Auditing Stress Testing and CCAR - How to Pass it?
Vidia Ramdeen
60 Min
Product Id: 705688
This session will discuss enterprise-wide stress testing program, the complexity of CCAR, A state of the art review of CCAR stress test design, CCAR frameworks, Organizing and validating the transmission chain from macro to market shocks down to single position shocks and how to balance art and science in stress test design.
World Class QA and Compliance Practices for Animal Health Manufacturing Companies
Jerry Chapman
60 Min
Product Id: 705628
This GMP training will elucidate the key elements of world class QA and compliance practices specifically for animal health manufacturing companies. These practices support a robust quality system, ensure the firm’s quality standards remain current, and inform the GMP auditing and training processes.
OSHA Voluntary Protection Program (VPP) Site Implementation Plan
Joe Keenan
120 Min
Product Id: 705179
The OSHA Voluntary Protection Program (VPP) is the highest award in Health and Safety Excellence that OSHA presents to an organization. This training program will guide attendees with best practices in implementing the OSHA VPP program. It will offer a broad overview of how to work with OSHA to achieve VPP site implementation success.
Health Reform Turbulence in the Trump Era: Market Impact and 2018 Outlook
Dennis Weissman
75 Min
Product Id: 705671
This health Reforms training will examine where U.S. health reform now stands in light of recent legislative and administrative changes, the outlook for additional policy initiatives in 2018 along with their market impact on payers and providers, and who will be the principal industry winners and losers in the ever changing health reform environment.
The Impact of Final ICH GCP E6 R2 Guideline on Budgeting and Contracts in Globalization Environment: Changes Affecting Sponsors, CROs, Clinical Investigators, Sites
Marina Malikova
60 Min
Product Id: 705649
In this revised ICH GCP guideline on budgeting and contracts for clinical trial webinar will discuss the impact of changes in ICH GCP E6 R2 on investigator, site, sponsors CROs roles and responsibilities and the impact of clinical trial conducts and organizational practices along with evaluate solutions/applicability/modifications of organizational SOPs, processes, procedures and staff training; and discuss opportunities for implementing the revised guideline.
FDA Communication Power Tools – Best Practices
Kwame Ulmer
60 Min
Product Id: 705667
This FDA communication best practices webinar will discuss the best practices for communication with FDA staff, general timing of communications, how to deal with deficiencies and key resources for premarket applications and post market communications.
3-Hr Virtual Training: Family Care and Medical Leave in California (CFRA/FMLA)
Jacquiline M Wagner
3 hrs
Product Id: 705665
This virtual seminar on Family Care and Medical Leave in California will examine the requirements for family care and medical leave, employers covered by the CFRA/FMLA, a covered employer’s duty to post notice of CFRA requirements and obligations, employees eligible for CFRA/FMLA leave, and more. The program will also explore the interplay between California’s Pregnancy Disability Leave law, CFRA/FMLA, compensation while on leave, continuation of benefits while on leave, employer’s prohibited actions under the CFRA, employee’s return to work policies, and more.
New York State Paid Family Leave: What You Need to Know Before 2018
Matthew W Burr
60 Min
Product Id: 705242
Understand the definition of New York State paid family leave and how it will impact your organization. The webinar will also discuss the process for filing, pending changes, and its association with the FMLA.
Medical Device Complaints Handling Strategies for Managing Your Biggest Compliance Challenge
Jeff Kasoff
60 Min
Product Id: 701788
This Medical device complaints handling webinar will discuss the best practices of complaint handling and how to include it in your CAPA program and how to apply risk management to the complaint handling system.
Batch Control and Inventory Management for Dietary Supplements
Chris Stefanadis
75 Min
Product Id: 705670
In this Dietary supplements batch control webinar learn what and how to create master manufacturing records, what batch production records to create and what to do with completed batch records as per FDA 21 CFR Part 111 requirements. Learn inventory management techniques that make the creation and management of Master and Batch production records easier.
Building a Vendor Qualification Program for FDA Regulated Industries
Jonathan M Lewis
60 Min
Product Id: 703467
This webinar will teach attendees best practices for building a sustainable vendor qualification program for FDA regulated industries. It will discuss common pitfalls to avoid when qualifying vendors.
Order Sets, Protocols, Preprinted & Standing Orders: CMS Interpretive Guidelines & Regulations
Sue Dill Calloway
120 Min
Product Id: 705631
This webinar will discuss the CMS requirements for standing orders and protocols in four separate sections. It will describe that all protocols must be approved by the Medical Staff even if the protocols are department specific.
PM Metrics and Alliance Management - Selecting and Managing Your CDMO
Christopher Verbicky
90 Min
Product Id: 705677
This project and alliance management webinar will present tools valuable for planning a project, identifying required outsourced activities, selecting a CDMO, monitoring/controlling an outsourced project, and communicating project performance to leadership.
High Impact Communications [B2B and B2C]: Writing Effective Emails, Letters, Memos, and Social Media Posts
Carly Souther
60 Min
Product Id: 705661
In this communication best practice webinar you will learn how to write high impact emails, letters, memos and social media posts which conveys the content and context in the best way to have high impact on target audience. Learn how to formulate message, correspondence based on relationships, tone in written form. Understand major email mistakes and write purposeful and reader-focused emails.
NAFTA: Disruption Implications - How to Avoid Consequences
Raymond Sullivan
60 Min
Product Id: 705686
This trade compliance webinar will discuss the impact and how you can be ready from the eventualities which can come out of recent updates and negotiations related to trade and NAFTA agreements which is going to happen in coming days
Introduction to MS Power BI for Dashboards
Tom Fragale
100 Min
Product Id: 705605
If you understand Excel charts and Pivot Tables then you can leverage your existing knowledge and skills to create powerful, interactive dashboards and analyses unthinkable until recently. This 100-minute webinar takes you from Excel Dashboards to easier and more powerful MS Power BI dashboards. With this training you’ll learn the basics of implementing "do it yourself business intelligence" using Power BI.
Transgender Employees in the Workplace
Kristin Robinson
60 Min
Product Id: 705465
Learn how best to manage workplace issues surrounding an employee's gender transition.
The Compliance Officer's Toolkit: Best Practices for Compensating and Contracting With Physicians
Joseph Wolfe
60 Min
Product Id: 705435
This webinar will provide an overview of the technical requirements of the health care laws such as Stark Law, Anti-Kickback Statute, Civil Monetary Penalties Law, False Claims Act, etc. It will also discuss best practices that health care organizations can follow to avoid compliance traps related to these laws.
Forecasting with Excel's Powerful Sensitivity Tools - Scroll Bars, Goal Seek, Data Tables, Solver and Scenario Manager
Miles Hutchinson
90 Min
Product Id: 703156
In this financial forecasting webinar learn how to use Excel’s powerful sensitivity tools and design efficient forecasting models. Application of scroll bars, goal seek, data tables, solver and scenario manager. Also received bonus material containing the demo model, complete with instructions for each of these tools!
Change Control Best Practices: Avoiding Unintended Consequences of Changes
Andrew Campbell
90 Min
Product Id: 703540
This webinar will provide an overview of regulatory requirements for change control. It will focus on changes to equipment, facilities, materials/components, test methods, suppliers, specifications, etc.