Compliance Training Webinars for Regulated Industries

This BYOD and information security webinar will help you explore the current state of BYOD in the workplace, the need to evaluate the risk to the organization prior to deployment, the critical need for identifying and communicate a strong legal strategy, select the right mobile device management solutions (based on risk assessment), ability to develop and implement strong BYOD policies, is BYOD right for your organization, and how the “Cloud” impacts information security with BYOD.

This webinar will discuss the various safety metrics used to measure safety performance, what they really measure, and why tracking metrics often does not deliver the improvements in performance desired.

This 90-minute training will discuss recent OFCCP enforcement trends and regulatory initiatives and review these against your current practices and procedures to ensure your company is audit ready. It will also cover the proactive steps that federal contractors can take to prepare for the impending rules.

This comprehensive training package of 6 courses is aimed at helping pharma/drug companies to be compliant and streamline the supply chain planning, processes, risk management etc by maintaining regulatory guidelines.

This webinar on business continuity planning for healthcare organizations will discuss the major drawbacks to business continuity planning projects as they are currently done, and describe a simpler, more efficient approach to getting them done and implemented.

This medical device process validation training will use recent warning letters to explain the regulatory requirements for process validation and what FDA Investigators look for. It will cover process validation components (IQ, OQ, and PQ), and the content of protocols and reports.

This training on C-TPAT will explain why and what you need to do to participate in the C-TPAT (Customs-Trade Partnership Against Terrorism) program. It will cover all aspects of the C-TPAT program and help existing members to prepare for validation or revalidation.

This OSHA 29 CFR 1910.147 compliance training will explain how to create and implement an effective Lockout/Tagout (LOTO) program in the workplace that safeguards employees from hazardous energy surges.

This medical device 510(k) training will explain the basics of 510(k) submissions and discuss tips, strategies and tools to develop and execute an approval strategy ensuring the fastest possible path to market.

This 90-minute webinar will help you review your HIPAA compliance policies, and procedures to see if you are prepared to meet the changes in the HIPAA privacy and security regulations that were finalized by the end of Summer, 2012 and went into effect just 60 days later.

This webinar will familiarize you with FDA requirements for electronic and digital signatures, and the agency's inspection and enforcement practices. Particpants will recieve complimentary hand-outs for easy implementation.

This webinar on information security assessment will highlight the principal steps/ methodology for performing a third party information security assessment.

This 3-hr virtual seminar will present an overview of new risk oversight expectations and reporting rules in place, and show how companies, risk managers and internal auditors can meet these regulatory expectations.

This webinar will show how to easily interpret the FAA guidance material to create the manuals - Repair Station Manual (RSM), Quality Control Manual (QCM), and Training Program Manual (TPM) - that form the basis for the approval of new repair station certificates and continuing compliance for current repair station certificate holders.

This webinar on microbiological sampling for foods will address fundamental approaches to sampling, from raw materials to finished products. Topics will include sampling plans, sample collection methods and chain of custody issues. A primary focus will be on interpretation of results, based on the limitations of sampling plans and microbiological methods.

This webinar highlights the evolution in methodologies for forecasting trade credit bad debts. Many companies have relied on historical data or a flat percentage of sales to help forecast future credit losses. However, these methodologies don’t allow for changing markets, customer growth, or even increasing geographical diversity. A more accurate measure of future bad debt would examine your existing customer risk and determine what these risk elements tell you about the future possibility of credit losses.

This webinar will help you understand the industry background to the current transition to Risk-based Verification processes and the current trend in implementation by industry. You will learn the regulatory foundations, industry guidance, and primary components of risk-based verification as it relates to an overall specification, design, and verification program as outlined in ASTM E-2500-07; “Standard Guide for Specification, Design and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment;” ASTM, 2007. Key implementation considerations and initial steps will be discussed.

This webinar will help you to understand OSHA’s fall protection requirements and which ones apply to you. It will also guide you in selecting the best option, for the work being done, from among the various approaches to fall protection.

This training will cover HIPAA compliance requirements for Electronic Health Records (EHR) including Stage 1 and Stage 2 Meaningful Use Attestation.

This webinar will discuss how to manage supply chain risk to optimize clinical trial supply and also manage demand side requirements, risk of stock out, cost management etc using novel tools and technologies.