WEBINARS

 

Compliance Training Webinars for Regulated Industries

Click Search Icon to search relevant trainings by Keywords, Industry, Scheduled Month, Expert speaker name

3hr Virtual Seminar - Validation, Verification and Transfer of Analytical Methods – Implementing Guidelines from FDA/EMA, USP and ICH

webinar-speaker   Dr. Ludwig Huber

webinar-time   3 hrs

Product Id: 705753

This 3-Hr webinar on “Validation and Verification of Analytical Methods” by Dr. Huber will discuss the recent changes in guidance from regulatory agencies (FDA/EMA, USP and ICH) on method validation and transfer, integrated validation, verification and validation of analytical procedures for equivalency testing and statistical evaluation. He will teach how to execute document development, how to demonstrate FDA and EU compliance to auditors and inspectors, how to explain company’s strategy for method validation, verification, transfer and equivalency testing etc.

Recording Available

* Per Attendee $429

 

Residual Solvents: Take Advantage of the New Flexibility in Revised USP <467>

webinar-speaker   Gregory Martin

webinar-time   90 Min

Product Id: 705325

This webinar provides understanding of the requirements for residual solvents addressed in ICH, USP, EP and JP and focus on the recent changes to USP <467>. It will also help attendees utilize strategies to minimize the testing and resources required to meet the requirements.

Recording Available

* Per Attendee $249

 

Challenges with ASC Insurance Contracting vs. Out of Network Billing

webinar-speaker   Stephanie Thomas

webinar-time   60 Min

Product Id: 705676

This webinar will discover the top trends ASC facilities are facing with contracting with Medicare and third party payers. You will get the tips and tricks to ensure your negotiations are successful. You will learn to weigh the pros and cons of contracting to decide if out-of-network billing may be the best route for your business.

Recording Available

* Per Attendee $229

 

Three Key Risk Assessments in Your ERM Program - ERM, IT, and Internal Controls

webinar-speaker   Marci Malzahn

webinar-time   90 Min

Product Id: 705777

This risk assessment webinar will discuss how to do perform risk assessments for ERM, IT and Internal control function of your organization. Attendees will learn how to create/develop risk assessments, how to complete the ERM Risk Assessment using the ERM Risk Assessment Matrix. And how to complete the general IT Risk Assessment as well as a thorough Risk Assessment for your Internal Controls.

Recording Available

 

Stunning Changes in FDA's Software Regulation

webinar-speaker   Casper Uldriks

webinar-time   60 Min

Product Id: 705820

This webinar will highlight the changing circumstances with respect to software regulations and FDA’s approach from a regulation to voluntary standard. How to understand the qualifications and terms of participation to clear its software for marketing, what to do in case of cybersecurity intrusion and how to update regulatory program as mobile apps are removed from FDA’s regulatory oversight.

Recording Available

 

EU General Data Protection Regulation (GDPR): Compliance for Clinical Trials and Drug Development

webinar-speaker   Laura Brown

webinar-time   90 Min

Product Id: 705850

This webinar will discuss the new GDPR regulation requirements in the context of clinical trial data, how it applies to clinical trials and pharma industry, the personal data types including clinical trial data, what are the rights of clinical trials subjects, data access requests, informed consent, how to transfer clinical trial data outside EU, data breach reporting, penalties and how to put a data governance program and process to comply with GDPR regulations.

Recording Available

* Per Attendee $199

 

BREXIT – What's Changing for Life Science Product License Holders/Manufacturers and What You Need to Do Right Now?

webinar-speaker   Robert J Russell

webinar-time   90 Min

Product Id: 705811

This webinar will discuss how to accurately assess the impact of Brexit up on your operations and existing licensed life products in the UK and EU. How to plan to becoming compliant on “what is known” and how to be agile as the rest of implications become clearer. Impact on Filing Registrations with EMA in Q1 2019, How Will the UK’s Withdrawal Effect the Sunset Clause.

Recording Available

 

Safe Use of Ladders and Proper Climbing Practices; Fall Protection on Aerial Lifts; Proper Use of Staging

webinar-speaker   John J Meola

webinar-time   90 Min

Product Id: 705493

This webinar will review the best practices associated with use of ladders of all types, including the selection, inspection, storage and transport of ladders, along with safe practice when erecting, climbing, working from and descending a ladder. It will also discuss the process and practices related with aerial lifts and working from buckets on an extended boom.

Recording Available

* Per Attendee $179

 

Proposed NACHA Operating Rules - Hear the Latest NEWS in the Rules Space

webinar-speaker   Donna K Olheiser

webinar-time   60 Min

Product Id: 705835

This NACHA Operating Rules training session will provide the details on the proposed changes that potentially may be happening in the future. How it is going to impact you and what can you do about it.

Recording Available

 

How to Effectively Manage a Construction Project

webinar-speaker   Keith Warwick

webinar-time   90 Min

Product Id: 704858

This webinar training will explain the process to effectively manage construction projects. The Instructor will discuss reviews of plans and specification, inspection program, order of operations, identification of hazards and safety controls.

Recording Available

* Per Attendee $199

 

ICD-10-CM Official Guidelines for Coding and Reporting - FY 2019

webinar-speaker   Pamela Joslin

webinar-time   60 Min

Product Id: 705826

This webinar will discuss overviews of each of the four sections of 2019 ICD-10-CM Guidelines for Coding and Reporting. These are the guidelines that payers use when processing your claims. It will teach how accurate ICD-10 reporting ties to patient encounter, reimbursement and reporting, how to use chapter 7, how to use the A, D, S & documentation requirements. Expert will give examples of commonly used guidelines, such as sequencing, code first, code also, etiology and manifestation.

Recording Available

 

Medical Devices: Navigating FDA Requirements for Non-US Organizations

webinar-speaker   Jonathan Lee

webinar-time   90 Min

Product Id: 705823

This webinar will give an understanding of various processes and compliance requirements for US market entry by non-US medical device manufacturer. It will teach how to comply with pre-market requirements, how to get submission & product clearance/approval, what are various activities to be done post market entry of products (surveillance, reporting, audit, correction & removal).

Recording Available

 

Payment System Policy: FFIEC, Risk Management and Fraud Control

webinar-speaker   Ray Graber

webinar-time   90 Min

Product Id: 705810

This webinar is designed to provide understanding of payment system risk policy, how to do risk assessment and mitigate risk, what can be an optimal organizational structure to manage payment strategy.

Recording Available

 

How to Deal with Toxic Behaviours in Healthcare to Improve Patient Safety and Team Performance

webinar-speaker   Dr. Mitchell Kusy

webinar-time   60 Min

Product Id: 705840

In this Webinar you will learn how to find out toxic people those reduces patient safety, what is their modus operandi, and how to deal with them in terms of feedback, proactive and reactive strategies so that there is improvement of patient safety & team performance. How to spot such people and avoid hiring them.

Recording Available

 

FMLA Abuse: How to Identify, Investigate, Deny, and Terminate

webinar-speaker   Vanessa G Nelson

webinar-time   60 Min

Product Id: 703671

This webinar will assist employers with effective strategies to identify, investigate, and terminate FMLA abusers. Additionally, the course will also instruct employers on when it is appropriate to deny FMLA requests in accordance with the law.

Recording Available

* Per Attendee $199

 

How to Conduct an ASTM E 2018 Compliant Property Condition Assessment

webinar-speaker   Keith Warwick

webinar-time   60 Min

Product Id: 705369

Learn how to conduct a property condition assessment (PCA), schedule the field work, conduct the field work, and write the final report. The course will present techniques for developing cost estimates within a reasonable time frame. It will also discuss each of the components of ASTM E 2018 - 15 Standard Guide for Property Condition Assessments.

Recording Available

* Per Attendee $179

 

Transfer of Analytical Methods According to the USP Chapter <1224>

webinar-speaker   Dr. Ludwig Huber

webinar-time   75 Min

Product Id: 701971

This webinar will explain the final version of USP Chapter <1224> and FDA guidance for conducting and documenting method transfer between laboratories and sites, and provide tools for effective implementation.

Recording Available

* Per Attendee $179

 

Microsoft Excel: Using What-If Analysis-When, Why, and How

webinar-speaker   David H Ringstrom

webinar-time   90 Min

Product Id: 704929

This webinar will discuss the excel What-If Analysis tools within Microsoft Excel’s Data menu. In addition, it will explain Excel Scenario Manager, Data Table features, Excel’s Goal Seek feature, Excel Solver feature, FORECAST and more. Participants can avoid replicating worksheets. The advance functions can also help in comparing different scenario and extrapolate trends based on existing data in your spreadsheets.

Recording Available

* Per Attendee $129

 

How to Structure and Write a Job Hazard Analysis / Activity Hazard Analysis (JHA – AHA) in Accordance with OSHA 1926 – EM 385

webinar-speaker   John J Meola

webinar-time   90 Min

Product Id: 705500

This webinar will explore the common failures associated with organizing and writing Job Hazard Analysis / Activity Hazard Analysis (JHA – AHA) documents. It will also de-mystify some of the language and concepts in the traditional JHA process, namely the risk assessment calculator.

Recording Available

* Per Attendee $199

 

Trial Registration and Results Reporting on ClinicalTrials.gov

webinar-speaker   Marina Malikova

webinar-time   60 Min

Product Id: 705821

This session will explore the challenges clinical teams and sponsoring organization face in determining if a clinical trials is qualified and required to be registered, determining time frame for updates to be posted and reporting the results. It will explain HHS Final Rule and NIH Policy on Registration/Reporting in ClinicalTrials.gov and provide the steps to registration process in clinicaltrials.gov site.

Recording Available

* Per Attendee $199

 

 

 

BEST SELLERS

 

 

 

RECENTLY VIEWED

 

 

+1-888-717-2436

6201 America Center Drive Suite 240, San Jose, CA 95002, USA

Follow Us

facebook twitter linkedin youtube

 

Copyright © 2023 ComplianceOnline.com MetricStream
Our Policies: Terms of use | Privacy

PAYMENT METHOD: 100% Secure Transaction

payment method