Skip to main content

How to Prepare a HIPAA Compliant Disaster Recovery Plan

Overview
This webinar focuses on an area often missed in performing HIPAA assessments: the business continuation and disaster recovery planning. This session takes the participants through the process of considering what can/may happen that could put the healthcare organization out of business and how to develop methods for mitigating those risks.
Why should you attend this webinar?
HIPAA has clear requirements regarding how a healthcare organization needs to respond to a potentially catastrophic event to enable the organization to maintain its ability to provide health care services and to protect their patient's health care information from being disclosed to an unauthorized individual. This webinar provides the basics of how the healthcare organization can meet this HIPAA requirement.
Areas Covered in the Session:
  • Why a disaster recovery plan is needed to be HIPAA compliant 
  • What are the components of an effective disaster recovery plan
  • How to define mission critical processes and information and how to cover these areas in a disaster recovery plan
  • What is the role of your IT department in preparing for and implementing a disaster recovery plan
  • How to develop an effective disaster recovery plan
Who can Benefit:
Anyone involved in providing health care services, either directly or indirectly. This includes health care organization ownership and senior management, office management, business associates, physicians, ancillary services organizations (pharmacies, labs, radiology). Healthcare IT should also attend to understand their role in helping the healthcare organization in becoming HIPAA compliant.


Comments

Popular posts from this blog

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...

Conducting a Software Validation of Medical Device to Meet FDA Requirements

Compliance Key INC -  Medical Device Training                                           Edwin Waldbusser Ed is Keynote Speaker at Compliance key Inc . He is retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. Products included IVD devices, kidney dialysis systems and inhalation devices. QS experience includes design control, risk analysis, CAPA, software validation, supplier qualification/ control and manufacturing.   Webinar Id:  LSHCMEW007  10.00 AM PT | 01.00 PM ET  12/04/2017   Duration 90 mins  Overview This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product. Software validation is much more than testing.We will explain the role of risk analysi...

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 ...