IRS and State Agencies have increased their audits of workers classified as Independent Contractors. Why, because both Agencies are looking for more revenue without raising taxes.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 email@example.com Event link https://onlinecompliancepanel.com/webinar/CONTRACTOR-VS-EMPLOYEE-507063/OCTOBER-2017-ES-TRAININGREGISTRY
This course will help participants examine issues on the project from multiple viewpoints. While a General Contractor certainly has one perspective on the project, so too do the Owner, Architect/Engineer, Subcontractors, and other Stakeholders. By learning to present issues in the right framework we decrease adversarial behaviors on the project and increase the likelihood that our proposals for additional work will be accepted.
Business Administration is often very generalized and even more often overlooked by project managers. This course is targeted to teach you the strategic and business administration concepts that are specific to project management.
Too many times we try to manage our projects in a vacuum without awareness of how we impact the company overall, and how the company overall impacts our performance as project managers.
This webinar will cover what is important in facility design from the FDA and regulatory standpoint. You will understand what FDA looks for during a facility inspection. You will be able to minimize possible design errors which are difficult and expensive to fix post-build. Understand what FDA looks for in reviewing the facility design and the flow patterns.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 firstname.lastname@example.org Event link http://www.onlinecompliancepanel.com/webinar/PHARMACEUTICAL-BIOLOGICS-DESIGN-501777/OCTOBER-2016-ES-TRAININGREGISTRY
Production and Process Controls (P&PC;) are one of the key capabilities necessary for medical device companies to consistently and effectively produce products. P&PC; is critical to producing safe and effective products for your customers. It is a broad area covering environmental, personnel, contamination, building, equipment, inspection, materials, and more. Because of its criticality, P&PC; is one of areas most closely inspected by the FDA. This webinar will help you understand what is necessary for P&PC; and how to integrate it seamlessly with the rest of your Quality Management System.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 email@example.com Event link http://onlinecompliancepanel.com/webinar/PRODUCTION-PROCESS-CONTROL-MEDICAL-DEVICE-501676/OCTOBER-2016-ES-TRAININGREGISTRY
Deficient through wall flashing systems are the predominant cause of water leakage into the through the building enclosure system. The results of such leaks are building enclosure system failures, structural element failures, the growth of mold spores and fungus in building enclosure systems and degraded indoor air quality.
The presentation begins with a brief history of the evolution of through wall flashing systems. Materials and systems currently available on the market are reviewed and critiqued. A series of product specific installation details are reviewed. Finally, through wall flashing system cost data are offered along with a review of the benefits and drawbacks of the various systems discussed.
This webinar will focus on the comparison between the old and new Regulation 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.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 firstname.lastname@example.org Event link http://onlinecompliancepanel.com/webinar/THE-JOBS-ACT-REGULATION-D-OFFERING-501484/JULY-2016-ES-TRAININGREGISTRY
This webinar will introduce the overview of customs fees and special duties (including Antidumping and Countervailing) and avoid the land mines. CBP has fees and special duties which can create fines and penalties for non-compliant importers. Participants will also get answers to these questions: What is Antidumping? How does it differ from Counter-Vailing duties? What Agencies are involved in ADD/CVD matters? How can an importer stay compliant? Attend this webinar to gain tips for avoidance and mitigation of damages. Also learn rules and best practices.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 email@example.com Event link http://onlinecompliancepanel.com/webinar/CUSTOM-ENTRY-PROCESS-501469/JULY-2016-ES-TRAININGREGISTRY
Every Covered Entity and Business Associate is liable to be audited for HIPAA Compliance by U. S. Department of Health and Human Services (HHS). HIPAA Compliance Audits are now underway. HHS finalized HIPAA Compliance Audit procedures and is screening Covered Entities picked randomly from the National Provider Identifier (NPI) database to identify the first group of Covered Entities to be audited. The first group of Business Associates audited for HIPAA Compliance will be selected from Business Associates of the first group of Covered Entities. This is an enforcement audit.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 firstname.lastname@example.org Event link http://onlinecompliancepanel.com/webinar/OCR-LAUNCHES-PHASES-2-HIPAA-AUDITS-BUSINESS-501578/JULY-2016-ES-TRAININGREGISTRY
This training program on implementing an effective laboratory quality management will focus on ISO/IEC 17025 requirements. Attendees will learn how to develop and maintain a quality management system to ensure compliance with the international laboratory accreditation standard.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 email@example.com Event link http://onlinecompliancepanel.com/webinar/EFFECTIVE-LABORATORY-QUALITY-MANAGEMENT-SYSTEM-501579/JULY-2016-ES-TRAININGREGISTRY
This webinar will provide the attendees with an overview of both FDA's Low-Risk Device Draft Policy (January 2015) and guidance on Mobile Medical Applications (February 2015), along with insight as to how companies can achieve compliance with both.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 firstname.lastname@example.org Event link http://onlinecompliancepanel.com/webinar/FDAs-LOW-RISK-POLICY-MEDICAL-DEVICE-501520/JUNE-2016-ES-TRAININGREGISTRY
The United Nations Convention Against Corruption was formed as a committee in 2003 to help combat what was being seen as an epidemic against free trade. Organizations working in the international arena now face greater regulatory challenges to continue practicing, to educate their employees, and to monitor for violations. The legal loophole is spreading and the FCPA has recently held financial institutions liable for not reporting clients who fail to comply with FCPA requirements.
We manage tasks and activities, and those activities must be performed by people, who must be led. It is not enough to simply be a Project Manager. We must become Project Leaders. Much of this transformation comes from the use of our attitude.
Our attitudes are the most important tool in our toolbox. It costs us nothing to purchase, if we use it well it can gain us everything, and if we use it poorly it can cost us everything. How we use it is up to us. Participants will learn how to get the most from their project team by focusing on key attitude changes.
In 2004, the Committee of Sponsoring Organizations of the Tread way Commission (COSO), issued a principle-based guidance on designing and implementing an effective enterprise-wide approach to risk management. This guidance defines essential components - such as risk appetite, risk tolerance and portfolio view, provides guidance using common principles, and provides counseling and strategy for an effective program.
With the proliferation of the use of air barriers in building enclosure systems the potential for problems exists in the industry. This workshop will review the proper planning, product selection, specifications, details and field quality assurance needed for a successful air barrier installation.
The program starts with a list of steps to be taken during each phase of design and construction. Proper exterior wall design based on type of construction and proper material selection based on type of construction will then be reviewed. Details for specific wall construction type and product selection will be then be offered and reviewed. Poor detail examples will also be reviewed and discussed. Finally, quality assurance guidelines will be offered including pre-construction meetings, mock-up review and field inspection recommendations. Examples of problem installations will also be offered with explanations of the problems.
Continuous improvement or Kaizen is about engaging the work force through empowerment to improve performance and innovation. Success is achieved by focusing on key worker motivators. Engaging the workers is critical to a company's success in today's highly competitive marketplace.
Tom Peters has stated that "Tomorrow's victories will go the masters of innovation! Period!" What makes worker involvement critical is the fact that when companies win awards for innovation, most of the ideas come from the workers, not management.
As follow up to the Four Barriers For Four Wetting Potentials presentation, this presentation focuses on design considerations for air barrier systems. Products and systems are reviewed and critiqued. Ancillary building enclosure system components are discussed. Problematic areas of the building enclosure system are brought to attention.
The goal of the presentation is to point out critical considerations that should be addressed prior to commencing with the working drawings for a project.
It is just a fact of life that someone on your team, whether you selected them or whether they were assigned to you will be a non-performer. This may be because they are simply not performing to the level desired or it may be an issue of time management, or even an issue of motivation.
How do you know whether to keep these team members on board or replace them? How do you know if you can help them improve their performance?
This course will help participants learn specific techniques to identify potential performance issues, and specific strategies for making sure they don’t cause consistent problems with the team.
Real world examples of what to expect, and what to prepare for whenever possible. Not every organization is ready to avoid inspections or fines if they do not have senior staff in place, and/or if they have not been audited in the past.
How to train staff to have the correct documentation in place. Ensure that the organization keeps documentation updated and realistic. If an employee is nervice and informs the inspector/auditor wrong information, a strong documentation system will support all of the proper steps that are in place. What to strive for and whom to ask for help and assistance is always important.
The program starts by explaining the benefits of pre-planning. It goes on to explain why the pre-planning process must start as early as possible. There are two reasons why an early start is necessary. The first is the improved operational performance. The second, which is obviously related to first, is to improve the profitability of all stakeholders.
While most people tend to believe pre-planning is important, too many, still don't do it. Therefore, the program addresses the key obstacles to pre-planning.