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Courses

  • 1 Request Info

    Webinar on How to go Paperless in an FDA-Regulated Environment

    Learn how to go paperless in an FDA-Regulated environment using electronic workflow signature approvals and electronic records. 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-go-Paperless-in-an-FDA-Regulated-Environment-using-Electronic-Workflow-Signature-Approvals-and-Electronic-Records-503697/JULY-2019-ES-TRAININGREGISTRY
  • 2 Request Info

    Finding Causes and Selecting Solutions for Human Error

    The expectations of customers and other stakeholders is that organizations will design robust processes, and if failures occur the response will be sufficiently effective so that there will not be recurrence. Unfortunately, problems involving human error often don't get the attention they deserve. Diagnosing human error should not be a random search, but instead an organized process conducted using flowcharts, typologies and/or checklists. This webinar will provide examples of the use of these techniques in order to have a more sound investigation.
  • 3 Request Info

    Developing a Professional Reputation Using LinkedIn

    Overview LinkedIn is a business tool, not just a social media site. The focus of LinkedIn is business professional networking, research and knowledge through the LinkedIn Publishing system. The ability to find people and organizations globally, across dozens of industries, rivals business tools like Hoovers, Reference USA and Dun and Bradstreet in many ways. The added advantage of being able to see how we are connected to these people and organizations, as well as to connect directly to them makes LinkedIn a very powerful business tool.
  • 4 Request Info

    Software Validation for the New FDA Inspections

    Overview: This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation. How software requirements are used in validation will be described. This course is NOT a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.
  • 5 Request Info

    Webinar on Essentials of IT Auditing for the Non-IT Auditor

    Training is to provide the basic knowledge for non-IT auditors to allow them to do a basic IT audit during a financial or an operational audit. Subscribe now. 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/Essentials-of-IT-Auditing-for-the-Non-IT-Auditor-507775/APRIL-2019-ES-TRAININGREGISTRY
  • 6 Request Info

    Diversity and Inclusion 101

    Diversity and inclusion are common buzzwords these days but few understand what they really mean or entail. In this webinar, we will explore what diversity and inclusion REALLY are as well as common myths and misconceptions. We will discuss everything from implicit and explicit bias, diversity in areas you haven't thought of, intent vs. impact, and calling in vs. calling out and more. Participants will explore their personal relationship with systems of privilege and oppression and leave with actionable ways to increase their inclusive practices, both as individuals and members of organizations. We will explore the history of diversity and inclusion, how structural inequality has led to the marginalization of communities in the United States, and the future of D & I trends.
  • 7 Request Info

    Artificial Intelligence (AI) in the Food Supply Chain - Current and Future Potential

    Overview From robotic planting and harvesting systems through self-driving trucks, inspection systems, traceability, robotic pick and place loading systems, robotic grading systems, food processing systems, pick and place, inventory control and other areas, Artificial Intelligence (AI) is planning major changes that will impact the food supply chain in ways we can only imagine.
  • 8 Request Info

    How Blockchain Will Become the Basis for An Integrated Food Safety System (IFFS) ?

    Overview This webinar will discuss how blockchain will impact the food industry and how the likely food safety and quality inputs to this invoicing system are likely to determine your company's financial future. Various concepts will be described such as chain of custody, smart contracts, Hyperledger. Know how your company will be impacted and how to Prepare to fulfill input requirements.
  • 9 Request Info

    Webinar on Implementing ISO/IEC 27001/GDPR Compliance & Reduce Data Breach Risks

    This webinar will provide you information on how to determine data breach risks and comply with GDPR mandates by implementing ISO/IEC 27001. 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-ISO-IEC-27001-Can-Help-Achieve-GDPR-Compliance-Reduce-Data-Breach-Risks-503784/MARCH-2019-ES-TRAININGREGISTRY
  • 10 Request Info

    Turn a Culture of Quality Into a Competitive Advantage

    Overview: A culture of quality is a powerful tool for creating an effective and efficient Quality Management System. A culture of quality is not accidental but can be purposefully nurtured and developed. Why should you Attend: Every organization has stakeholders. Your customers demand safe and effective medical devices. The regulators expect you to follow the regulations for your markets with resulting product quality and compliance.
  • 11 Request Info

    Webinar ON Creating a Cyber Incident Response Program That works

    In this webinar you will learn how to develop a CSIRT Policies, Program, Plan, Playbook, full Red Team Blue team Training, table top tests and Exercises. 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/Creating-a-Cyber-Incident-Response-Program-That-works-507005/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 12 Request Info

    Seminar on Validation and Troubleshooting of Pharmaceutical Water Systems

    This course is designed to provide a microbiology-focused education about all aspects of water systems and how biofilm manages to thrive there. Prior microbiological education or training, though a plus, is not a requirement because engineers and other non-biologists also need this training if they are involved with any aspect of water systems. The instructor will provide the necessary background needed to understand this very important subject matter. This understanding is essential to the proper design, validation, operation, monitoring, maintenance, troubleshooting, and excursion investigations of a high purity water system. Without this understanding, water system control consists of a set of rules that often don't work and can cause very costly system downtime or even product recalls, and leaves the user without a clue as to what went wrong More: https://www.globalcompliancepanel.com/seminar/a-to-z-microbial-control-monitoring-validation-901945SEMINAR/?SEO
  • 13 Request Info

    Seminar on Applying ISO14971 and IEC62304 - A guide to practical Risk Management

    Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all necessary steps to design, implement and test critical medical devices in a regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management. To comprehensively summarize all risk related activities and to demonstrate the safe properties More: https://www.globalcompliancepanel.com/seminar/applying-ISO14971-and-IEC62304-901942SEMINAR/?SEO
  • 14 Request Info

    Webinar On Self Auditing Your Cyber Security Program to Mitigate Risks

    Learn how to audit ISO 27001 and Inforation/Cyber Security and manage the security assets by third parties through an effective auditing program. 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/Self-Auditing-Your-Cyber-Security-Program-to-Ensure-Risk-Mitigation-503264/JANUARY-2019-ES-TRAININGREGISTRY
  • 15 Request Info

    Complaint Handling 2019

    The information obtained will enable preparation of effective internal systems for receiving, investigating and responding to product complaints during both the investigational and commercial stages. The webinar will address aspects of the review process, SOP preparation, investigation documentation, and response to complainants.
  • 16 Request Info

    Risk Based Incident Management and [CAPA for GxP] Operations

    The CAPA process captures those incidents and failures escalated from the incident management and periodic review processes. These are then tracked from initial occurrence, through impact assessment to resolution and implementation of the correction, recognizing that the control of the resolution and implementation of the correction may be managed by other processes.
  • 17 Request Info

    Webinar on EU General Data Protection Regulation (GDPR): Compliance for Drug development and Clinical Trials

    Attain an understanding of the General Data Protection Regulation (GDPR). Be able to understand the key of the main tenets of GDPR which impact on clinical trials. Consider data breaches. Understand the role of the Data Protection Officer (DPO). 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/EU-General-Data-Protection-Regulation-GDPR-Compliance-for-Drug-development-and-Clinical-Trials-504942/NOVEMBER-2018-ES-TRAININGREGISTRY
  • 18 Request Info

    Record Keeping Best Practices [FDA and EMA] Documentation

    Overview: Good documentation Practices (GDP) is an essential factor that needs to be closely followed by the personnel in any regulated environment as a process for a successful project completion including observations of unanticipated responses that are required to be accurately recorded and verified. This one-day workshop covers the essentials of GDP, its definition, purpose, and importance. Then expands on general rules and principles of GDP (US & EU), General tips for Laboratory Notebook documentation and finally discussing GDP enforcement by regulatory bodies in different countries with some examples of FDA citations and warning letters for different points presented in the session.
  • 19 Request Info

    Webinar on Business Associates 2018 - 5 Top HIPAA Compliance Priorities

    HIPAA law applies to Business Associates in healthcare - BAs are organizations that create, receive, maintain or transmit Protected Health Information (PHI) - on behalf of a Covered Entity or to provide a service or function involving PHI for a covered Entity - and are directly liable for compliance with HIPAA law protecting the privacy and security of PHI. Price:$160.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Business-Associates-2018-5-Top-HIPAA-Compliance-Priorities-503760/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar on Conducting Internal Investigations

    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