Regulatory & Compliance

Overview In this webinar expert speaker's James Zack will help you to identify several types of owner claims against contractors and the elements of the burden of proof required of all claimants. The basic requirements concerning damages are covered. The webinar will conclude with an outline of various dispute resolution methodologies.

Learn how to prepare for FDA inspection techniques on laboratory controls. 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/Laboratory-Controls-Anticipate-the-Systems-Based-FDA-Inspection-503311/MARCH-2019-ES-TRAININGREGISTRY

This webinar will provide valuable guidance on how to use extraction techniques to validate the cleanliness of a device. 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/Cleaning-Validations-Using-Extraction-Techniques-504912/MARCH-2019-ES-TRAININGREGISTRY

Learn the key differences between NAFTA and USMCA, legal requirements, and the custom clearance process. 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/From-NAFTA-to-USMCA-Key-differences-505468/MARCH-2019-ES-TRAININGREGISTRY

This webinar discusses how the FMEA risk assessment tool should be applied based on a case study of a sterility testing isolator. 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/Applying-FMEA-risk-assessment-to-a-sterility-testing-isolator-508790/MARCH-2019-ES-TRAININGREGISTRY

This webinar will explain the FDA process for molecular diagnostics and the regulatory requirements for each part of the process. 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/FDA-s-Regulation-for-Molecular-Diagnostics-508580/MARCH-2019-ES-TRAININGREGISTRY

This session will provide you information with procedures for controlling electronic signatures and electronic records and how 21 CFR Part 11 is connected with this area. 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/21-CFR-Part-11-Electronic-Record-and-Signature-Validation-509394/MARCH-2019-ES-TRAININGREGISTRY

Learn various useful techniques for studying stability and determining the shelf life of a product with the resulting data. 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/Stability-Studies-and-Estimating-Shelf-Life-with-Regression-Models-509644/MARCH-2019-ES-TRAININGREGISTRY

This webinar is designed to provide participants with a lifecycle approach to developing and validating analytical methods and comply with compendial 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/QbD-Approach-to-Analytical-Method-Lifecycle-Design-Development-Validation-Transfer-504438/MARCH-2019-ES-TRAININGREGISTRY

This course provides guidance on tools to plan and execute test method validation and transfer also a comprehensive overview of the international regulatory authority 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/Analytical-Method-Validation-and-Transfer-506228/MARCH-2019-ES-TRAININGREGISTRY

How to craft a Request for Proposal (RFP) with confidence? Join us to get tips on preparing RFP’s and scoring matrixes and how to avoid common pitfalls. 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/Effective-Tender-RFP-Preparation-Evaluation-Techniques-for-Today-s-Competitive-Markets-505819/FEBRUARY-2019-ES-TRAININGREGISTRY

This training program will provide in depth understanding of risk metrics applicability and discusses the sampling of forms of risk metrics to be employed 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/How-to-Establish-Review-Your-Risk-Metrics-Effectively-504188/FEBRUARY-2019-ES-TRAININGREGISTRY

Get an overview of the regulations as they pertain to the manufacturing, marketing, distribution and other operational activities engaged by companies in the tobacco industry. This course will describe the best practices for developing a compliance strategy, including roles and responsibilities, and the policies and procedures that should be followed to ensure compliance.Price:$150.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Tobacco-Industry-Trends-for-Computer-Systems-Regulated-by-FDA-508423/JANUARY-2019-ES-TRAININGREGISTRY

Regulatory expectations are clear about manufactures' responsibility regarding supplier quality oversight. All regulatory agencies agree that pharmaceutical and medical device manufactures are responsible for ensuring their suppliers adhere to quality standards, maintain compliance to regulatory requirements and consistently meet established expectations 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/Establishing-a-Robust-Supplier-Management-Program-505529/NOVEMBER-2018-ES-TRAININGREGISTRY

The webinar provides insight on how to manage marketing strategies that use social media. A firm's use of social faces FDA restrictions and obligations on how you use social media, what you can say and what you must do to correct misinformation published by third parties that places you at risk with FDA. 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/FDA-s-Off-label-Promotion-in-Social-Media-504678/NOVEMBER-2018-ES-TRAININGREGISTRY

The webinar will cover changes in the FIRRMA,how they apply to current standards, the impact of FIRRMA on existing and future transactions, the change in potential reviews from specific company actions to industry wide impact, and the overall impact that a transaction may have on national security interests. We will also examine the potential impact of Government Action in public and private transactions and how such impact may be mitigated. 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/Understanding-the-Foreign-Investment-Risk-Review-Modernization-Act-508330/SEPTEMBER-2018-ES-TRAININGREGISTRY

FDA inspections look for noncompliance with applicable manufacturing regulations. During the inspection the FDA investigator makes a "list of observations" that gives examples of violations. The list is known as the "483." Some observations are very serious and can easily lead to receiving a Warning Letter, which threatens legal action. Your response to a 483 plays a critical role in how the agency will evaluate the inspection. A poorly written response or not responding at all will certainly lead to a Warning Letter and follow up action by FDA. 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/Managing-the-FDA-form-483-Inspection-Observations-503502/SEPTEMBER-2018-ES-TRAININGREGISTRY

This topic is focused on the use of mobile applications to process data regulated by FDA. These applications may be used to collect, analyze, transfer, report, or otherwise manage data that will be submitted to FDA and/or must be available for FDA review upon inspection or audit. 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/Mobile-Applications-and-Computer-Systems-Regulated-by-FDA-508531/SEPTEMBER-2018-ES-TRAININGREGISTRY

This presentation takes you through the process of conducting an internal investigation. Some of the topics that may be discussed are: documenting predication, followed by the legal elements of such an investigation, internal and external document collection and analysis, how to interview a witness, the admission seeking interview, concluding the investigation and testifying as a fact witness. 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/Conducting-Internal-Investigations-504038/SEPTEMBER-2018-ES-TRAININGREGISTRY

This webinar will examine in detail what the regulations say about the content banks should have in an appraisal policy. Even more importantly, it will provide insight into how the regulators expect those policy statements to flow through to the overall credit decision environment and the day-to-day operations of the appraisal function. The focus will be on practical take-always from an appraisal policy consultant. 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/How-to-Have-Regulatory-Compliant-Appraisal-Policy-504004/SEPTEMBER-2018-ES-TRAININGREGISTRY