Events

  • Regulatory Update Webinar

    In this webinar, federal regulatory actions released in 2016 that could impact water and wastewater systems will be summarized, with an emphasis on what systems could be doing now to be better prepared. Expected regulatory actions in 2017 and 2018 will also be ...


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  • Optimizing a combined Remedy Using Traditional and High-Resolution Techniques

    A Superfund Site case study will be used to highlight ways that a combined remedy at a chlorinated solvent site can be optimized to accelerate the remediation timeframe. The remedy at this site is a combination of vapor extraction, excavation, in-situ chemical oxidation, and in-situ enhanced bioremediation. This webinar will include advice on radius of influence confirmation and high-resolution ...


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  • Lead and Copper Control with Phosphates

    This webinar will cover the current U.S. EPA lead and copper rule regulation and the use of phosphates to help meet this regulation. Choice of phosphate products as well as dosage required for a distribution system will be discussed. Phosphate feed systems and safety considerations will be covered in detail based on the type of phosphate chosen for a system. Case studies showing the successful ...


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  • Webinar on Social Media Recruiting Strategies for Facebook, Twitter and LinkedIn

    This session focuses on clarifying the importance of social media, providing insight into how to effectively begin the process of incorporating social media into your recruitment strategies, and a number of specific tips and suggestions (in how-to format) on how you can begin utilizing Twitter, LinkedIn and Facebook to help meet your hiring needs, as well as suggestions on coordinating your ...


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  • Webinar on Use Payroll Pay Cards, Not Pay Checks – Save Costs and Maintain Compliance

    This interactive 90-minute webinar, presented by payroll consultant Mark Schwartz, covers the why’s, how’s, and regulatory issues regarding paycards. Mr. Schwartz will provide information about paycard providers, so you can make an informed decision on choosing the right one for your company. Areas Covered in the Session : What is a paycard and what are the benefits to an employer and its ...


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  • Webinar on Being Prepared for a HIPAA Audit

    Attendees will leave the course clearly understanding of all the requirements that must be in place for HIPAA and how to demonstrate compliance if audited. After completing this course, a Covered Entity or Business Associate will be able to know what needs to be place when it comes to all of the HIPAA regulations. Areas Covered in the Session : Why was HIPAA created? What are the HIPAA ...


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  • Webinar on Year End 2016 – Preparing for Payroll

    This webinar will also assist the W-2 new comer to understand all the boxes on the form W-2 and what should be reported. A brief overview of year end and W-2 best practices will also be discussed. Areas Covered in the Session : W-2 Requirements W-2 box by Box review Updated legislation to consider for W-2 and 2016 State by State discussion of special W-2 considerations Year End ...


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  • Webinar on Auditing to ISO 9001:2015

    The webinar will review ISO 9001:2015 clauses 4 through 10 with special emphasis on requirements that are new or different than ISO 9001:2008 clauses 4 through 8. Also to be discussed is how to determine which aspects of the existing QMS meets the new standard and do not require substantial revision. Areas Covered in the Session : A high level overview will be provided of the clauses below ...


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  • Webinar on Statistics and Data Analysis for Auditors

    In this course we provide an expansive review of sections V.c, V.d, V.e of the CQA body of knowledge. Areas Covered in the Session : Participants will learn practical application of the following concepts: Statistics - Overview Normal distribution Special and common cause variation Sampling Measures of population centering and ...


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  • Webinar on FDA Labeling Requirements – New Regulations

    Companies in the regulated life sciences industries must develop and implement systems and processes that will ensure compliance with these standards for their global labeling content. They must also take a longer-term view as to how best to minimize the complexity and cost of doing so. In this webinar, we will discuss ways to overcome these regulatory challenges and understand how companies in ...


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  • Webinar on Process Capability Analysis using Confidence or Reliability Calculations

    The seminar begins with a discussion of relevant regulatory requirements, as motivation for calculating “confidence/reliability”. Then, some vocabulary and basic concepts are discussed. All the above is captured in these bullet points: Regulatory Requirements Vocabulary and Concepts Attribute Data Normal Data Normal Probability Plotting Non-Normal Data that can be ...


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  • Webinar On Are you ready for the next FDA inspection? – Inspection Readiness Preparation

    Have you done everything you can to prepare for your next FDA Inspection? Do you have an SOP for Regulatory Inspections? Do your employees know what to do when they get that phone call from security or a receptionist? Who should security/receptionist call when FDA arrives unannounced at your firm? That’s right, FDA does not schedule an inspection – they just show up, present their credentials and ...


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  • REACH RoHS Roundup: An End of Year Update on EU Regulatory Policy as it Applies to Product

    While the US presidential election and Brexit have loomed large in recent months, requirements concerning EU substance-related legislation have continued to progress. This webinar will review the latest developments including: Revisions to the RoHS Directive concerning scope, spare parts, exemptions, global standardisation and timings plus potential new substance restrictions under ...


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  • Webinar on How to Prepare Yourself for FDA’s on-going Part 11 Inspection Program

    FDA continues to enforce Part 11 through its new Part 11 inspection and enforcement program. Just in the last 3 years, FDA issued more than 30 warning letters with Part 11 violations. Citations are related to inadequate integrity, security and availability of electronic records but also related to validation of software and computer systems. There are many questions about the program, e.g., what ...


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  • Webinar on US FDA 510(k) – Latest Guidance, Due Diligence, Preparation, Submission and Cle

    This presentation will greatly help you streamline your 510(k) preparation and submission process at your firm for maximum benefits in a least burdensome, effective manner, in accordance with lastest guidance. In this presentation, the speaker will share his PASS-IT solutions based on what he has learned from his own experience including his recent analysis of various different types of 510(k)s ...


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  • Webinar on How to conduct Annual Product Reviews to achieve GMP Compliance

    This webinar will give a brief overview of the general procedure for the preparation and documentation of the Annual Product Quality Review and also focuses on the regulations and the regulatory requirements as per US and Europe. Areas Covered in the Session : Annual Product Review Overview How to write APRs What needs to be included in the report Outline the requirements for APR ...


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  • Webinar on Effective Standard Operating Procedure (SOPs) Development for Regulatory Compli

    You will learn and understand about written procedures, and why they are beneficial. Our speaker will also cover important subjects such as FDA expectations for written documents and regulatory requirements, implementation of a training program for creating and reviewing documents, development of a system for controlling, archiving and disposing of written proposals, and development of an ...


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