Healthcare Laws/Reform

Medicare has included both Penalties and incentives to encourage participation and correct report for multiple programs. This webinar will review the programs that are currently targeted for these actions.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/MEDICARE-COMPLIANCE-501448/MAY-2016-ES-TRAININGREGISTRY

The content deviations in Medical Device Directive and Risk Management Standards continue to create confusion and implementation problems.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/RISKMANAGEMENT-ISO14971-2012-501431/MAY-2016-ES-TRAININGREGISTRY

This webinar will discuss the requirements for a system for complaint and recalls in an FDA compliant company.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/GMP-COMPLAINT-SYSTEM-501413/MAY-2016-ES-TRAININGREGISTRY

This training program will discuss the revisions to ICH E6 R2 GCP. How these changes may impact your clinical trials in terms of cost and complexity. We will also review plans for risk management, human subject protection, and data integrity. 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/HOW-TO-PREPARE-ICH-E6-R2-GCP-REVISIONS-501456/MAY-2016-ES-TRAININGREGISTRY

Instrumental liquid chromatography (HPLC method development/ UPLC method development) commonly used in the pharmaceutical, environmental, and other areas for analyses needs to comply with either Good Laboratory Practices or ISO 17025 training. 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/VALIDATING-HPLC-METHODOLOGY-501397/MAY-2016-ES-TRAININGREGISTRY

System suitability testing (SST) is required by USP and FDA to check and ensure on-going performance of analytical systems and methods. Both USP and EP have chapters with recommendations for system suitability tests that are enforced by FDA and other agencies. Related chapters have been updated by USP and EP and they also answer the question as to how much a method can be changed without the need for revalidation. Also, the USP chapter <1058> makes a statement that SST can substitute an instrument's performance qualification, but not further guidelines are given. This webinar will give a good understanding of FDA and USP requirements for system suitability testing. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/SYSTEM-SUITABILITY-TESTING-FDA-USP-501436/MAY-2016-ES-TRAININGREGISTRY

In this session Mr. Wolfe will provide a general Stark Law overview. He will also discuss best practices for auditing existing recruitment arrangements and for implementing new Non-Physician Practitioner (NPP) support arrangements under the new 2016 Stark rules. 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/NEW-STARK-RULES-2016-501425/MAY-2016-ES-TRAININGREGISTRY

This seminar will provide an overview and in-depth snapshot of the product registration and approval process for Asia Pacific, Europe, Middle East, United States, Canada, Mexico and South America. Single Registration:-$1,400.00 http://www.onlinecompliancepanel.com/workshop/PRODUCT-REGISTRATION-NAVIGATION-800011/APRIL-2016-ES-TRAININGREGISTRY

This workshop provides an opportunity to understand the issues and discuss them with your colleagues. It will help you learn the requirements, develop approaches, and execute them. Through examples and case studies you will solidify your understanding of design controls and learn how to develop procedures that define and document your approach. Many device manufacturers market in the US, the EU, and Canada - the workshop compares and contrasts the requirements to help you develop a comprehensive system. The workshop uses FDA’s Quality System Inspection Technique (QSIT) as a method to ensure correct implementation. In addition, the workshop makes use of many recent Warning Letters to illustrate potential problems and help you learn from the mistakes of others. Single Registration :- $1,400.00 http://www.onlinecompliancepanel.com/workshop/MEDICAL-DEVICE-DESIGN-CONTROL-800004/APRIL-2016-ES-TRAININGREGISTRY

The course will cover the current regulations and importance of preparing and handing sterile and hazardous pharmaceuticals. It will also review the proposed regulation concerning all aspects of handling hazardous drugs and is appropriate for medical, nursing and pharmacy workers. Understanding these regulations will allow users to future-proof their facility and employ best work practices when performing both non-sterile and sterile HD handling. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/USP800-GUIDELINES-501386/APRIL-2016-ES-TRAININGREGISTRY

This webinar will help you understand in detail Computer System Validation (CSV) and how to apply the System Development Life Cycle (SDLC) Methodology when validating computer systems subject to FDA regulations. This is critical in order to develop the appropriate validation strategy and achieve the thoroughness required to prove that a system does what it purports to do. It also ensures that a system is maintained in a validated state throughout its entire life cycle, from conception through retirement. We will discuss the phases within the SDLC, and how these form the basis for any CSV project. The importance of the sequence of steps will also be covered. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/LATIN-AMERICAN-TRADE-501303/APRIL-2016-ES-TRAININGREGISTRY

This webinar addresses the major aspects of the FDA's recently issued draft guidance entitled "Submission and Review of Sterility Information in Premarket Notification (510(k)) Submissions for Devices Labeled as Sterile - Guidance for Industry and Food and Drug Administration Staff - January 21, 2016." Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/STERILE-MEDICAL-DEVICES-501389/APRIL-2016-ES-TRAININGREGISTRY

Systems Engineering is about system thinking which states that a system is more than the sum of its parts. This is especially true for healthcare delivery. Not only the staff must do the right quality of work but also the technology, medical records, interactions among the caregivers, facilities, and hospital services must do right things such that nothing bad happens to the patients.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/SYSTEM-ENGINEERING-501404/APRIL-2016-ES-TRAININGREGISTRY

In this webinar, expert speaker Sheldon Primus, MPA, COSS will illustrate the similarities and differences of the Process Safety Management (PSM) to the Risk Management Program (RMP) programs and will show you how to be compliant with both standards. This session will provide you with the tools and tips needed to comply with both the RMP and PSM standards, and offer a practical guide to continued compliance.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/PROCESS-SAFETY-MGMT-501364/APRIL-2016-ES-TRAININGREGISTRY

This training session will dive deep into the details regarding your practice or business information technology and how it relates to the HIPAA Security Rule, in particular portable devices. The webinar will also cover areas including texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT. 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/HIPAA-BYOD-MOB-DEVICES-501277/APRIL-2016-ES-TRAININGREGISTRY

GlobalCompliancePanel Refer a Friend Program: Any Customer to 3 Referrals "Can Participate 2 Days Seminar for free of Cost This two day seminar takes the participants through HIPAA compliance from start to compliance. The presentations explain the history of HIPAA, why it came to being and its evolution. This covers what HIPAA is, what steps have to be performed to be HIPAA compliant and what HIPAA compliance is. It also provides definitions to key HIPAA terms, how to define a Business Associate and how to contract with Business Associates.

This webinar is designed to provide a comprehensive overview of impurities which must be controlled in pharmaceutical products. It will also provide detailed review of the guidance documents related to each of the categories of impurities and strategies to address each, including reporting of test results. 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/ELEMENTAL-IMPURITIES-501374/APRIL-2016-ES-TRAININGREGISTRY

This training program will discuss optimizing your packaging design for commercial and clinical products and translating a protocol into effective packaging design. Attendees will learn how to implement an effective artwork change management system. Real-life case studies and dos/don’ts for packaging and labeling for commercial and clinical products will also be discussed. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/PACKAGING-LABELING-COMMERCIAL-PRODUCTS-501363/APRIL-2016-ES-TRAININGREGISTRY

Learn how to register your medical devices and gain approval from the regulatory authorities in Brazil, Argentina and Columbia. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/MEDICAL-DEVICE-REG-APRVL-PROCESS-501335/APRIL-2016-ES-TRAININGREGISTRY

This webinar is designed to help you identify how to make the necessary changes to accommodate UDI swiftly, so you are able to sell your product once the compliance date arrives. The UDI compliance date for Class II devices sold in the U.S. is coming! By September 24, 2016, all Class II devices need to be marked with a UDI. With the volume of Class II medical devices marketed in the U.S., some estimate that new UDI publications in 2016 will approach 260,000 records. This data volume may create technical delays for you, if you aren't prepared. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/UDI-IMPLIMENTATION-501367/APRIL-2016-ES-TRAININGREGISTRY