Hospitality Industry

Learn how to use websites and social media for patient engagement in healthcare without violating HIPAA compliance. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/HIPAA-Violations-Social-Media-Web-Sites-Patient-Reviews-Simple-Compliance-Steps-to-Avoid-Danger-508096/MARCH-2019-ES-TRAININGREGISTRY

By attending this session you will be able to ensure that you understand the compliance issues directly related to the practice of case management and that you have incorporated them into your daily practice. Compliance includes documentation and communication with the patient and family as well. Be sure that your processes are hard-wired and part of your daily routine.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Compliance-Measures-for-Case-Managers-508519/SEPTEMBER-2018-ES-TRAININGREGISTRY

This webinar provides introductory information for banks and credit unions to work toward meeting the regulator's appraisal program requirements. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Commercial-Appraisal-Review-Focus-on-the-Tough-Ones-507165/AUGUST-2018-ES-TRAININGREGISTRY

Learn in depth about the general requirements and applicable laws in order to commercialize food products in Mexico. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Food-Laws-and-Regulations-in-Mexico-and-Functions-Procedures-508635/APRIL-2018-ES-TRAININGREGISTRY

Attending this webinar by expert speaker Deidre L. Tate, will give you a clear understanding of your responsibility for the new electronic submittal process and ramifications to the employer. The U.S. Occupational Safety and Health Administration (OSHA) have changed elements of the 29 Code of Federal Regulation (CFR) 1904 to include electronic submittal of injury and illness data. OSHA believes this is a behavioral economic move to provide a "nudge" to employer to focus on safety. The information for injury and illness will be available publicly and is believed to help accuracy of recordkeeping data.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/GET-THE-RECORD-STRAIGHT-OSHA-S-NEW-508978/NOVEMBER-2017-ES-TRAININGREGISTRY

The pharmaceutical industry has seen an increase in the number of biologics released to fight human disease. Large molecule therapeutics requires additional consideration when developing and validating supporting methods. This webinar will address steps to consider when developing bioassays with the expectation of successful completion of validation. Specifically, this webinar covers essential concepts related to cell-based potency methods, ELISA, and other methods supporting biologics. Specific topics covered in the webinar will include cell culture, multitrack development strategies, DOE, assay variability, and the validation protocol. Attendees will receive information that should be beneficial in helping to achieve well-controlled validated bioassay methods.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/BIOASSAY-DEVELOPMENT-AND-METHOD-VALIDATION-5045

The Problem: We have all heard of Data Integrity but do you really understand what it is? Do you understand how 21 CFR 11 and Annex 11 fit into this picture? Specifically, can you answer questions on the following: Evolution of 21 CFR Part 11 and Annex 11 and Why they are Back in the News Overview and Key Requirements of Part 11 & Annex 11 How to use a Risk Based Assessment to reduce work while still achieving Data Integrity and Compliance? How FDA & other Regulatory Authorities Inspect Computerized Systems for Data Integrity? I often refer to 21 CFR 11 and Annex 11 as Good Software Engineering with the Documentation on Steroids! However, unless one knows how to implement Data Integrity Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901052SEMINAR?trainingregistry-December-2017-SEO

We all have medical issues from time to time and sometime we need something over the counter or stronger that is prescribed by a physician. Though, the use of prescription drug is quite legal, the warning on the label always mentions not to operate heavy machinery while taking such medications. The risks are loud and clear. So, when can you as an employer regulate something that might be completely legal? When can an employer require an employee to disclose his/her medications and what an employer needs to do?Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/MEDICAL-MARIJUANA-AND-OTHER-PRESCRIPTIONS-508435/OCTOBER-2017-ES-TRAININGREGISTRY

Any method that must be done identically by 2 or more laboratories will have specific issues. These include variances in instrumentation, chemicals, people, training, and a dozen other significant areas. Even these are dealt with to be as similar as seems reasonable in a first attempt, differences are found. The use of specific protocols in these areas, more controlled purchasing decisions, uniform training and SOPs, routine running of round-robin unknowns as well as check standards are a few steps that tighten control further.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/DEVELOPING-TESTING-AND-TROUBLESHOOTING-509546/OCTOBER-2017-ES-TRAININGREGISTRY

The Stark law generally prohibits physicians from referring Medicare patients for Designated Health Services ("DHS") to an entity the physician or immediate family member has a financial relationship with, unless an exception applies. Under Stark, there is an exception known as the Non-Monetary Compensation ("NMC") exception (42 C.F.R. 411.357(k) that allows DHS entities that are the recipient of Medicare DHS referrals to provide certain non-cash items or services to a physician, up to $398 for 2017. This dollar amount threshold is adjusted each year for inflation.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/HOW-TO-TRACK-GIFTS-TO-PHYSICIANS-COMPENSATION-RULE-504946/OCTOBER-2017-ES-TRAININGREGISTRY

In a complex health services environment with many different health care practitioners, individual practitioners and directors at health care facilities may be confused on how long to retain -- and whether to dispose of -- medical records. Does having digital records require records to be kept indefinitely, or does it simply allow it?Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://onlinecompliancepanel.com/webinar/PATIENTS-MEDICAL-RECORD-506825/OCTOBER-2017-ES-TRAININGREGISTRY

Medical device manufacturers need to establish statistical methods to understand and improve process capability and product characteristics. These could take many forms, because there are a variety of techniques available. The application of the tools is not always clear. Incorrect choices, inadequate descriptions, or incorrect implementation can result in missed opportunities or, at worst, an FDA Warning Letter.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/LINEAR-REGRESSION-MEDICAL-DEVICE-MANUFACTURERS-502580/OCTOBER-2017-ES-TRAININGREGISTRY

All medical device manufacturers marketing in the United States must have procedures for reporting adverse events to the FDA. This applies regardless of where in the world the company manufactures the device. During an FDA Inspection, the investigator will ask for the procedures and verify that they follow the regulation. This includes linking the MDR information to complaints and reporting to FDA. Failure to implement the MDR regulations properly is one of the most common problems cited in Warning Letters. It comes just below the complaints and corrective and preventive action, both of which are often related.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/MDR-PROCEDURES-506897/SEPTEMBER-2017-ES-TRAININGREGISTRY

Validation Master Plans (VMPs) are written to guide and implement an organization with its validation strategy. The Validation Master Plan is different from a validation procedure (SOP), which describes the WHY for performing validation activities. The VMP describes the WHERE and HOW of a process validation program.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/DEVELOP-IMPROVE-MASTER-VALIDATION-PLAN-507598/AUGUST-2017-ES-TRAININGREGISTRY

This webinar will cover the new law on confidentiality of substance use disorder patient records under 42 CFR Part 2. This law was previously known as the confidentiality of drug abuse and alcohol abuse records. The new law was effective in 2017. Anyone or any facility that is subject to these requirements needs to attend this webinar.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/NEW-FEDERAL-LAW-42-CFR-PART-2-503438/AUGUST-2017-ES-TRAININGREGISTRY

The webinar will explain for HIPAA covered entities and business associates the process of drafting, adopting and implementing HIPAA compliance policies. Writing a policy is easier than one may think. It is a three-step process: Researching, drafting, and revising. This webinar will teach you to ask questions, solicit help, collect samples, keep the principles of substance, organization, coherence, style and correctness in mind while you are drafting, send your draft out for review, incorporate comments, implement the policy and repeat as necessary..Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/HIPAA-SECURITY-POLICIES-PROCEDURES-504014/AUGUST-2017-ES-TRAININGREGISTRYhttps://www.onlinecompliancepanel.com/webinar/HIPAA-SECURITY-POLICIES-PROCEDURES-504014/AUGUST-2017-ES-TRAININGREGISTRY

The classification of device accessories has a high visibility. For example, the 21st Century Cures Act, signed into law in December 2016, amends the FD&CA; to include accessory classification. It is very important, as a result, to apply the guidance document to your firm's products to determine if any of them are an accessory and as a result, ensure they meet the device regulations.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/DEVICE-ACCESSORIES-505201/AUGUST-2017-ES-TRAININGREGISTRY

The Centers for Medicare & Medicaid Services (CMS), in collaboration with public and private partners, is transforming how they conduct business and operations, connect providers and empower consumers and their beneficiaries.CMS enhances its partnerships in a delivery system where providers are supported in achieving better outcomes in health and health care at lower cost for the beneficiaries and communities they serve.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CMS-QUALITY-INDICATOR-501905/DECEMBER-2016-ES-TRAININGREGISTRY

These videos are specifically geared towards safety training for employees of hotels. Topics include housekeeper safety, laundry room safety, back injury prevention, and much more.