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  • 1 Request Info

    Seminar on HIPAA 2019 | HIPAA Security Risk Assessment | What's new?

    This two-day seminar will get into the fine details of what we need to do and how to do it. We will go point by point through the entire HIPAA Security Rule and uncover simple methods to comply and create policy. 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 It will also address major changes under the Omnibus Rule and any other applicable updates for 2018. More: https://www.globalcompliancepanel.com/seminar/HIPAA-2019-What's-new-901951SEMINAR/?SEO
  • 2 Request Info

    Seminar on Phase I GMPs | Drug Development Course

    Early clinical trials are conducted to establish initial safety of a drug. The studies are generally in small number of healthy subjects and use lower doses of the drug product. Therefore, only small amounts of investigational material are required. In order to not undertake substantial costs and to reduce regulatory burden during these early stages, the FDA has established guidelines to allow early stage investigational products to be manufactured under less stringent GMPs. More: https://www.globalcompliancepanel.com/seminar/seminar-on-phase-I-GMPs-901939SEMINAR/?SEO
  • 3 Request Info

    Seminar on Phase I GMPs

    Early clinical trials are conducted to establish initial safety of a drug. The studies are generally in small number of healthy subjects and use lower doses of the drug product. Therefore, only small amounts of investigational material are required. In order to not undertake substantial costs and to reduce regulatory burden during these early stages, the FDA has established guidelines to allow early stage investigational products to be manufactured under less stringent GMPs. More: https://www.globalcompliancepanel.com/seminar/seminar-on-phase-I-GMPs-901939SEMINAR/?SEO
  • 4 Request Info

    Tougher Import Rules for FDA Imports in 2019

    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. More: https://www.globalcompliancepanel.com/seminar/tougher-import-rules-for-FDA-imports-in-2019-901948SEMINAR/?SEO
  • 5 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
  • 6 Request Info

    Seminar on Biostatistics for the Non-Statistician

    Why should you attend: Statistics is a useful decision making tool in the clinical research arena. When working in a field where a p-value can determine the next steps on development of a drug or procedure, it is imperative that decision makers understand the theory and application of statistics. Many statistical softwares are now available to professionals. However, these softwares were developed for statisticians and can often be daunting to non-statisticians. How do you know if you are pressing the right key, let alone performing the best test? More Information Click Here: https://www.globalcompliancepanel.com/seminar/biostatistics-for-the-non-statistician-901936SEMINAR/?SEO
  • 7 Request Info

    How Asperger Syndrome-High Functioning Autism Impact Theory of Mind and Emotional Intelligence

    This presentation will provide participants with a full understanding of the Theory of Mind and how it relates to Asperger Syndrome/High Functioning Autism. This concept can help explain why many individuals with this diagnosis act the way they do. Participants will learn of Baron-Cohen's attempt at assessing the Theory of Mind through the "Sally-Anne Test" and why this testing technique often creates a false negative allowing one to assume the skill is present when in reality it isn't. You will understand why this test doesn't provide the necessary information needed to address the core social deficits of this population. You will learn how perspective taking is a fundamental concern when treating Asperger Syndrome/High Functioning Autism. Participants will be provided with the latest research in Theory of Mind as it relates to how individuals with this diagnosis think and believe.
  • 8 Request Info

    Ten Best Strategies to Treat Worry and Generalized Anxiety Disorder

    Overview: Nearly everyone worries, over 25% of people believe they worry too much, and about 6% of people will suffer from generalized anxiety disorder (GAD). GAD is particularly important to treat as frequently leads to depression, medical problems, and more distressing anxiety disorders like panic disorder and OCD. In this webinar learn why your efforts to manage anxiety and worry have likely failed and learn the 10 best evidence-based treatment strategies to effectively manage GAD. Why should you Attend: Until the mid 90's worry was very difficult to treat and most therapists still struggle with helping clients to manage their worry, anxiety, and depression. Therapists' and individuals' pitfalls of treatment are two-fold: 1) Fighting anxiety actually fuels anxiety and 2) Failure to address the anxiety spiral such that we wait until too late into the anxiety spiral to use coping strategies.
  • 9 Request Info

    How to Best Manage the Emotional Rollercoaster of Asperger Syndrome-High Functioning Autism

    Many professionals are frequently frustrated when presented with a client who has social deficits associated with Asperger Syndrome/High Functioning Autism. These individuals often manifest a variety of deficits that are typically beyond the scope of many well-intentioned therapists. Techniques that have been successfully used for years with clients who struggle with similar issues but do not have the Asperger Syndrome/High Functioning Autism are often ineffective when dealing with this population and leave both the client and professional frustrated. Frequently these clients develop significant stress due to faulty social-pragmatic communication. It is this stress that creates the subsequent behavioral issues resulting in emotional outbursts that many professionals find extremely difficult to manage.
  • 10 Request Info

    Documentation Challenges in Behavioral Health

    This webinar will provide participants with an overview and in-depth examination of compelling documentation issues in behavioral health. Dr. Frederic Reamer will explore high-risk ethical issues and practical strategies designed to protect clients and practitioners. The webinar will explore a series of documentation challenges and explore practical steps that professionals can take to manage ethical issues skillfully and minimize risk. Key topics will include: The content of documentation Documentation wording Credibility issues related to documentation Accessing confidential records Record retention Responding to subpoenas Managing records in integrated health settings
  • 11 Request Info

    Tougher Import Rules for FDA Imports in 2018

    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. Click to Continue Reading: https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901402SEMINAR?trainingregistry-April-2018-SEO
  • 12 Request Info

    HIPAA Training for the Compliance Officer 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. Click to Continue Reading: https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901510SEMINAR?trainingregistry-April-2018-SEO
  • 13 Request Info

    FDA Import Process | FDA Food Facility Registration 2018

    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. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901399SEMINAR?trainingregistry-February-2018-SEO
  • 14 Request Info

    Importance of Dissolution Testing | Plasma Levels of Drug 2018

    Drug dissolution testing is an essential and critical step for appropriate and efficient product development such as tablet and capsule. A number of approaches are used to conduct dissolution testing using different apparatuses and methods. Making a choice for an appropriate apparatus and method has always been confusing and challenging. This seminar will provide relevant pharmacokinetics and physiological background so that making this choice becomes easier and instinctive. No prior knowledge of pharmacokinetic and/or physiology is required; however, these will be explained in very simple terms to help attendees in selecting or developing a dissolution method. This seminar will describe in detail the theoretical aspect of the drug dissolution testing including method development. Pros and cons of different approaches will be explained in detail. Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901495SEMINAR?trainingregistry-February-2018-SEO
  • 15 Request Info

    Enhancing Employee Engagement: Beating Burnout

    Persons who are responsible for the wellness of other persons and systems, such as care providers, managers, customer service staff and administrative professionals, often face stress and burnout resulting in absenteeism, turnover, increased errors and even mortality. This can be very harmful to organizational productivity and credibility, creating costly gaps in care and services. But who cares for the care providers and other employees? Providers and professionals working in education, healthcare, sales and hospitality must be reminded how to assert themselves, set healthy boundaries and respond to stress in healthy ways. Focus groups held by HCEI across the US confirm the need to celebrate the spirit and journey of caring persons while teaching self-preservation skills for the future. When employees care for themselves first they then provide better care and services to others.
  • 16 Request Info

    Celebrating Ourselves: Beating Burnout

    Who cares for the care provider? Both paid and non-paid persons who offer their compassion, skills and resources to those in need are often at risk for burnout, compassion fatigue or vicarious traumatization, creating costly health and emotional challenges and also gaps in expertise and caring. Care providers must be reminded how to assert themselves, set healthy boundaries and respond to stress in healthy ways. Focus groups held by HCEI across the US confirm the need to celebrate the spirit and journey of caring persons while teaching self-preservation skills for the future. When caring persons care for themselves they provide better care for others. Seminar participants will be able to: Understand dynamics of providing care Articulate how each person experiences stress uniquely Identify symptoms of compassion fatigue Utilize practical, proven solutions and exercises for stress reduction Set healthy goals and create a future response plan for stress.
  • 17 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.
  • 18 Request Info

    Combination Products 2017

    This seminar provides Professionals working in this area with A thorough understanding of the complexities involved All the relevant regulations and guidelines Real life examples of how to register and maintain various types of combination products Interfaces: Change Management and LCM Compliant safety reporting for combination products Documentation requirements and interfacing Read More : http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901066SEMINAR?trainingregistry-September-2017-SEO
  • 19 Request Info

    HIPAA Compliance for Small Healthcare Providers 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 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=901024SEMINAR?trainingregistry-September-2017-SEO
  • 20 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