Electronics & Semiconductors - Maintenance Training

In this 90-minute session, the different types of Third-Parties will be addressed. Third-Party Service Provider and Third-Party Sender and the difference between the two will be identified to help the ODFI in determining if they have a Third-Party Sender relationship. The ODFI is required, with this new Rule, to register any Third-Party Sender relationship or even if there is no relationship, registration is still necessary.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/OUTLINE-DETAILS-THIRD-PARTY-SENDER-508949/JUNE-2017-ES-TRAININGREGISTRY

Did you know that Electronic Health Record (EHR) can be used in prospective clinical investigations of human drugs, biologics, medical devices and combination products regulated by the US Food and Drug Administration (FDA)? This includes foreign studies used in support of an application for marketing approval of the medical product. This webinar will discuss FDA's current recommendations on using Electronic Health Records in prospective clinical investigations of human drugs, biologics, medical devices and combination products. A refresher on key requirements for Computer Systems used in Clinical Investigations is also included.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/EHR-FDA-CLINICAL-INVESTIGATIONS-505427/JUNE-2017-ES-TRAININGREGISTRY

This webinar discusses current topics, considerations, and controls necessary for the implementation and validation of EBR. Electronic batch record systems (EBR) are increasingly commonplace in pharmaceutical and biotechnology manufacturing environments. EBR systems are used for the automation of the execution of a batch record; they can be interfaced with many different types of systems, equipment, and instruments.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/ELECTRONIC-BATCH-RECORDS-502288/JUNE-2017-ES-TRAININGREGISTRY

This presentation will focus on instructing attendees on best practices for buying COTS (Commercial Off-The-Shelf) software and evaluating software vendor(s). Presentation will highlight essential data and systems subject to Part 11 & Annex 11 (ERES - Electronic Records and Electronic Signatures) compliance while listing requirements for IT infrastructure, Laboratories, Manufacturing/ Operations, R&D, Regulatory and other GxP relevant areas of an FDA regulated manufacturer. 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/COTS-SOFTWARE-AUDIT-VENDORS-505707/MARCH-2017-ES-TRAININGREGISTRY

This webinar will discuss the best practices which will help ensure effective and compliant management of electronic business records. It will also discuss what the law and regulators require for FDIC, record retention, evidence and other pertinent information.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/ELECTRONIC-BUSINESS-RECORDS-509353/MARCH-2017-ES-TRAININGREGISTRY

In this webinar, you will learn the required contents of Module 3 as well as the appropriate formatting. Lifecycle management and updating requirements will be discussed, including appropriate change control and sponsor notifications. You will also gain an understanding of contact points with the FDA throughout the lifecycle of the DMF, including information requests and inspections.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/DRUG-MASTER-FILES-DMFs-509436/FEBRUARY-2017-ES-TRAININGREGISTRY

Attend the webinar to get a proper contrast and comparison of GMP and Good Laboratory Practices (GLPs), CFR part 58, for conducting nonclinical laboratory studies that support applications for research or marketing permits for products such as food and color additives, human and animal drugs, medical devices for human use, biological products and electronic products that are regulated by the FDA.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/GOOD-LABORATORY-PRACTICES-GMPs-501833/NOVEMBER-2016-ES-TRAININGREGISTRY

This webinar will provide the requirements to develop a world class lockout/tagout program to be in compliance with safety regulations and standards.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/WORLD-CLASS-LOCKOUT-TAG-SAFETY-PROCEDURE-WORKPLACE-501652/OCTOBER-2016-ES-TRAININGREGISTRY

The US Food and Drug Administration (FDA) holds cosmetic manufacturers and distributors responsible for the safety and quality of their cosmetics. This webinar serves to guide cosmetic manufacturers and distributors as well as other entities such as color additive manufacturers and analytical and microbiological laboratories on FDA recommendations and requirements concerning the safety and quality testing of cosmetics.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/COSMETIC-US-FDA-COMPLIANCE-501764/OCTOBER-2016-ES-TRAININGREGISTRY

This presentation will help healthcare providers learn how to make best use of the automated coding tools found within their EHRs. This will help with coding accuracy, helping to prevent providers from selected codes that are above or below the actual level of service for an encounter.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/EVALUATION-MANAGEMENT-CODING-EHRs-501730/SEPTEMBER-2016-ES-TRAININGREGISTRY

This webinar will help you keep abreast of developing legal trends and supervisory priorities in order to position your bank or credit union to best master electronic commercial payment orders, ACH and wire issues under UCC 4A.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/2016-PLANNING-UCC-ARTICLE-4A-501721/SEPTEMBER-2016-ES-TRAININGREGISTRY

This course will cover considerations and requirements when selecting an Electronic Quality Management System (E QMS).Due to the current climate of regulatory compliance there is a need for companies to select the appropriate electronic quality management systems (E QMS).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/SELECTING-E-QMS-SYSTEM-501443/AUGUST-2016-ES-TRAININGREGISTRY

Centers for Medicare and Medicaid Services (CMS) has issued the final rules for implementing Stage 3 "meaningful use" (MU) standards for the Electronic Health Record Incentive Program. This program adjusts payments to Medicare and Medicaid providers for implementing and "meaningfully using" (or not) interoperable electronic health records (EHR) systems. This means that doctors and hospitals will need to evaluate how to meet the tougher requirements but benefit from reduced requirements for certain standards.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/FINAL-RULES-ELECTRONIC-HEALTH-501422/JULY-2016-ES-TRAININGREGISTRY

When validated methods are transferred between laboratories and sites, their validated state should be maintained to ensure the same reliable results in the receiving laboratory. For a long time there was no official guidance on what exactly is expected to maintain 'the validated state'. Now the USP has published an updated general chapter <1224>.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/TRANSFER-ANALYTICAL-PROCEDURES-USP-1224-501440/JUNE-2016-ES-TRAININGREGISTRY