Compliance Training Webinars for Regulated Industries

This 90-minute webinar on personnel practices and microbial control in Pharmaceutical, Biotech, and Medical Device manufacturing will cover effective ways to train personnel on gowning and personnel practices in cleanroom operations to limit contamination. This webinar will also address controlling microorganisms on process equipment and product contact surfaces.

This trade compliance automation webinar will discuss how to create, manage and sustain the “big picture” of Trade Compliance Screening Automation projects while drilling down to the specific elements that can make or break the overall effectiveness of the automation project. It will help you identify best practices for an automation projects’ effectiveness and provide visibility to the pitfalls that can lead to unmitigated risks.

This OSHA webinar will provide necessary information on how to write a Confined Space Program along with an understanding of the specifics needed to comply with the OSHA regulation 29 CFR 1910.146

This 60 minute webinar will cover the details on middle and final efforts for setting up a food safety and HACCP program for your organization. You will learn and develop skill sets to manage and influence an integrated program intended to reduce potential food safety risk.

This 90-minute webinar will re-examine the Sarbanes Oxley Act and how SME’s may respond to the legal requirements. In particular, the webinar looks at Accounts Receivable and how executives may fulfill their obligations under the Act.

This training on lawful handling of addiction in the workplace will discuss what to expect from an employee who is suffering from an addiction, when you are required to provide leave under either the FMLA or the ADA and a host of other issues.

This EU MDD webinar will help you understand and recognize the most significant changes proposed for the new European Medical Device Regulations: 2012/0266 (COD). You will learn which procedural changes your company should be making now so that you stay in compliance throughout the transition period and reduce potential delays to new product introductions in the EU market.

This 90 minute OSHA webinar training will walk you through the process that begins after receipt of OSHA citation following an inspection. The seminar will address the time frames that need to be followed, and what your rights and responsibilities are, how to calculate fines and penalties and various options available for handling statements of employees and whom to select to re-present on behalf of company.

This complimentary webinar will contain a brief overview of the macroeconomic environment and its impact on healthcare enterprises, and the challenges that healthcare entities are facing.

This 6-hr training provides a detailed understanding of process validation for medical devices approach employing IQ, OQ, and PQ. Information includes preparation of protocols and reports, application of Statistical Process Control, concepts of Design of Experiments, using attribute sampling plans, and a discussion of GHTF document on process validation.

This webinar will provide information on food allergen labeling, the requirements set forth by the U.S. Food and Drug Administration (“FDA”) pursuant to the Food Allergen Labeling and Consumer Protection Act of 2004 (“FALCPA”). It will show how foods, including dietary supplements, must be labeled to comply with federal law and regulations, and illustrate how failure to adhere to these requirements frequently results in costly delays and recalls.

In this 60 minutes webinar, you can discover the in and out of accounts receivable risks and controls in compliant with SOX. The speaker brings vast knowledge and experience to guide you through with the know-how of accounts receivable process, fraud, weaknesses, deficiencies and the efficient ways to deal with them.

This 3-hr training on South Korean regulatory compliance requirements for life science products will discuss about the regulatory structure, clinical trial requirements and the conduct of running clinical research in South Korea.

This webinar will guide you in setting up a safety committee, defining its role, setting goals and evaluating them to measure its success.

The objective of the webinar is to present you with all-inclusive information on Federal Family and Medical Leave Act. Our leading expert will also help you learn addressing employee abuse, integration of the FMLA with your company’s leave programs, and other practical concerns that you may have.

This webinar will cover the basics of OSHA ergonomics compliance and show you what to do, step-by-step, to ensure your ergonomics program is in compliance and the company is protected from citations, penalties, and enforcement actions from OSHA.

This webinar will examine and highlight differences among non-inferiority (NI) trials, equivalence, and superiority study objectives and designs. It will also review current FDA guidance for NI clinical studies.

This 3-hr virtual seminar will help you understand the requirements of OSHA PSM and NEP audit topics that have been interpreted and reviewed in the compliance guidelines as they might apply to an anhydrous ammonia refrigeration plant.

This webinar will train you on interpreting FDA's new guidance document on risk-based monitoring. It will include a case study demonstration on how any biopharmaceutical, medical device, and CRO could leverage the applications of breakthrough techniques to implement risk-based monitoring.

This 90-minute 510(K) training will provide practical tips and tools (templates) for preparing regulatory marketing submissions that will ensure swift clearance of your Class II and Class III medical devices.