WEBINARS

 

Risk-Based Monitoring Beyond the RACT

webinar-speaker   Beat Widler

webinar-time   60 Min

Product Id: 704721

This training program will explain what the strengths and weaknesses of the RACT are and where it should be used with caution. It will also elaborate on what needs to be done to establish a comprehensive risk management approach to support risk-based quality management in clinical trials.

Recording Available

 

Designing Effective Controls, Security Safeguards and Governance by a Risk-Based Methodology

webinar-speaker   Javier Kuong

webinar-time   120 Min

Product Id: 704656

This training program will provide a practical and structured methodology for the design of governance, controls and security provisions. The methodology can be applied to participants’ real work environment immediately. Participants will also benefit from comparing their present governance and controls design practices with the structured, risk-based methodology presented in the webinar.

Recording Available

 

FMLA, ADA & Workers Comp - Crafting Policies and Procedures for Managing Employee Leave

webinar-speaker   Janette Levey Frisch

webinar-time   90 Min

Product Id: 704425

This webinar will decrypt the complexity of FMLA, ADA, workers comp & state employee leave laws. Participants will learn the critical components, difference and laws governing them in order to craft effective leave policies and manage leave abuse.

Recording Available

* Per Attendee $149

 

Patient Access of Records under HIPAA - New HHS Guidance, New Focus for HIPAA Audits

webinar-speaker   Jim Sheldon-Dean

webinar-time   90 Min

Product Id: 704757

This training program will help health information professionals understand what they have to do, and when, and what to keep in mind as they move forward, in order to be in compliance with the new HHS guidance. It will provide a comprehensive look at the guidance and the changes in the HIPAA rules on access and prepare attendees for the process of incorporating the guidance and the changes in how they do business in their facilities.

Recording Available

* Per Attendee $179

 

Navigating Standard 1.2.7 - The Regulation of Nutrition and Health Claims in Australia/NZ

webinar-speaker   Janine Curll

webinar-time   90 Min

Product Id: 704692

This training program will discuss what is a NCC (Nutrition Content Claims), a GLHC (General Level Health Claims), a HLHC (High Level Health Claims), and the conditions for making these claims. Attendees will understand the conditions on the types of foods that can carry nutrition content and health claims and the process to self–substantiate a food health relationship and requirements for FSANZ notification.

Recording Available

* Per Attendee $199

 

ISO 14001:2015 - Understanding Documenting and Auditing - Module 3

webinar-speaker   Michael Aust

webinar-time   60 Min

Product Id: 704748

This final training program in the series will help identify how the environment impacts your organization under the new ISO 14001:2015 standard. It will detail how to properly develop an audit schedule and plan for internal and external audits. The session will also describe the next steps to get compliant with the new standard, while preparing for audit and proper documentation.

Recording Available

 

ICD-10 Other Factors Affecting Revenue

webinar-speaker   Dorothy Steed

webinar-time   60 Min

Product Id: 704746

If you are experiencing claims problems, reduced revenue, increased requests for medical records, or receiving payer push back about you’re coding and billing quality, this training program is for you. All these areas will be discussed in the webinar.

Recording Available

 

FDA's Medical Device Software Regulation

webinar-speaker   Casper Uldriks

webinar-time   90 Min

Product Id: 704749

This training program will focus on FDA software guidance. It will elaborate on applying current provisions that NIST (National Institute of Science and Technology) has put forth in recent reports that FDA will integrate into its regulatory oversight as well.

Recording Available

* Per Attendee $169

 

When Studies are Exempted from IND Requirements: Understanding the Criteria and the Consequences

webinar-speaker   Jennifer Holcomb

webinar-time   60 Min

Product Id: 702345

This Clinical compliance training will review the purpose of INDs and the process for obtaining an IND. Attendees will gain a complete understanding of the criteria for exemption and the impact an exemption has on a study.

Recording Available

* Per Attendee $229

 

3-Hr Virtual Training: What to Expect in a Federal HIPAA Audit and How to Avoid an Audit Altogether

webinar-speaker   Brian Tuttle

webinar-time   3 hrs

Product Id: 704761

This webinar training will discuss changes with the Health and Human Services in regards to the enforcement of the HIPAA laws already on the books and new risks specific to business associates. It will also discuss factors that might cause an unwanted visit or letter from the Office of Civil Rights and how to prepare for the audit and deal with federal and state laws.

Recording Available

 

3-hr Virtual Seminar - Trade with Southern Hemisphere: DR-CAFTA (Dominican Republic-Central America)

webinar-speaker   Linda B Sarabia

webinar-time   3 hrs

Product Id: 704715

This training program on CAFTA import and export will detail the US requirements to export and import procedures to CAFTA Nations. It will also discuss commercial and customs document requirements, tariffs and applicable duties, countervailing and antidumping duties, and highlight the difference and interaction between CAFTA and NAFTA.

Recording Available

 

Social Networks and Pharmacovigilance: What Will Change?

webinar-speaker   Marco Anelli

webinar-time   90 Min

Product Id: 704690

This training program will examine the different types of social networks (Facebook, Twitter, etc.) and help identify similarities, differences, and challenges for pharmacovigilance (PV) professionals. It will also analyze social networks and the new approach to benefit/risk ratio.

Recording Available

 

Structuring and Implementing Hospital-Physician Medical Director and Administrative Arrangements: Key Legal Considerations for Health Systems, Hospitals and Medical Groups - Part I

webinar-speaker   Joseph Wolfe

webinar-time   60 Min

Product Id: 704742

Given the substantial awards and settlements in recent enforcement actions, Stark Law compliance has become more than just a compliance issue: it is an enterprise risk management issue. As medical groups, hospitals, and health systems transition to more innovative compensation structures, this training program will focus on managing compliance and enterprise risk by ensuring their medical director and administrative arrangements are defensible under the Stark Law.

Recording Available

* Per Attendee $179

 

Dos & Don'ts Related to Information Security and Data Privacy

webinar-speaker   Marc Perl

webinar-time   60 Min

Product Id: 704736

This training program will prepare your organization to understand the need for data security, the steps that can be taken to institute or augment your data security policies/procedures, and the implementation of the needed controls. This webinar will introduce attendees to a set of known and respected data security standards that can be employed by your organization to improve your security. Attendees will walk away with ideas to leverage the curriculum with their existing security infrastructure.

Recording Available

* Per Attendee $249

 

Sterilizing Grade and Prefilter

webinar-speaker   Mark Trotter

webinar-time   90 Min

Product Id: 704703

This training program will review the latest industry filtration technologies and standards with an overview of regulatory requirements. It will also discuss why and how to determine which filter, the media, and pore ratings that are appropriate for various filtration applications. The program is designed for experienced as well as those new to biopharmaceutical processes. The need-to-know current requirements for specifying sterilizing grade and prefilters in biopharm processes will also be discussed.

Recording Available

 

FDA Pre-Approval Inspection Readiness: Actionable Steps to Prepare for a BIMO Inspection

webinar-speaker   Nicole Tesar

webinar-time   60 Min

Product Id: 704640

This 60-minute training program is designed for those working in the field of clinical research either as a sponsor (pharmaceutical/biotech company) or a research site. The session will discuss key FDA inspection terminology, types of BIMO inspections, site inspection procedures, and sponsor inspection procedures. Attendees will understand when an inspection is likely to be scheduled and the current trends in findings.

Recording Available

 

Hazwoper Training: Tips to Hazardous Waste Cleanup per OSHA’s Guidance

webinar-speaker   Sheldon Primus

webinar-time   60 Min

Product Id: 704602

This training program will focus on helping attendees identify the hazards of chemical spill cleanup, understand the steps to properly clean up hazardous chemical spills, and gain a basic knowledge of the Resource Conservation and Recovery Act and Process Safety Management.

Recording Available

 

How to Write Error Free and FDA Compliant Procedures

webinar-speaker   Ginette M Collazo

webinar-time   90 Min

Product Id: 704122

This training program will focus on the importance of procedures. Attendees will learn why people avoid procedures and understand common human errors and deviations related to the use of procedures.

Recording Available

* Per Attendee $179

 

ISO 14001:2015 - Advanced Overview - Module 2

webinar-speaker   Michael Aust

webinar-time   60 Min

Product Id: 704728

ISO 14001 is the world's best-known environmental management system standard, and it provides a systematic framework to help organizations protect the environment through balanced socio-economic means. This training program in the two-part series will offer an advanced overview of ISO 14001:2015 and what the updates mean for your business.

Recording Available

 

How to Bill Medicare for Durable Medical Equipment and Stay Legally Compliant

webinar-speaker   Gregory J Simms

webinar-time   60 Min

Product Id: 702134

This training program will expound on how treating your Medicare patients with durable medical equipment (DME) can be great for patient clinical outcomes, a great revenue stream, and can be legally compliant. It will also lower healthcare costs. However, one must know how to get the proper licensure and know the federal and state guidelines.

Recording Available

* Per Attendee $50

 

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