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  • 1 Request Info

    Webinar on Identification and Quantitation of Low-Level Compounds for Impurity and Degradation Analyses

    Understand how to have a structured approach to minor component identification and quantitation of low-level compounds for impurity and degradation. 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/Identification-and-Quantitation-of-Low-Level-Compounds-for-Impurity-and-Degradation-Analyses-502236/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on Risk Based Computer System Validation

    Join this one hour webinar to learn how to integrate risk based software supplier evaluation into the computer system validation process. 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/Risk-Based-Computer-System-Validation-504574/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar On Identifying and Managing Emerging Operational Risks

    Learn how you can identify emerging risks and understand the best practices for identifying and apprehending emerging risks by joining this webinar. 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/Identifying-and-Managing-Emerging-Operational-Risks-509738/JANUARY-2019-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Regulatory Inspections - How to prepare for a visit from an FDA auditor

    This FDA audit webinar will highlight the purpose of FDA audits and scope, understanding of QSIT audit and how to develop an audit preparedness plan. It will also give understanding of what the FDA will look for at the conclusion of your audit and how to communicate with FDA before and after the 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/Regulatory-Inspections-How-to-prepare-for-a-visit-from-an-FDA-auditor-506970/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 5 Request Info

    Compliance with 21 CFR Part 11, SaaS-Cloud, EU GDPR

    Overview: This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud hosted applications. It explains how to write a Data Privacy Statement for compliance with EU General Data Protection Regulation (GDPR). What the regulations mean is described for all four primary compliance areas: SOPs, software features, infrastructure qualification, and validation. It gets you on the right track for using electronic records and signatures to greatly increase productivity and ensure compliance.
  • 6 Request Info

    Medical Devices - Complying With 820.250 Statistical Methods

    Overview: Learn how to manage Statistics including establishing a policy along with procedures relative to specific areas of applications. Highlighted are statistical techniques for: Process Validation Design Verification Design Validation Audits and Effectiveness Checks Test Method Validation Manufacturing Acceptance Sampling Plans and Inspections Trending Data Setting Specifications
  • 7 Request Info

    Strategies for Improving Effectiveness and Efficiency of your Quality Management System

    This two-day seminar will cover the essentials of an effective yet efficient Quality management system for medical device companies. An efficient and effective Quality System can be a competitive advantage for companies by leading to improved Quality and compliance as well as optimizing the cost of Quality. This seminar will get you started in setting up just such a Quality System. We'll discuss the "case for Quality" and how you can use compliance, not as an end itself, but as a means to improved Quality and reduced cost of non-compliance. In this Seminar, we will discuss: Regulatory Expectations How to plan, structure, and implement a Quality System Common problems and lessons from 483 and Warning Letters Red-flags that your QS is not effective Six essential capabilities for an effective and efficient QMS Risk analysis and management techniques Process control and performance monitoring Culture, Management Responsibility, and maturity Strategies for improvement
  • 8 Request Info

    When Conducting cGMP Regulatory Inspections 2018

    This webinar will cover the key areas of how ICH Q7 was established, it's goals and objectives, expectations of the healthcare authorities involved and practical differences that you will experience in a GMP inspection of a facility by FDA, an EU Competent Authority or PMDA.. After this event, you will be fully prepared for cGMP regulatory inspections in those countries.
  • 9 Request Info

    Webinar on Objectionable Microorganisms - Knowing What and Where You Can Find Them in Biopharmaceutical Manufacturing

    Objectionable microorganisms are considered, if discovered, harmful to the patient. By identifying and controlling these microorganisms and putting the appropriate controls in place early in the pharmaceutical manufacturing or medical device manufacturing processes problems in the patient can be prevented. This webinar will review the regulations pertaining to objectionable microorganisms, agency expectations, methods to identify objectionable microorganisms, interpreting results, and controls to put into place. By knowing, where, when, why, and how objectionable microorganisms exist, harmful consequences to the patient can be prevented. 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/Objectionable-Microorganisms-Knowing-What-and-Where-You-Can-Find-Them-in-Biopharmaceutical-Manufacturing-508673/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar on ISO 14971:2012 - Does your Current Risk Analysis Still Comply with your CE Mark Requirements?

    This webinar will benefit medical device companies planning to have a CE mark under the European Union Directive 93/42/EEC. We will discuss what is new in ISO 14971:2012 and help you avoid delays in obtaining or maintaining your CE mark for compliance to the Medical device Directive, EU Directive 93/42/EEC on Medical Devices. 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/ISO-14971-2012-Does-your-Current-Risk-Analysis-Still-Comply-with-your-CE-Mark-Requirements-507129/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 11 Request Info

    Investigating Sterility Test Failures

    Sterility testing is widely used in both the medical device and pharmaceutical industries. The pharmacopeia test is the official procedure for testing the sterility of pharmaceutical products. Despite its importance and its widespread use, many people are not aware of the limitations of the sterility test and are unsure how to proceed when a failure investigation occurs. 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/Investigating-Sterility-Test-Failures-503878/JANUARY-2018-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar on Intelligent Approach to Risk-Based Monitoring to Improve Clinical Trial QualityROs and sponsors serious about driving clinical trial qualit

    ROs and sponsors serious about driving clinical trial quality, efficiency, and oversight, are aware of the FDA guidance: "A Risk-Based Approach to Monitoring." From a practical level, how do you start your program and gain the full advantages of RBM? This course will provide opportunities to practice the necessary skills to apply a risk based approach to monitoring activities. This webinar will help you how to ensure that your data and supporting documentation are in the appropriate format to comply with regulatory authority inspection. Risk based monitoring can contribute to better oversight and more efficient use of resources of clinical studies. 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/Intelligent-Approach-to-Risk-Based-Monitoring-to-Improve-Clinical-Trial-Quality-508756/JANUARY-2018-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar on Preparing a Proactive Root Cause Analysis with the Ishikawa Fishbone Tool

    What do you do next after you have found a non-conformance? Trying to do an uninformed 'fix' could do more harm than good, if we fix the wrong thing. All we'll do is damage the credibility of our corrective action processes and create doubts about our abilities to fix the weaknesses in our Management System. By using the Ishikawa Fishbone diagram we can take a structured approach to getting to the root of the problem. 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/Preparing-a-Proactive-Root-Cause-Analysis-with-the-Ishikawa-Fishbone-Tool-508166/JANUARY-2018-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar on Biopharmaceutic Considerations in Drug Product Design and In Vitro Drug Product Performance

    This webinar will demonstrate how biopharmaceutics may be used in the rational design of a drug product to achieve a desired therapeutic objective. Furthermore, the webinar will discuss the measurement of drug product performance, in vitro, including drug dissolution and in vitro in vivo correlation. 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/Biopharmaceutic-Considerations-in-Drug-Product-Design-and-In-Vitro-Drug-Product-Performance-502689/JANUARY-2018-ES-TRAININGREGISTRY
  • 15 Request Info

    HIPAA Compliance Officer Training | HIPAA Professional 2018

    This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid gloves any more. It will also address major changes under the Omnibus Rule and any other applicable updates for 2018 and beyond. There are an enormous amount of issues and risks for covered entities and business associates these days. I will speak on specific experiences from over 17 years of experience in working as an outsourced compliance auditor, expert witness on multiple HIPAA cases, and thoroughly explain how patients are now able to get cash remedies for wrongful disclosures of private health information. More importantly I will show you how to limit those risks by simply taking proactive steps and utilizing best practices. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901507SEMINAR?trainingregistry-February-2018-SEO
  • 16 Request Info

    Webinar on Developing an Effective CAPA Management and Root Cause Analysis System

    This 90-minute webinar will include discussions on proper CAPA system maintenance, root cause analysis, documentation of the Corrective and Preventative Actions and developing a robust CAPA plan. It will give tips on how to develop CAPAs pertaining to longer term projects and ensure they stay on track. 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/Developing-an-Effective-CAPA-Management-and-Root-Cause-Analysis-System-503423/DECEMBER-2017-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on The Importance of Packaging and Labeling in Pharmaceutical Product Development: An Overview

    Pharmaceutical and life sciences companies are under an extreme amount of pressure to maintain an ever-increasing amount of regulation and legislation. With this pressure, they still need to increase efficiencies, bring new products to the market faster, reduce prices, deliver innovation, ensure patient compliance, and maintain business compliance. 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/THE-IMPORTANCE-OF-PACKAGING-AND-LABELING-IN-PHARMACEUTICAL-PRODUCT-DEVELOPMENT-509342/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar on BCBS 239 Principles of Effective Risk Data Aggregation and Risk Reporting

    COSO continues to provide guidance and establish standards for performance in risk related processes. BCBS 239 is the latest in a series of instructions which focuses on risk data aggregation. This webinar will include discussions on the risk data aggregation capabilities and internal risk-reporting practices (the Principles) that enhance risk management and decision making processes at financial institutions. 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/BCBS-239-PRINCIPLES-OF-EFFECTIVEff-RISK-DATA-AGGREGATION-AND-RISK-REPORTING-504996/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar on Cost Analysis in Purchasing

    Managing and reducing cost continues to be one of the primary focal points of business and governments today. In many organizations, more than half of the total revenue is spent on goods and services-everything from raw material to overnight mail. Maintaining a competitive position and even survival will depend on the organizations ability to use all of the continuous improvement strategies which have been developed to reduce cost across the entire supply chain for the life of the product or service. Fundamental to developing and implementing these strategies is knowledge of Cost Analysis. 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/Cost-Analysis-in-Purchasing-504101/NOVEMBER-2017-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On OFAC Sanctions Compliance: Update, Expectations and Best Practices

    This webinar provides a basic, through advanced, overview of OFAC's sanction program. Examples are drawn from real cases as well as the instructor's experience. Make no mistake, the bad guys will try and game you. If you are not prepared you will be in trouble. The bad guys want what they want and do not care if you are fined or imprisoned. 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/OFAC-SANCTIONS-COMPLIANCE-UPDATE-EXPECTATIONS-AND-BEST-PRACTICES-507271/NOVEMBER-2017-ES-TRAININGREGISTRY