Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations
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How to Prepare Statement of Cash Flows

How to Prepare Statement of Cash Flows | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Understand how to properly prepare the statement of cash flows and its importance to users of the financial statements. Register for this webinar today.

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The statement of cash flows is a critical component of a company's set of financial statements. It enables users to see the cash inflows and outflows of a business as they relate to operating, investing and financing activities, and evaluate liquidity and quality of earnings. This interactive course covers the proper preparation of the statement as well as analysis techniques. Case studies and sample documentation will reinforce major concepts and help participants apply analysis techniques discussed.
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ISO 14971:2007 and EN ISO 14971:2012 Risk Management

ISO 14971:2007 and EN ISO 14971:2012 Risk Management | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Register for this 90 minutes webinar to learn the requirements for device risk management using ISO 14971:2007 and EN ISO 14971:2012.
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Risk management is essential to device design and required by other standards, such as usability engineering, biocompatibility and electrical safety. The basis is ISO 14971:2007, but many companies don't understand the standard, don't follow the process flow, and consequently don't have an effective implementation. This presentation helps you avoid the common problems and create a compliant system.
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Stability Testing for Dietary Supplements

Stability Testing for Dietary Supplements | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Attend this webinar to learn in-depth about stability testing for Dietary Supplements. Register for this training course today.
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The purpose is to present recommendation for supporting the voluntary shelf-life (expiration) dating claims of dietary supplements. The purpose of stability testing is to provide evidence on how the quality of formulation varies with time under the influence of a variety of environmental factors. Stability testing permits the establishment of recommended storage conditions and shelf lives.
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SSA Revised Medical Criteria for Evaluating Mental Disorders

SSA Revised Medical Criteria for Evaluating Mental Disorders | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Attend this webinar to learn the Social Security Administration’s Revised Medical Criteria for Evaluating Mental Disorders. Register for the webinar today.
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This webinar will discuss the new changes to Social Security Listing of Impairments 12.00 Mental Disorders.The key objective of the presentation is to make the attendees understand the new impairments and change in evaluation criteria for adult mental impairments.You must attend this webinar because there is a major change in how mental impairments will be analyzed by the Social Security Administration.
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HR Professionals Guide on ERISA

HR Professionals Guide on ERISA | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Attend this training session and gain a high level understanding of ERISA issues, as they relate to retirement and group health plans.
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Under the Employee Retirement Income Security Act of 1974, as amended (ERISA), and the continued guidance on and court interpretations of ERISA, plan sponsors must navigate a myriad of rules and regulations to confirm that their employee benefit plans are compliant under Federal law. As ERISA impacts both retirement and health plans, the new rules and guidance are far-reaching. Non-employee benefit lawyers, employers, and HR professionals must be familiar with ERISA so that they may spot certain compliance issues related to their clients’ or their own employee benefit plans.
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Device Master Record and FDA Quality Regulations 21 CFR 820

Device Master Record and FDA Quality Regulations 21 CFR 820 | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Attend this training program to learn DMR definition, DMR use in creating DHR, DMR document control, DMR changes requiring DHF and more.
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Device Master Record (DMR) is the output of design controls and the source document for every medical device. An accurate, complete DMR gives the 'recipe' for making a medical device. From the smallest component or ingredient and simplest operation or step to the finished medical device including labels, labeling, primary, secondary and beyond packaging to installation, servicing and maintenance instructions, the DMR has everything including the exact format and content of a medical device's device history record (DHR/batch record). Without a well-documented, up-to-date DMR for every medical device, a manufacturer/distributor cannot demonstrate compliance with FDA's Quality Regulations – 21 CFR 820.
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Applying NOM-086-SSA1-1994 for Food and Beverages with Modifications in Composition

Applying NOM-086-SSA1-1994 for Food and Beverages with Modifications in Composition | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Register for this informative webinar to learn how to apply NOM-086-SSA1-1994 for food and beverages with modifications in its composition.
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In this 90 minutes session, attendees will learn the Mexican standard about food and non alcoholic beverages with modifications on its composition and nutrimental specifications.This standard was created in order to attend the relationship between health and nourishment combined with the existence of numerous food products modified on its composition because of the elimination or the addition of nutriment, that's why it was necessary to establish nutrimental specifications in order to give correct information to the Consumer.
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Office 365-Working in the Cloud

Office 365-Working in the Cloud | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Learn what Office 365 is and how Microsoft Office 365 will allow you to be productive “on the move”. Register today if you wish to increase your productivity.
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Office 365 is a subscription based service from Microsoft that allows you to be productive anywhere. Not only does it give you MS Office licenses for your desktop/laptop computer, but you also get access to the powerful online and mobile versions of Office as well as 1TB of storage for your files, which you can access from anywhere on any device. This session combines background knowledge with practical demonstrations.
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Nonresident Alien Information Reporting Using Forms 1042-S and W-8

Nonresident Alien Information Reporting Using Forms 1042-S and W-8 | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Learn to identify your NRA payees and bring your company into compliance with the 30% backup withholding requirements. Register for the webinar today.
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Do you have a plan to deal with IRS demands for backup withholding if you failed to deduct from payments to Nonresident Aliens' (NRAs)? The IRS is working hard to reduce the delinquent tax burden. They know companies are becoming relatively compliant with 1099 reporting, but they also understand that companies and their advisors are less sure when it comes to identifying and performing backup withholding on NRAs. Collecting the tax due from NRAs working in the U.S. is an IRS Tier 1 audit issue. This tax burden is minimized when companies making payments to NRAs for both dependent and independent personal services properly withhold on these payments.
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Maintain Effective QMS in Medical Device Industry with Quality Audits

Maintain Effective QMS in Medical Device Industry with Quality Audits | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
2 days workshop on tools to establish and maintain an effective quality audit program for medical device manufacturing. Book Now.
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Quality management systems of medical devices have to go through well-defined quality audits. This 2-days workshop provides the tools to establish and maintain an effective quality audit program for medical device manufacturing. Join Daniel O'Leary in this training session to learn how to implement the quality audit program elements using examples and exercises that help develop the necessary skills.

Quality audits are an important element in implementing and maintaining an effective Quality Management System (QMS). Audits are one of the most powerful tools that management has to assure on effective QMS. 

 In this workshop, participants review the various kinds of audits to understand their role. Internal quality audits (1st party) help a company evaluate itself. Customer/supplier audits (2nd party) play a role in an effective supplier management program; your company could be the subject of the audit. Independent audits (3rd party) can help provide assurance about the health of a QMS.This workshop provides the tools to establish and maintain an effective quality audit program for medical device manufacturing. This includes the two major elements. First, is a plan to schedule, conduct, report, and close audits. Second, is the assignment of qualified people based on skill and considerations of conflict of interest. The workshop explains how to implement these quality audit program elements using examples and exercises that help develop the necessary skills.etc..
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How to Manage off-site Employees Effectively

How to Manage off-site Employees Effectively | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Learn how to fine-tune your off-site management skills in an environment where you don’t have to worry about making a costly mistake. Attend the webinar.
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Every manager knows that the best and fastest way to learn a new skill is through practice. That's why we've packed this hard-hitting workshop with powerful exercises, models and case studies specifically designed for managers of multiple locations.

This is a unique opportunity to fine-tune your off-site management skills in an environment where you don't have to worry about making a costly mistake. This is your chance to master proven-effective strategies that you can put to work immediately. When you take part in this workshop, be prepared to roll up your sleeves, sweat a little and think a lot. During the session, you'll examine off-site management challenges and solutions with peers; practice techniques for getting poorly performing locations up-to-speed; determine what the pros did right - and wrong in real-world case studies and much more.
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2016 NACHA Rules changes and 2017 NACHA Rules Changes

2016 NACHA Rules changes and 2017 NACHA Rules Changes | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Join the webinar and learn 2016 NACHA Rules changes like unauthorized entry charges for ODFIs and 2017 Third-Party Sender Registration rule and more.
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This webinar will cover in detail the significant 2016 NACHA Rules changes and outline the upcoming 2017 NACHA Rules Changes. Topics covered include: 2016 Significant Rules changes including unauthorized entry charges for ODFIs, changes to return thresholds for the ODFI, and the Same Day ACH requirement (which is a three-phase process Sept 2016 thru Mar 2018). The New (recently approved) Third-Party Sender Registration rule details, effective in 2017 will also be included.

Being in compliance with the NACHA Operating Rules is an important responsibility and requirement for financial institutions and companies, including third parties. Attending this webinar will help keep participants in the network on top of the changes and how to ensure they are prepared, know what a rule change means to them, and will be in compliance at the right time.
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New Anti-Bribery Management Systems Standard ISO 37001

New Anti-Bribery Management Systems Standard ISO 37001 | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
How to be in compliance with new standard on anti-bribery management systems, ISO 37001. Register for the webinar today.
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The webinar will help your organization implement an anti-bribery management system, or enhance the controls you currently have to reduce the risk of bribery occurring and can demonstrate to your stakeholders that you have put in place internationally recognized good-practice anti-bribery controls. Bribery is one of the world's most destructive and challenging issues. With over US$ 1 trillion paid in bribes each year, the consequences are catastrophic, reducing quality of life, increasing poverty and eroding public trust.
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How ADAAA, FMLA, and Worker’s Comp (WC) applies to work Situations

How ADAAA, FMLA, and Worker’s Comp (WC) applies to work Situations | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Attend this advanced training course to review the intricacies of how WC, ADAAA, and WC intersect to provide employees’ coverage under these acts. Register for the webinar now.
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The webinar addresses laws that HR is responsible for upholding. When the laws are not followed, it increases the liability for the organization and interferes with a fair and equitable work environment for employees. The interplay among Workers' Comp, ADA, and FMLA is confusing to many HR professionals; this webinar will help decipher the complexities.
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FSMA’s New Intentional Adulteration Rule and Compliance Strategies

FSMA’s New Intentional Adulteration Rule and Compliance Strategies | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Know more about the FSMA final rule requirements related to food defense under the Food Safety Modernization Act. Register for the webinar today.
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All of the most recent regulations required for food manufacturers can leave regulatory departments swimming in new programs to write or amendments to be made to current programs. Beyond ensuring that your programs are written and followed properly there are training requirements that must be met. Attendees will leave with knowledge of the final rule requirements related to food defense under the Food Safety Modernization Act. This will include links to regulatory sites and other references for further study.
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Risks and Liabilities of Joint Employer

Risks and Liabilities of Joint Employer | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Are you a join employer? Then attend this webinar to understand what are your legal risks and liabilities.
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The National Labor Relations Board, the U.S. and state Departments of Labor and a number of other agencies have been broadening the definition of the term "joint employment" to include companies that previously did not have to concern themselves with this issue. As a result, many well-intentioned employers are finding themselves making significant pay-outs that can be avoided, or at least minimized with a little bit of proactive, preventative planning. This webinar will help you understand when and how you might be a joint employer, your responsibilities and what steps you can take to better protect yourself.
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Habits of Highly Successful Supervisors-Necessary Skills Required for Supervisors

Habits of Highly Successful Supervisors-Necessary Skills Required for Supervisors | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Get trained on leadership skills and how to address critical supervisory issues necessary to becoming a successful supervisor. Register for the webinar today.
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This webinar will provide a positive, real-world approach for delivering extraordinary results. We will reveal the key components to your supervisory success! Focuses on techniques and strategies that will help you handle your job responsibilities successfully and increase your personal job satisfaction. If you need others to take direction from you in order to succeed, you will find this program of tremendous value!
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FDA Action on Antiseptic Wash Products

FDA Action on Antiseptic Wash Products | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Be thorough on FDA Action on Antiseptic Wash Products and what is next for the Industry. Register for the webinar today.
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The FDA just banned 19 active ingredients that are used in antibacterial soaps. This major regulation will have a huge impact on this multi-million-dollar industry since the FDA Rule will require companies to remove these ingredients from their products or remove the products from the market. Manufacturers will have one year to take these products off the market or reformulate them. This presentation will cover FDA Action on Antiseptic Wash Products and what is next for the Industry.
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US Customs FREE ACE Portal to Improve Import Compliance

US Customs FREE ACE Portal to Improve Import Compliance | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Learn how to establish a FREE US Customs ACE portal account, extracting meaningful reports on a timely basis and best practices for analyzing extracted data. Register for the webinar today.
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Since the US Customs Modernization Act, which entered into force in 1994, the responsibility and liability to conform to all material Customs Laws and Regulations has fallen squarely on to the Importer of Record. All US importers have the legal responsibility to "exercise reasonable care" in all aspects of their importations. Various tools such as ACE Accounts, US Customs own website, provides access to transactional import data, allowing importers to identify potential material violations, and implement corrective measures for risk mitigation. In addition, ACE extract reports can provide a window into finding data-driven strategic trade opportunities for potential enhanced bottom-line activity.
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Protecting your Financial Institution from Loss- Check Handling Rules

Protecting your Financial Institution from Loss- Check Handling Rules | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Know how to improve your financial institution’s performance. Learn best practices in Check cashing issues and protect your financial institution's reputation. Attend the webinar.
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Protecting and improving your financial institution's reputation and bottom line often begins (and ends) with your customer's interaction with the front-line personnel. Getting it right on the branch floor, with the proper training, enhances the brand's value and avoids the business risk of a death-by-a-thousand- cuts.
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Auditing and Qualifying Suppliers and Vendors

Auditing and Qualifying Suppliers and Vendors | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
How to prepare and plan for a supplier and vendor audit and how to write effective Audit Report, and more.
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The various regulatory agencies have expectations that suppliers and vendors will demonstrate control over their manufacturing processes, validations, and documentation. Quality auditing is the process of checking whether these organizations have implemented what they have stated in written procedures and whether their people are doing what the organizations procedures state they will do.

This 90 minute overview is designed for people tasked with performing external audits for their organizations. It is also for those tasked with developing, maintaining and/or improving programs for manufacturing facilities. This includes individuals that have Quality Management Systems responsibilities for making general improvements in their organization's performance specifically related to equipment, processes and documentation. The following personnel will benefit from the course.
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Risk-Based Approach to Clinical System Data Management Validation

Risk-Based Approach to Clinical System Data Management Validation | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Attend this webinar to learn the best practices in validation of software systems from SaaS, COTS, MOTs, and custom built systems and 21 CFR Part 11 expectations. Register for webinar now.
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Validation can be a confusing topic as more systems are becoming Software as a Service (SaaS) and we will cover what the requirements are for the various types of software systems from SaaS, COTS, MOTs, and custom built systems. Best practices to system validation will be discussed for clinical data systems as well as study specific validation.
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21 CFR Part 820-Applying Lean Principles

21 CFR Part 820-Applying Lean Principles | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Learn to apply the theory of Lean documents and lean configuration in following 21 CFR Part 820.
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All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. Medical device manufacturing plants, required to follow 21 CFR Part 820, have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOPs, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.etc..
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Basic s of Cash Management in ERP Systems

Basic s of Cash Management in ERP Systems | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Attend this webinar to learn more about bank reconciliations for various types of transactions, how cash flows interact with financial statements and more.
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In this webinar, participants will learn how cash flows interact with financial statements. The Instructor will help in understanding cash flows in funding strategic initiatives. They will also learn about the bank reconciliations for various types of transactions and preparation of banking relationships for a merger.

This course will cover the fundamentals of Cash Management in ERP systems such as Oracle. It will also discuss Bank statement formats and when to apply them. Challenges in reconciliation of how to handle various deposits in transit, outstanding checks, service charges, and non-sufficient fees will be addressed. The Instructor will share his experience and the challenges faced at Comcast in its preparation for its merger with Time Warner such as streamlining its zero-balance accounts and regional banks.
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Strategies for Recovering Wage Overpayments

Strategies for Recovering Wage Overpayments | Regulatory compliance training courses covering the US (FDA) regulations and European (ICH) regulations | Scoop.it
Attend this webinar to know the common causes of wage overpayments and understand how to mitigate the effects of wage overpayments. Register for the webinar now.
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Recovering wage overpayments can be a time-consuming and sometimes challenging process for payroll tax deductions professionals. State laws governing recovery of employer overpayment and adjustment of related taxes often vary from the federal rules and from state to state. Recovery may be difficult or cause hardship for employees, particularly in termination cases. Understanding your compliance obligations and responsibilities to your employees is critical.

Wage overpayments can be a source of significant cost in terms staff time spent in analysis and correction. Compliance issues and errors made during the correction process can add to the costs. Accuracy is an essential element in the payroll deductions process, but error-free payrolls are rare. A 2008 survey by CyberShift and the American Payroll Association found that 20 percent of employers reported error rates of 1 to 5 percent of payments during typical payroll processing.
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