Nearly everyone worries, over 25% of people believe they worry too much, and about 6% of people will suffer from generalized anxiety disorder (GAD).
GAD is particularly important to treat as frequently leads to depression, medical problems, and more distressing anxiety disorders like panic disorder and OCD.
In this webinar we will discuss the most recent CPT changes as well as review past CPT updates to commonly performed pain management services, Also we will discuss HCPCS codes and how to best find the medication we are looking for.
This session will focus on the rights of individuals to communicate in the manner they desire, and how a medical office can decide what is an acceptable process for communications with individuals.
In this webinar you will learn how perspective taking is a fundamental concern when treating Asperger Syndrome/High Functioning Autism, At the completion of this presentation, you will be able to view your clients diagnosed with Asperger syndrome/High Functioning Autism in a different manner, You will be able to develop strategies to help them achieve success, not only in your office, but also in any social setting.
This webinar will focus on the Stark Law's underlying technical requirements and key tenets of defensibility as they apply to physician practice acquisitions, also will discuss best practices for drafting physician employment agreements, related compensation plans and facilitating effective onboarding
This HIPAA Cyber Crime Training will discuss how to use the HIPAA rules to prevent, prepare, respond and recover from Cyber Attack , Ransomware is the easiest and safest way for cyber-criminals to extort money from the Healthcare Industry.
This session will explore the complications and requirements of each of the rules controlling student health information, HIPAA, FERPA, and 42 CFR Part 2, and provide insights into how to apply the rules in an education setting.
Recent cases and/or enforcement actions involving the Federal Civil False Claims Act (FCA) as well as the Medicare-Medicaid Anti-Kickback Statute (AKS) and/or Federal Physician Self Referral Law (Stark II) raise serious concerns regarding compliance issues with the hospital, physician practices, and other healthcare entities.
This webinar will begin with a general discussion of technical writing and its role within the life sciences. Technical writers produce a variety of technical documents that are required to manage and direct regulated operations and to meet regulatory requirements. We will spend some time in this webinar discussing those document types, their importance, and the consequences of the messages are unclear or misunderstood.
After setting the stage for this content, we delve into the writing process beginning with the audience and how the audience must be analyzed to determine the level of writing that must be employed to complete the document.
This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018 and December of 2017 respectively, and also cover multiple scenarios and FAQ’s relating to Substance Abuse Records, Mental Health Records, Alcohol Abuse Records, and the proper ways to secure this information and/or release this information.
An overview of a comparative analysis will be presented comparing SAMHSA to the HIPAA laws relating to protected health information in general.
This 6-hour webinar takes the participants through HIPAA compliance from start to compliance.
The first presentation explains the history of HIPAA, why it came into being and its evolution. This covers what HIPAA is, what steps have to be performed to be HIPAA compliant and what HIPAA compliance is. It also provides definitions to key HIPAA terms, how to define a Business Associate and how to contract with Business Associates.
The second part of the first presentation is an overview of how to manage the HIPAA compliance project.
When new drugs or devices are tested in humans, the data generated by, and related to, these trials are known as clinical data. This data represents a huge investment by the biopharmaceutical or device company and is one of its greatest assets. It is this data that will eventually make a new product both useful as a treatment or therapy and marketable.
The management of clinical data, from its collection during a trial to its extraction for analysis, has become a critical element in the steps to prepare a regulatory submission and to obtain approval to market a treatment. As its importance has grown, clinical data management (CDM) has changed from an essentially clerical task in the late 1970s and early 1980s to the highly computerized specialty it is today.
Attend this 90 minutes presentation to gain a fundamental understanding of
FDA's regulation of Dietary Supplements, Dietary supplements are regulated products, also Dietary supplement marketing, manufacturing, labeling, and advertising are all covered by regulations enforced by FDA.
Why should you Attend:
There is confusion in the industry as just what type of manufacturing
controls and record keeping, and labeling content is required by the FDA,
and this confusion continues to cause regulatory problems for many new
and established companies in this industry.
Over application or incorrect usage of lubricants can lead to insanitary
conditions or contamination. Often condensate plays a big part in
refrigerated foods and mixed with improper use of lubricants can spell
potential problems in the environment.
Why should you Attend:
FDA at one time approved and updated a lubricant listing for the food
industry. This is now the responsibility of manufactures to manage.
In this webinar speaker will explain how to choose the tests to be conducted
and the studies that must be completed prior to the actual validation test.
Why should you Attend:
We will explain how to choose the tests to be conducted and the studies
that must be completed prior to the actual validation test. The post test
participant inquiry is critical to validation success. we will describe how to do this.