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  • 1 Request Info

    Medical Device Registration and Approval Process for the Pacific Rim 2017

    Classification systems differ from that of the United States or European Union in select countries Medical devices are classified depending on their risk level Medical devices must also comply with additional country standards and these standards define industry-wide safety and performance requirements Regulatory registration process is defined for China, Hong Kong, India, Japan, South Korea, Taiwan, Singapore and Australia The regulatory process from product design to market entry for a new medical device or IVD is oftentimes complicated and unclear. In Asia Pacific, it can become difficult to make a clear distinction between your regulatory strategy and business strategy. And Much More... Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900990SEMINAR?trainingregistry-November-2017-SEO
  • 2 Request Info

    Certificate in Cybersecurity

    The Certificate in Cybersecurity program is a suite of online courses offering information security training in Asset Security, Communications and Network Security, Identity and Access Management, Security and Risk Management, Security Assessment and Testing, Security Engineering, Security Operations, and Software Development Security.
  • 3 Request Info

    Tougher Import Rules for FDA Imports in 2017

    FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and adherence to government procedures. Firms that fail to understand and properly execute an import and export program find their shipments delayed, detained or refused. As of December 2016, FDA and CBP officially implemented the Automated Commercial Environment (ACE) entry filing system. You either meet ACE requirements or face entry refusals and monetary penalties of up to $10,000 per offense. Other factors can derail the expectation of a seamless import entry process. The course covers detailed information about the roles and responsibilities of the various parties involved with an import operation and how to correct the weakest link(s) in the commercial chain. The course will include tips on how to understand FDA's thinking, negotiate with the FDA and offer anecdotal examples of FDA's import program curiosities.
  • 4 Request Info

    Webinar On Mobile Medical Apps (Is It a FDA Regulated Device?) and Cybersecurity

    With mobile platforms more user friendly, and with computers, tablets and smart phones becoming more powerful, we see an increase in the offering of apps. Some of these apps are specifically targeted to assist individuals in the management of their health and wellness, while other apps are targeted to healthcare providers as tools to assist in the delivery of care.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-MEDICAL-APPS-CYBERSECURITY-509085/AUGUST-2017-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar On C-TPAT Annual Security Training

    The Customs Trade Partnership Against Terrorism is one of the most important trade partnership programs offered to the US trade community in the last 15 years. Benefits associated with membership include expedited customs clearance and mitigation to possible CBP fines and penalties for acts of common compliance error which is now greatly enforced since the passage of the Trade Facilitation and Trade Enforcement Act of 2016.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link
  • 6 Request Info

    Data Integrity FDA/EU Requirements and Implementation 2017

    There is no doubt that data integrity is the current and future inspection focus of all regulatory health care agencies. More than 50% inspection reports such as 483's and Warning Letters quote data integrity as deviations from GxP regulations. This new two-day course provides the regulatory background and guides attendees through the complete record lifecycle from data entry or acquisition through evaluation, reporting, archiving and retrieval. It also helps to fully understand not only the text but also the meaning of related regulations such as FDA's Part 11 and the EU/PICS Annex 11. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901060SEMINAR?trainingregistry-September-2017-SEO
  • 7 Request Info

    Writing and implementing effective SOP 2017

    An SOP is a meticulous step-by-step description of how to do a task that leave no chance for errors and divergence. Writing a good SOP is not an easy job. It requires a firm understanding of the task to be described, an ability to describe in specific unique to that laboratory. Writing, implementing, maintaining and assessing, revising an SOP are all different and necessary jobs. Many people must continuously be involved in these steps. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901140SEMINAR?trainingregistry-September-2017-SEO
  • 8 Request Info

    Webinar On Third Party Vendor Risk Assessment for Financial Firms - Rules, Regulations and Best Practices

    This training program will examine who are third party vendors and analyze why it is critical to prepare a risk assessment for third parties. The course will also offer an overview of the potential risks a third party vendor may impose on your firm.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/RULES-THIRD-PARTY-VENDOR-RISK-ASSESSMENT-FINANCIAL-FIRMS-506445/JULY-2017-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On HIPAA, Ransomware & Cyber Criminal Chaos Prevent, Prepare, Respond and Recover

    Healthcare is the biggest target for Ransomware attacks in 2017. New types of Ransomware are particularly dangerous. They not only lock up your information system - they steal Protected Health Information (PHI).Covered Entities and Business Associates of all types and sizes are prime Ransomware targets because disruption of healthcare operations, even for a brief period, can result in catastrophic harm to patients.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/HIPPA-RANSOMWARE-CYBER-CRIMINAL-504454/JULY-2017-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On Risk-Based Audit Methodology: How to Achieve Enterprise Security

    Attend this training to discover how using a risk-based audit methodology can achieve better enterprise security. Learn how to develop an internal IT audit program, implement risk mitigation methods and develop controls and ensure they are effective.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/RISK-BASED-AUDIT-METHODOLOGY-504012/JULY-2017-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On Three Key Risk Assessments in Your ERM Program - ERM, IT and Internal Controls

    Obtain a better understanding on how to create/develop risk assessments by attending this webinar. The webinar will also help you learn in-depth how to complete the ERM Risk Assessment using the ERM Risk Assessment Matrix and how to complete the general IT Risk Assessment as well as a thorough Risk Assessment for your Internal 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/RISK-ASSESSMENTS-ERM-PROGRAM-509838/JULY-2017-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On CE Mark - Required to Sell Medical Devices in the EU

    This interactive webinar will address the circumstances that regulate medical device sales in the EU. Use of the CE Mark for medical devices is required for selling medical devices in the EU. The webinar will address the use of CE Marking and cover the process of marking which provides an indication of whether the product is in compliance with EU regulations to further allow product commercialization throughout the EU.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/CE-MARK-SELL-MEDICAL-DEVICES-EU-508084/JUNE-2017-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Dos & Don'ts Related to Information Security and Data Privacy

    This training program will prepare your organization to understand the need for data security, the steps that can be taken to institute or augment your data security policies/procedures, and the implementation of the needed controls. This webinar will introduce attendees to a set of known and respected data security standards that can be employed by your organization to improve your security. Attendees will walk away with ideas to leverage the curriculum with their existing security infrastructure.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/DOs-DOnts-INFORMATION-SECURITY-DATA-PRIVACY-505222/JUNE-2017-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Understanding Cyber Insurance Coverage and Leveraging It

    Cyber security is a major risk to any businesses. Threats from thieves and foreign governments or terrorists are constant and ever-evolving. Every day there is a new data breach or threat. In already difficult economic times, managing this risk should be a paramount concern to companies as they strive to remain successful. One way to manage such risk is through insurance.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/CYBER-INSURANCE-COVERAGE-LEVERAGING-502677/JUNE-2017-ES-TRAININGREGISTRY
  • 15 Request Info

    Introduction to Risk Management and Quality System Integration 2017

    Gaps and/or 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 the steps necessary 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 of a device, the 'Safety Case' or 'Assurance Case' document is a well-established method to collect all safety related information together in one place. This documentation will most likely become mandatory for all devices (currently onl
  • 16 Request Info

    Understanding Compliance Program Requirements -HIPAA 2017

    Being in compliance with HIPAA involves not only ensuring that you provide the appropriate patient rights and controls on your uses and disclosures of Protected Health Information; but that you also have the proper policies and procedures in place. If audited or the subject of a compliance review, you will be required to show the government you have all the necessary documentation in place for safeguarding patient Protected Health Information and indicate how you addressed all required security safeguards. This starts with the fundamentals of a HIPAA compliance program. If your healthcare practice, business, or organization needs to understand how to put a HIPAA compliance program in place or make sure the current program is adequate and can withstand government scrutiny, please join us for this informative and interactive two-day training course.
  • 17 Request Info

    Webinar On How to Conduct a Cyber-security Risks Assessment: Are You Prepared?

    Cyber security risks are growing and; knowledgeable financial executives are key to protecting your business from this potential menace. Is your business prepared? All businesses that store customer and corporate confidential data are at risk for hacker attacks. Hackers are well organized and well funded; making defending against these attacks a real challenge. If your business relies on outsourced vendors to help, you need to be sure they are also securing your critical data.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/CYBER-SECURITY-RISKS-ASSESSMENT-503019/JUNE-2017-ES-TRAININGREGISTRY
  • 18 Request Info

    Learn how to streamline your payroll processing procedures for maximum efficiency 2017

    This course covers a very broad range of topics from worker classification, to employee classification, to establishing methods and rates of pay, what must be included in the rate of pay, hours that must be compensated as worked time, required benefits, de minimus working fringes, withholdings and deductions from pay, voluntary deductions, child support and garnishment orders, payroll reporting, analysis of risks of noncompliance, proper documentation of your policies and procedures and record retention requirements. We will show where to find the laws, how to interpret them and how to apply them in the most effective ways.
  • 19 Request Info

    Webinar On Document Retention and Destruction What Human Resource Professionals Must Know

    The only constant thing today is change and with regards to document retention and privacy, laws, regulations are changing all of the time. You need to be diligent to know how, and if, current policy is affected by these changes. To manage an effective program in a cost-effective manner, compliance professionals must rely on information from a broad range of resources within the organization. Records management is the point of convergence of these resources, which is why effective and reliable records management must be part of your Compliance Program.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/DOCUMENT-RETENTION-DESTRUCTION-505871/MAY-2017-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Integrating COBIT with COSO and Other Frameworks

    This webinar addresses the incorporation of Control Objectives for Information and related Technology (COBIT) with other accepted frameworks to ensure aligned information technology and business processes with the organization's adopted frameworks. This presentation also addresses how manager-leaders can affect enterprise governance of IT practices through concepts addressing accountability, roles, interactions, activities and resource use.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/COBIT-COSO-FRAMEWORKS-504757/MAY-2017-ES-TRAININGREGISTRY