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Conferences in California, United States
How Does Compliance with 21 CFR Part 11 Help Ensure Data Integrity and Subject Safety in Clinical Research - Webinar By MentorHealth
Overview: Electronic medical records and electronic handling of study data is increasingly common. To involve computer systems in clinical research implies knowledge of 21 CFR Part 11(ELECTRONIC RECORDS; ELECTRONIC SIGNATURES) and all of the ramifications of this Part of the code is essential.
How to Deal With the Disruptive Practitioner - Webinar By MentorHealth
Overview: This webinar will discuss the development of such a policy, including a statement in the medical staff bylaws to the effect that each member of the staff is expected to comply with all of the hospital and medical staff rules, regulations, policies and procedures relating to behavior and performance.
Webinar on Patient Centered Care - Webinar By MentorHealth
Colorado Foundation for Medical Care (CFMC) hosts an online activity evaluation system, certificate and outcomes measurement process. Following the activity, you must link to CFMC’s online site (link below) to complete the evaluation form in order to receive your certificate of credit. Once the evaluation form is complete and submitted, you will be automatically sent a copy of your certificate via email. Please note, participants must attend the entire activity to receive all types of credit.
3-Hour Virtual Seminar On OSHA Injury and Illness Recordkeeping Analysis - Webinar By MentorHealth
Overview: This webinar will provide a description of what the requirements for OSHA Injury and Illness reporting, as well as what constitutes the various acceptable categories for reportable and no reportable injuries. The webinar will also define common terms used by OSHA and the methods for calculating the injury and illness rates in your facility.
The Art of the Audit - Webinar By MentorHealth
Overview: This one webinar could save your practice thousands of dollars recouped from denied claims. Get dozens of ideas and tips for bringing back reimbursement rightfully due. This in-depth session will provide an action plan with examples on how to win carrier appeals every time.
The Clinical Genome Conference
Bio-IT World and Cambridge Healthtech Institute are again proud to host The 2nd Annual TCGC: The Clinical Genome Conference, inviting stakeholders from all arenas impacting clinical genomics to share new findings and solutions for advancing the application of clinical genome sequencing.
TCGC brings together many constituencies for frank and vital discussion of the applications, questions and solutions surrounding clinical genome analysis, including scientists, physicians, diagnosticians, genetic counselors, bioinformaticists, ethicists, regulators, insurers, lawyers, and administrators. This 2-part event covers the science of sequencing and the business of translating genomics into the clinic.
Return to Work - How and Why it is a Win-Wins - Webinar By MentorHealth
Overview: Learn the financial and legal implications of returning an employee with a work injury to the job the very next day after a work injury.Also learn the risks and liabilities for failing to do so. Practical step by step processes to implement a return to work program with be covered, forms to use, how to assign responsibilities, and likely problems you will encounter.
How to Create, Manage and Implement a Coding Compliance Plan - Webinar By MentorHealth
Overview: This session will provide a strategy and detailed examples how to create and implement a coding compliance plan. A plan is not a static document; it is working document that must be reviewed and implementing constantly and continually. Jeff will use his 15 plus years as an auditor, a coding training and documentation specialist to help you create a compliance plan that works for your practice.
The GCP-ICH Obligations of Sponsors, Monitors, and Investigators - Barriers and Solutions - Webinar By MentorHealth
Overview: There is an increasing frequency of real-time FDA Audits of trials and it seems that no one is well prepared. It is the obligation of the major players in the drug development process (the Investigator and the study Sponsor) to be sure studies are carried out correctly so that errors and mistakes are found and corrected by them (CAPA) and not by an FDA Investigator.
HIPAA-HITECH assessment for Healthcare Business Associates - Webinar By MentorHealth
Overview: As the compliance deadline for new HIPAA/HITECH rule approaches, it becomes imperative for healthcare business associate organizations to develop strategies to protect electronic health information, and comply with HIPAA/HITECH regulations.
