Medical Device Personnel dealing with patients Regulatory personnel e.g. FDA, HHS, OSHA etc.
    • Clinical Research Associates
    • Clinical Auditors
    • Clinical Operations managers
    • VP of IT
    • IT Managers
    • IT Personnel
    • Quality Control
    • Quality Assurance
    • Regulatory Affairs
    • Document control managers


Compliance Key INC
717-208-8666

Comments

Popular posts from this blog

Essentials of Affirmative Action and OFCCP Compliance

Compliance Key INC  -  Human Resource Training Online                                                                  Janette Levey Frisch Janette Levey Frisch is Keynote Speaker at Compliance key Inc. She is founder of  The EmpLAWyerologist Firm, has over 20 years of legal experience, more than 10 of which she has spent in Employment Law. It was during her tenure as sole in-house counsel for a mid-size staffing company headquartered in Central New Jersey, with operations all over the continental US, that she truly developed her passion for Employment Law.   Webinar Id:   CICJE001  10.00 AM PT | 01.00 PM ET   01/09/2018  Duration: 90 mins  Overview If you are a federal contractor, having a firm grasp on the essentials ...

Risk and Controls Matrix for SOX, Assurance and Internal Audit

Compliance Key INC  -  SOX Training Online Overview This webinar is created to equip young risk and compliance professionals with the skills necessary to prepare a Risk and Controls Matrix, including the following: Discover the objectives, components and requirements of effective internal controls Leveraging internal control frameworks to create a risk and controls matrix Developing risk identification and management strategies to implement now Learning how to design internal controls Learning how to evaluate the design and operating effectiveness of internal controls Why should you attend this webinar? Whether you are planning a SOX engagement, or an internal audit, regulatory compliance requirements, or other separate evaluations, just where do you start with planning for the engagement? How do you complete the necessary risk and control documentation that you will need to successfully complete the engagement? Attend this webinar to learn more. Areas...

Understanding Design Controls

Compliance Key INC  -  Medical Device Training Overview Design Controls are the processes used to design, develop, and manage medical devices that you manufacture. They are mandated by federal regulation, however, the regulations concerning design controls are vague in terms of the specific process steps required and the approaches that should be taken to achieve compliance should be developed. Knowing how the FDA both views and examines design controls is crucial to achieving compliance throughout the life of the medical devices you manufacture and is one of the most valuable compliance subject areas to explore. Noncompliance in design controls, which are consistently uncovered by the FDA during inspections and examinations, are concerned with the design control process that has been designed and applied and the documentation required to support each design control step. The specific sections of the regulations that apply to design controls include CFR 21 Part 820 Qua...