Teaching & Instruction

If you can't find what you want, Ask Us.

Refine Your Results

Location

Dates

FEATURED VENDORS

Showing 21-40 of 43 results Sort by:

Courses

  • 21 Request Info

    Supplier Management for Medical Device Manufacturers 2017

    Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901162SEMINAR?trainingregistry-November-2017-SEO
  • 22 Request Info

    21 CFR Part 11 Compliance for Computer Systems Regulated by FDA 2017

    The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philosophy and approach, and incorporating it into the overall computer system validation program and plans for individual systems that have this capability. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901297SEMINAR?trainingregistry-November-2017-SEO
  • 23 Request Info

    Project Management for Non-Project Managers

    This two-day seminar will begin by laying the foundation for the subject by first defining what a project is and then discussing the unique roles that the project manager must assume along the length of any project. The Triple Constraint, the most fundamental of project management principles, will be explained in detail with examples and tools provided that can be used to integrate the principle into any project management process. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900998SEMINAR?trainingregistry-November-2017-SEO
  • 24 Request Info

    GMP and Regulatory Expectations for Early IND Products 2017

    This course will present, in one place, the regulations and guidelines that apply to early phase products. In some cases these will not be regulations, but needs that, if met, will increase the efficiency of activities as a product proceeds through the development process. The course will present these items in the order of product development from the point of R & D activities to the completion of Phase 2 clinical trials. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901318SEMINAR?trainingregistry-November-2017-SEO
  • 25 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 Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900992SEMINAR?trainingregistry-November-2017-SEO
  • 26 Request Info

    Onsite GCP Review and Update including the all-important 'Investigators Responsibility' 2017

    Engineers are dedicated to making things work, so a focus on how they might fail and harm someone can seem alien. Managing risk, however, is essential for all medical products- medical devices, including those involving software, have produced some painful examples of poor risk management with serious consequences. Experience has shown that there is a better way, that it is possible to manage risk in a changing business and technical world. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901348SEMINAR?trainingregistry-November-2017-SEO
  • 27 Request Info

    The EU Clinical Trial Regulation + EU Filings & Registrations 2017

    This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Directive and the impending changes coming to the EU through the EU Clinical Trial Regulation (for Drugs, Biologics & Combination Products). The course also covers recent updates on EU-GCP associated with the new regulatory framework, the highlights of the new EU Pharmacovigilance Directive, as it relates to studies and helpful tips into working with the European regulators. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901354SEMINAR?trainingregistry-November-2017-SEO
  • 28 Request Info

    Validation, Verification and Transfer of Analytical Methods from FDA/EMA, USP and ICH 2017

    Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated. Method validation recently got highest attention from regulatory agencies and industry task forces. For example, FDA and EMA released guidelines on method validation and transfer, and USP has proposed new approaches chapters for integrated validation, verification and transfer of analytical procedures, for equivalency testing and for statistical evaluation.
  • 29 Request Info

    The EU General Data Protection Regulation (GDPR) 2017

    On 25th May 2018 the EU-GDPR becomes effective, this date has been set to give organisations time to prepare and comply with the regulations. This may seem to be a long way off, but for most organisations there is a lot to be done. With the escalation of data breaches, the sooner data is safe guarded the better. Often a data breach is not discovered for months, sometimes six months, implementing new policies, security systems, negotiations with suppliers and training people in an organisation will take time. The sooner you start the more time you have to make a good decision on the options you face. This introductory course will give you an overview of the history of Data Protection within the EU and introduce you to the enhancements and new obligations imposed by the EU GDPR Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901168SEMINAR?trainingregistry-September-2017-SEO
  • 30 Request Info

    HIPAA Compliance for Small Healthcare Providers 2017- Before 30 April 50% Discount for its All Seminars

    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 small healthcare practice 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. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901022SEMINAR?trainingregistry_SEO
  • 31 Request Info

    Writing and implementing effective SOP's 2017- Before 30 April 50% Discount for its All Seminars

    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. Even a standardized method, such as an ASTM or IP method, is insufficiently written to pass as a well-written and compliant SOP. The reasons why will be described, as will the steps needed to convert a standard method into an SOP. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900914SEMINAR?trainingregistry_SEO
  • 32 Request Info

    Applied Statistics for Scientists and Engineers 2017- Before 30 April 50% Discount for its All Seminars

    Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting validation criteria and specifications, performing measurement systems analysis (MSA), conducting stability analysis, using design of experiment (DOE) for process development and validation, developing process control charts, and determining process capability indices. Different statistical methods are required for each of these particular applications. Data and tolerance intervals are common tools used for setting acceptance criteria and specifications. Simple linear regression and analysis-of-covariance (ANCOVA) are used for setting expiries and conducting stability analysis studies. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900788SEMINAR?trainingregistry_SEO
  • 33 Request Info

    HIPAA for the Compliance Officer 2017- Before 30 April 50% Discount for its All Seminars

    I will be going into great detail regarding you practice or business and how it relates to the HIPAA Security/Privacy Rule, Areas covered will be history of HIPAA, privacy vs security, business associates, changes for 2016, audit process, paper based PHI, HIPAA and suing, texting, email, encryption, medical messaging, voice data and much, much, more I will uncover myths versus reality as it relates to this very enigmatic law based on over 600 risk assessments performed as well as years of experience in dealing directly with the Office of Civil Rights HIPAA auditors. I will also speak to real life audits conducted by the Federal government (I've been on both sides of these audits) what your highest risks are for being fined (some of the risk factors may surprise you). Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900962SEMINAR?trainingregistry_SEO
  • 34 Request Info

    Master HIPAA Compliance in Six Steps 2017- Before 30 April 50% Discount for its All Seminars

    The secret is - HIPAA Rules are easy and routine to follow - when they are explained step-by-step in plain language. In this seminar Paul Hales will capture your attention with visual presentations, discussion and learning exercises and show how to find the right rule with the step-by-step procedures you need when you need them. Seminar Takeaways: Thorough Understanding of HIPAA Rules What they are How they work together Why and How they were made How they are changing and what to expect next HIPAA Risk Analysis - Risk Management for Your Organization A Practical Guided Exercise done in class on your computer to take home Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900908SEMINAR?trainingregistry-SEO
  • 35 Request Info

    Background Checks, Criminal Records and Safe Hiring 2017 Effective and Compliant Program 2017- Before 30 April 50% Discount for its All Seminars

    Employee problems are caused by problem employees, and this session will help HR professionals legally avoid bad hires in the first place. Just one bad hire can result in a legal and financial nightmare. Without taking appropriate steps, there is a near statistical certainty that an employer will hire someone with an unsuitable criminal record, or a falsified background, that can result in workplace violence, lawsuits for negligent hiring and time wasted recruiting and hiring the wrong person. On the other side of the screening fence, are the rising tides of lawsuits against employers alleging screening methods violate the law or are at odds with changes in civil rights legislation and the new EEOC Guidance on the use of criminal records. The screening landscape is more complex than ever. Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900916SEMINAR?trainingregistry_SEO
  • 36 Request Info

    Training Certificate

    The ATD Training Certificate content is practical and grounded in the real world, not just academic theory. This program focuses on what happens before, during, and after you deliver training, and what to do if training is not the right solution. With input from ATD’s Competency Study, we identified the competencies required by the most successful practitioners. The Training Certificate Program is aligned with the Training Delivery Area of Expertise in the ATD Competency Model. Learner feedback indicates high value in the following areas: student engagement, expert facilitation, and applicable tools and techniques.
  • 37 Request Info

    Security Officer and HIPAA 2017

    This webinar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017. Areas also covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT. The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, there is so much misleading information all over regarding the do's and don'ts with HIPAA - I want to add clarity for compliance officers
  • 38 Request Info

    Webinar On Train the Trainer: Key Tips for Engaging Adult Learners

    Adult learning is defined as ‘the entire range of formal, non-formal and informal learning activities which are undertaken by adults after a break since leaving initial education and training, and which results in the acquisition of new knowledge and skills’. In order for adults to acquire new knowledge and skills, we must deliver training to meet their learning needs. In this course, you will learn about the theories and methods to engage in Adult Learner.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/KEY-TIPS-ENGAGING-ADULT-LEARNERS-501938/DECEMBER-2016-ES-TRAININGREGISTRY
  • 39 Request Info

    Risks of Omission by Compliance4all

    Overview: The risk of omission, or what we don't do right, is usually far more dangerous than the risk of what we do wrong (poor quality). Poor quality generally announces its presence during inspections and tests (internal failure) or, in the worst case, when customers complain about it (external failure). This leads to corrective and preventive action (CAPA) to remove the root causes of the problems in question. The other six Toyota production system wastes are, on the other hand, asymptomatic. They do little or nothing to announce their presence, and can hide in plain view from people who are not trained to recognize them. Henry Ford, Taiichi Ohno, and Shigeo Shingo all described the asymptomatic nature of these wastes.
  • 40 Request Info

    Information from Geochemical Data by Compliance4all

    Overview: Most specialists strongly recommend to sample every meter of the drill core or of a trench and to use multielement analysis, rather than just asking the laboratory for gold test. There are also many other types of analysis that are ignored by the industry. But even when such analyses are requested, most of the time the fed geologist is not well trained on the necessary techniques and methods to extract all the information contained in the data. This webinar will teach you what to ask and how to extract all the important information of your data. Why should you Attend: You, as a person making decisions on where to drill or how to manage your exploration budget, will benefit from this seminar that will show you all types of analyses that can be requested to help you in your exploration goal- finding the new ore body.