Utilization of a Lifecycle Validation Approach via a Quality System to Reduce Costs and Increase Compliance
James Carron
90 Min
Product Id: 703412
This webinar will explain how to incorporate a quality system into the validation process to reduce cost and ensure compliance. It will cover the analysis, design and initiation phases, including full implementation of the incorporation.
How to Develop a Successful Business Continuity Audit Program that Will Help Ensure Your Program is Compliant and Effective
Michael C Redmond
60 Min
Product Id: 703592
Get trained on developing an effective business continuity audit process that ensures an organization’s ability to remain in business in a disaster. Learn how to audit a business continuity plan and ensure it has all the components.
Qualification Sample Size and Statistical Confidence for Pharma Process Performance Qualification (PPQ)
Marvin Iglehart
90 Min
Product Id: 703579
This webinar will discuss the requirements and general expectations for Stage 2 – Process Qualification, the key concepts that lead to the basis of confidence level and/or statistical confidence and how to apply the concepts in practical use for validation, including acceptance criterion.
Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks
Dr. Joni E Johnston
90 Min
Product Id: 701777
In this progressive discipline and employee termination webinar understand the best practices of creating performance improvement plans, and how to avoid mistakes while disciplining or terminating employees (including older and protected class workers).
Internal Auditors: Preparing to Conduct Effective Audits
Richard Cascarino
90 Min
Product Id: 703595
This webinar will help attendees identify the key tasks to be performed as internal auditors in the course of an audit and develop appropriate metrics to measure progress.
Updated EU filing and registration procedures (including the new variation rules coming in to force)
Robert J Russell
60 Min
Product Id: 701535
This EU filing and Registration webinar will discuss in brief all the new EU clinical directives, its Impact and how companies can effectively align their filing and registrations processes to effectively implement the requirements of the regulations.
Cleaning Validation Swab Recovery Studies and Analysis
Keith Bader
60 Min
Product Id: 701400
This webinar provides a thorough demonstration of what information can be extracted from a surface swab recovery study for maximum leverage in a cleaning and cleaning validation program.
How to conduct Risk Assessments as per ISO 31000/31010(SOX)
Kenneth Barden
90 Min
Product Id: 701744
This Risk Assessment training will focus on the criteria established for ISO Standards 31000 and 31010. It will look at how a company can identify and manage its risks, and how effective risk management techniques can translate into better marketing and profitable opportunities for a business enterprise.
The JOBS Act - the Regulation D Offering Reborn
Warren R Markowitz
60 Min
Product Id: 703589
This webinar will focus on the comparison between the old and new Reg D Rule 506 Offering and will highlight the importance of compliance in this new arena. It will also discuss the roles and responsibilities of counsel and company management.
OSHA's Personal Protective Equipment (PPE) Standard, 29 CFR 1910.132
Randall Charpentier
90 Min
Product Id: 703587
This webinar will discuss in detail the requirements of personal protective equipment (PPE) and its use. Attendees will learn best practices to ensure compliance with OSHA 29 CFR 1910.132 standard.
Red Flags of Internal Fraud, Asset Misappropriation, and Corruption
Sinai Megibow
60 Min
Product Id: 703578
This webinar will detail the variety of internal economic threats such as fraud, asset misappropriation, and corruption faced by businesses and examine the different methods and schemes by which dishonest employees target their employers. We will discuss how to identify red flags of those threats and preventive measures that companies can take in order to reduce the likelihood of being victimized.
Food Contact Notification (FCN) - Obtaining New Regulations from FDA on Your Terms
Jeffrey Scott Eberhard
60 Min
Product Id: 703572
This food safety webinar will explain how to thoroughly review a food contact substance, determine its regulatory status and obtain a new regulation from FDA via the FCN process for a substance that does not meet suitable regulatory status.
Simplifying the Dietary Supplement cGMPs for Those Confused by the Regulations
Jennifer Medlar
60 Min
Product Id: 703559
This webinar will explain cGMP regulations for dietary supplements. It will provide an overview of key requirements for dietary supplements including written procedures and records required by cGMP. Attendees will learn best practices to comply with these regulations.
Compliance Planning for HIPAA 2 - What Needs to Change in Policies and Procedures
Jim Sheldon-Dean
90 Min
Product Id: 702917
This HIPAA compliance webinar will describe the changes to HIPAA privacy and security regulations and discuss how HIPAA covered entities will have to change their related and policies to ensure compliance.
Quality System Development: Strength, Compliance and Efficiency through Value Stream Mapping
Philip Russ
60 Min
Product Id: 703490
This webinar will explain the principles of lean and value stream mapping. Attendees will learn how to apply lean concepts to continuous improvement work across the quality system.
Residual Solvents: Understanding the Requirements and Practical Advice for Implementing USP <467>/ICH Q3C
Gregory Martin
120 Min
Product Id: 701916
This training on residual solvents will discuss the regulatory landscape for residual solvents and compliance requirements, including interpretation of the majors sections (classes of solvents, options for describing levels, analytical procedures).
How to Develop a Successful ERM Program Ensuring Synergy, Transparency and System Solutions
Michael C Redmond
60 Min
Product Id: 703580
This webinar highlights the importance of an effective ERM program in project management and risk assessment. Attendees will learn how to implement a viable ERM program including documenting and testing it.
Teller Compliance Training: Reg CC, CTR and UCC 3 and 4
Kara Lamphere
60 Min
Product Id: 703523
This webinar will provide an overview of the Bank Secrecy Act (BSA) and Regulation CC. It will explain how and when to place holds on deposits. Attendees will understand red flags concerning money laundering and how to complete a currency transaction report (CTR).
Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO)
Jamie Jamshidi
90 Min
Product Id: 701065
This webinar will discuss in detail key auditing elements of an Active Pharmaceutical Ingredient (API) facility/operation. It will cover selection, designation and documentation of starting materials; qualification of analytical methods; control requirements for multi-product/multi-processing API production facility; QA review and release of API and much more.
Implementing a Whistle-Blower Program - Detecting and Preventing Fraud at Workplace
Richard Cascarino
90 Min
Product Id: 702725
This training on effective whistle-blower program implementation will discuss its importance and issues and provide tips on how to choose a reporting mechanism to detect and prevent fraud/misconduct or unethical workplace behavior both in the public and the private sectors.