90-minute webinar on "Current Trends in Clinical Research Compliance" from Compliance4All on July 10
The processes and approaches that increase fiscal return and mitigate fiscal compliance risk for clinical trials is of critical importance if companies have to make research profitable.
- Chicago, IL (1888PressRelease) July 03, 2018 - Compliance4All, a leading provider of professional trainings for all the areas of regulatory compliance, will organize a webinar on July 10 on the topic, “Current Trends in Clinical Research Compliance”. Marina Malikova, who is Executive Director, Surgical Translational Research: Operations and Compliance, will be the expert at this webinar. Please visit http://bit.ly/2KDn3wy to enroll for this webinar and gain understanding of current best practices in the vital areas of clinical research.
Clinical research compliance is a must for facing current challenges and opportunities in clinical research. Meeting the guidelines set out for clinical research is important if the company carrying out clinical research is to pass its clinical research activities successfully. While understanding and implementing best practices for research and compliance practices for clinical research is important; a clear and thorough understanding of the processes and approaches that increase fiscal return and mitigate fiscal compliance risk for clinical trials is of critical importance if companies have to make research profitable.
This webinar is designed to help companies gain perspectives on the ability to develop robust budgets and to ensure billing compliance and adherence to CMS-Medicare regulations for clinical trials, which many clinical sites, sponsors and Contract Research Organizations (CROs) find quite challenging. Dr. Malikova, who has extensive experience in clinical trials and basic biomedical research operations, quality assurance, risk management, safety monitoring, strategic planning, and macro-management of research programs; will explain the current best practices for all the core areas of clinical research, including administration, billing compliance, development of policies, and procedures and training in accordance with current regulations.
Reducing the risks of fiscal audits
The risks of fiscal audit get increased when clinical trial companies lack fiscal forecasting and carry on unspecified billing compliance practices. A risk-based approach that includes not only a strategy but tools to define key indicators to measure specific risks needs to be adapted. While teaching the participants of this webinar the ways of doing this; Dr. Malikova will help them understand what strategies they need to implement for covering true costs related to clinical research, which distinguishes them from routine care charges. She will also offer methodologies to avoid false claims and/or wrongful billing.
She will cover the following areas at this webinar:
- Research Billing
- Medicare Coverage Analysis
- Human Subject Protection
- Conflict of Interest
- Best Practices for Research Administration
- Grant Management and Compliance
- Research Misconduct
- Implementation of Good Clinical Practices
- Policies, Procedure Development and Training.
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