Health and Medicine

Training Options Duration: 90 Minutes Monday, February 26, 2018 | 10:00 AM PST | 01:00 PM EST Overview: OSHA has implemented a new online OSHA 300 Log Recordkeeping Reporting Requirement starting in June 2017. This has created a lot of questions and concerns from companies about what this requirement means and what OSHA will do with this information. Why should you Attend: This course will give a comprehensive overview of what the new OSHA 300 Log Recordkeeping Reporting Requirements are so that a beginner or a seasoned EHS Professional will have confidence in knowing how to fill these out quickly…

Training Options Duration: 90 Minutes Monday, February 26, 2018 | 10:00 AM PST | 01:00 PM EST Overview: OSHA has implemented a new online OSHA 300 Log Recordkeeping Reporting Requirement starting in June 2017. This has created a lot of questions and concerns from companies about what this requirement means and what OSHA will do with this information. Why should you Attend: This course will give a comprehensive overview of what the new OSHA 300 Log Recordkeeping Reporting Requirements are so that a beginner or a seasoned EHS Professional will have confidence in knowing how to fill these out quickly…

Training Options Duration: 90 Minutes Monday, February 26, 2018 | 10:00 AM PST | 01:00 PM EST Overview: This session will focus on the rights of individuals to communicate in the manner they desire, and how a medical office can decide what is an acceptable process for communications with individuals. The session will explain how to discuss communications options with individuals so that you can best meet their needs and desires, while preserving their rights under the rules. With the new HIPAA random audit program now getting under way, and increases in enforcement actions following breaches, now is the time…

This CME-certified live program will help you address diabetes management in patient populations at high risk for diabetes and adverse diabetes-related health outcomes. CCO is partnering with the American Association of Diabetes Educators and the Healthy Trucking Association of America to host 3 live continuing medical education meetings focusing on long haul truck drivers, a population at high risk for diabetes and adverse diabetes-related health outcomes. The first Saturday morning seminar will be held in Atlanta (Feb 24). This interactive seminar is CME-certified for 3.25 credits, and the target audience includes physicians (particularly DOT-certified physicians), physician assistants, and nurse practitioners.…

Il corso si prefigge di fornire indicazioni aggiornate e complete in tema di cardiotocografia partendo dalla patofisiologia degli elementi che caratterizzano il tracciato fino alla gestione clinica delle anomalie che lo caratterizzano. Verranno esplicitate sia le procedure per la cosiddetta "rianimazione in utero" cioè il trattamento conservativo delle anomalie cardiotocografiche che quelle relative alle emergenze cardiotocografiche che prevedono la più rapida sottrazione del feto al rischio di acidosi. Chiarezza verrà fatta in tema di classificazioni del tracciato cardiotocografico, sia confrontando le peculiarità delle diverse linee guida internazionali attualmente in uso, sia esponendo la recente classificazione italiana nata sotto l’egida della…

Students learn field herbal medicine for remote & off-grid situations of illness or injury with hands-on experience using clinical and role-playing based training in post-disaster scenarios. Winter Wilderness Emergency First Aid Certification Training. Students will learn an emphasis on field herbal medicine that can be realistically used in remote and off-grid situations of illness or injury with hands-on experience using clinical and role-playing based training in post-disaster scenarios. This is a 24 hour course taught over 3 days (8 hours per day) and includes both a conventional 16-Hour Wilderness First Aid (WFA) Certification through Emergency Care and Safety Institute (ECSI)…

Short Description : The two day workshop on GMP for Quality Control Laboratories and FDA Audit Preparation, is designed to provide an in-depth understanding of the regulatory background and guides attendees through all critical areas of GMP compliance. You will gather a thorough awareness of latest trends and updates with respect to USFDA, EU, WHO and PIC/S (Pharmaceutical Inspection Co-operation Scheme) and Indian GLP Schedule L1 compliance and guideline requirements. This course will also provide examples to develop inspection ready documentation. Full description : On completion of this course, the participants shall be well versed with the global Quality control…

The impact of Data Integrity issues on a regulated company can be significant: it can result in recalls of products, warning or untitled letters, import alerts, injunctions, seizures, legal action, etc. These regulatory actions can have significant financial impact to the company. However, and most importantly, data integrity issues can lead to potential patient harm!! Defined by the Medicines and Healthcare Products Regulatory Agency (MHRA) as "the extent which all data are complete, consistent and accurate throughout the data lifecycle", data integrity is increasingly the focus of regulatory agencies round the world. Companies must now ensure that they are appropriately…

This seminar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program. The ISO 62366 is an "Consensus" Standard, making it a gold standard for regulatory submissions. We will look at other reference points regarding HF, like AAMI/ANSI HE75:2009 and how HF Engineering include consideration of: Device Users Use Environments and User Interfaces Preliminary Analyses Exploratory HF/Usability Evaluations Hazard Mitigation and Control We will look at the implication of HFE through Design Controls in the QSR: Design input -includes "needs of the user and patient" Design…

Why should you attend: Good clinical data management (CDM) is paramount for a successful research. After all, Garbage In, Garbage Out (GIGO). CDM is involved in all aspects of collecting, processing, and interpreting information. There are many types of computer applications and database systems to support data collection and management. However, there are elements of Good Clinical Practice that apply across the board. Review and approval of drugs or devices by regulatory agencies requires the assumption that the data presented are valid and reliable. Integrity of the data is paramount to ensure confidence in the results and conclusions you will…

Training Options Duration: 60 Minutes Thursday, February 22, 2018 | 10:00 AM PST | 01:00 PM EST Overview: In 2013, The US Department of Health and Human Services made major changes to rules implementing The Health Insurance and Portability Act of 1996 (HIPAA) and Health Information Technology for Economic and Clinical Health Act of 2003 (HITECH). Among the many areas impacted by these rules (billing, marketing, research, IT security, etc.) is fund raising. The amendments significantly modify the methods and practice that hospitals, their institutionally related foundations, and other healthcare charities may or must employ when using ANY patient or…

Training Options Duration: 60 Minutes Wednesday, February 21, 2018 | 10:00 AM PST | 01:00 PM EST Overview: Being in compliance with HIPAA involves not only ensuring you provide the appropriate patient rights and controls on your uses and disclosures of protected health information, but you also have the proper policies and procedures in place. A HIPAA Risk Management plan is your overall policies and procedures manual. If audited or the subject of a compliance review you will be required to show the government you have all the necessary policy and procedure documentation in place to address all the required…

OVERVIEW This HIPAA & Privacy Act Training covers confidentiality beyond the privacy and other protections required by HIPAA. An in-depth overview of medical records keeping starts this webinar examining the state law sources and even contractual requirements of medical record keeping. The webinar proceeds to review exceptions to confidentiality that is most frequently encountered by mental health professionals who practice in a high-risk setting where the consequences of a misstep can be very high. For many years now, HIPAA has provided a federal right to privacy for patient medical records, including mental health records. However, fearing issues not with federal…

OVERVIEW This webinar will provide an in-depth understanding of the Federal False Claims Act, Federal Anti-Kickback and Stark laws, and discuss how marketing activities can trigger either or both. WHY SHOULD YOU ATTEND This webinar will provide the basic building blocks you will need to develop and maintain your company’s precious commodity – your reputation – and eliminate exposure to fraud charges based on marketing practices. It will also cover the practical requirements and operations, principles of compliance and the basic elements that every business has to have to reduce civil and criminal liabilities and economic sanctions. AREAS COVERED •…

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. Each stage of project management - Initiate, Planning, Executing, Monitoring and Controlling and Closing will be detailed. Activities highlighting each step of the process and key concept will be presented…

Un hackathon 100% Blockchain, pour faire du groupe Casino un des premiers aexploiter la blockchain dans le secteur de la grande distribution en France. Votre mission Rendre la traçabilitE des produits et des transactions infaillibleFaire en sorte que l'identitE de chaque acteur de la supply chain (Eleveur, abattoirs, transformateurs, centres logistiques, distribution, retail) ainsi que les informations concernant chaque transaction soient enregistrEes sur un systeme de blockchain. Fiabiliser les transactions via un systeme de blockchainTracer toutes les Etapes de vente sur une marketplace. Faciliter les paiements via une carte de fidElitE. REvolutionner les systemes de fidElisation. Les prix 1er :…

Background: 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…

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. Additionally, the seminar will cover the impending changes coming with the EU Parliament passage of the EU Clinical Trial Regulation, which will affect…

The 2-day seminar explains how to apply statistics to manage risks and verify/validate processes in R&D, QA/QC, and Manufacturing, with examples derived mainly from the medical device design/manufacturing industry. The flow of topics over the 2 days is as follows: ISO standards and FDA/MDD regulations regarding the use of statistics. Basic vocabulary and concepts, including distributions such as binomial, hypergeometric, and Normal, and transformations into Normality. Statistical Process Control Statistical methods for Design Verification Statistical methods for Product/Process Qualification Metrology: the statistical analysis of measurement uncertainty, and how it is used to establish QC specifications How to craft "statistically valid…

Training Options Duration: 60 Minutes Tuesday, February 13, 2018 | 10:00 AM PST | 01:00 PM EST Overview: Hospitals must file a National Practitioner Data Bank report on any physician’s surrender of privileges if an investigation is underway. This has always been a Data Bank reporting requirement, intended to discourage plea bargains which allowed physicians to avoid being reported if they agreed to waive hearing rights. Under the new Guidebook, expanded descriptions of "investigation" and "surrender" stretch what is to be considered a reportable surrender of privileges. OPPE and FPPE and other peer review can be affected, as are physicians’…