Health and Medicinerss


GRIT for Women in Medicine:  Growth, Resilience, Inspiration, and Tenacity

GRIT for Women in Medicine: Growth, Resilience, Inspiration, and Tenacity

Location: , United States
Category: Health and Medicine
Start Date: 09-20-2017 Last Day: 09-22-2017
Description: This course will empower women and men in medicine with the skills and resources to remove barriers and bias of women in leadership positions specific to the challenges in healthcare. Leaders in business and healthcare will present evidence-based strategies to promote professional development and enhance personal well-being. Nationally, there is large number of female clinicians reporting burnout which has a potential effect on patient experience, compliance, and outcomes. This course will address the growing need for improved clinician wellness and development for a gender balanced leadership healthcare team. Audience: This course is intended for professional women and men in…
Allgemeinmedizin- Refresher

Allgemeinmedizin- Refresher

Location: , Germany
Category: Health and Medicine
Start Date: 01-24-2018 Last Day: 01-27-2018
Der Allgemeinmedizin Refresher findet vom 24. - 27. Januar 2018 in Frankfurt statt. Mit über 5.000 teilnehmenden Ärzten zählen unsere Fortbildungen im Bereich Allgemeinmedizin und Innere Medizin zu den beliebtesten Kursen im deutschsprachigen Raum. In kurzen, 30 – 40 minütigen Blöcken werden die neuesten diagnostischen und therapeutischen Leitlinien der Allgemeinmedizin von Spezialisten präsentiert und auf Ihre Fragen eingegangen. Dabei wird vor allem auf Praxisrelevanz und Didaktik großen Wert gelegt. Unsere Referenten sind Experten in ihren Fachbereichen mit langjähriger Erfahrung in ihrem Betätigungsfeld. Sie kommen aus renommierte Einrichtungen wie zum Beispiel aus dem Universitätsklinikum Frankfurt, dem Agaplesion Markus Krankenhaus Frankfurt oder…
Statistical Process Control & Process Capability

Statistical Process Control & Process Capability

Location: , United States
Category: Health and Medicine
Start Date: 02-01-2018 Last Day: 02-02-2018 Deadline for abstracts: 02-01-2018
This course teaches participants the fundamental concepts and methods needed to establish effective control charts and estimate process capability. In addition to learning traditional control charts (e.g. xbar, r/s), participants will be exposed to other useful charts for handling multiple sources of variation (within/between) and short production runs. Practical aspects of implementing SPC on the shop floor are also discussed. Estimating process capability for both normal and non-normal data is discussed. The meaning and limitations of popular capability are presented in detail. This highly interactive course will allow participants the opportunity to practice applying SPC techniques with various data sets.…
Webinar On 2018 CPT and HCPCS Updates

Webinar On 2018 CPT and HCPCS Updates

Location: , United States
Category: Health and Medicine
Start Date: 02-06-2018 Last Day: 02-06-2018 Deadline for abstracts: 02-05-2018
Training Options Duration: 60 Minutes Tuesday, February 6, 2018 | 10:00 AM PST | 01:00 PM EST Overview: 2018 will see significant changes in each section of the CPT and HCPCS manuals. There have been over 350 code changes with the update. This hour-long presentation will navigate you through the changes per each chapter of the CPT and HCPCS manuals. This webinar will also provide the tools necessary to remain compliant and continue the revenue cycle process day one of go-live. Why should you Attend: Coders today use HCPCS codes to represent medical procedures to Medicare, Medicaid and several other…
Medical Device Registration and Approval Process for the Pacific Rim (including India, Japan, China, Singapore, Australia, Taiwan, Hong Kong, and other locations)

Medical Device Registration and Approval Process for the Pacific Rim (including India, Japan, China, Singapore, Australia, Taiwan, Hong Kong, and other locations)

Location: , Switzerland
Category: Health and Medicine
Start Date: 02-07-2018 Last Day: 02-08-2018 Deadline for abstracts: 02-06-2018
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…
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan

Location: , United States
Category: Health and Medicine
Start Date: 02-08-2018 Last Day: 02-09-2018 Deadline for abstracts: 02-06-2018
Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable. One such example is the Medical Device Single Audit Program [MDSAP], where Authorized Organizations would be allowed to carry out a single GMP audit on medical device manufacturing facilities and have it…
Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans

Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans

Location: , United States
Category: Health and Medicine
Start Date: 02-08-2018 Last Day: 02-09-2018 Deadline for abstracts: 02-07-2018
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…
HIPAA Training for the Compliance Officer

HIPAA Training for the Compliance Officer

Location: , United States
Category: Health and Medicine
Start Date: 02-08-2018 Last Day: 02-09-2018 Deadline for abstracts: 02-07-2018
This lesson will be addressing how practice/business managers (or compliance officers) 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…
HR Auditing: Identifying and Managing Key Risks

HR Auditing: Identifying and Managing Key Risks

Location: , United States
Category: Health and Medicine
Start Date: 02-12-2018 Last Day: 02-13-2018 Deadline for abstracts: 02-11-2018
HR audits are designed to help your organization focus its attention on its human resource management practices, policies, procedures, processes, and outcomes by providing you with a structured and systematic series of questions about key compliance, risk management, internal auditing, and human resource management issues. As a process, HR audits are designed to help your organization identify potential and actual problem areas, help assess the effectiveness of current HR management activities, help assess weaknesses in HR internal control processes, and help assess human capital strategic and compliance related risks. HR audits should additionally provide suggestions for corrective action. Importantly, HR…
Webinar On National Practitioner Data Bank Expanded Reporting Parameters

Webinar On National Practitioner Data Bank Expanded Reporting Parameters

Location: , United States
Category: Health and Medicine
Start Date: 02-13-2018 Last Day: 02-13-2018 Deadline for abstracts: 02-12-2018
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’…
The EU Clinical Trial Regulation + EU Filings & Registrations

The EU Clinical Trial Regulation + EU Filings & Registrations

Location: , Switzerland
Category: Health and Medicine
Start Date: 02-14-2018 Last Day: 02-15-2018 Deadline for abstracts: 02-13-2018
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…
Applied Statistics, with Emphasis on Verification, Validation, Sample Size, and Risk Management, in R&D, Manufacturing, and QA/QC

Applied Statistics, with Emphasis on Verification, Validation, Sample Size, and Risk Management, in R&D, Manufacturing, and QA/QC

Location: , United States
Category: Health and Medicine
Start Date: 02-14-2018 Last Day: 02-15-2018 Deadline for abstracts: 02-13-2018
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…
Tougher Import Rules for FDA Imports in 2018

Tougher Import Rules for FDA Imports in 2018

Location: , United States
Category: Health and Medicine
Start Date: 02-15-2018 Last Day: 02-16-2018 Deadline for abstracts: 02-13-2018
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…
Blockchain And Shop hackathon

Blockchain And Shop hackathon

Location: , France
Category: Health and Medicine
Start Date: 02-16-2018 Last Day: 02-18-2018
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 :…
Project Management for Non-Project Managers

Project Management for Non-Project Managers

Location: , United States
Category: Health and Medicine
Start Date: 02-20-2018 Last Day: 02-21-2018 Deadline for abstracts: 02-19-2018
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…
Developing HIPAA Policies and Procedures Webinar 2018

Developing HIPAA Policies and Procedures Webinar 2018

Location: , United States
Category: Health and Medicine
Start Date: 02-21-2018 Last Day: 02-21-2018 Deadline for abstracts: 02-20-2018
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…
HIPAA & Privacy Act Training

HIPAA & Privacy Act Training

Location: , United States
Category: Health and Medicine
Start Date: 02-21-2018 Last Day: 02-21-2018 Deadline for abstracts: 02-21-2018
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…
Stark Law Training by William Mack Copeland

Stark Law Training by William Mack Copeland

Location: , United States
Category: Health and Medicine
Start Date: 02-21-2018 Last Day: 02-21-2018 Deadline for abstracts: 02-21-2018
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 •…
GMP for Quality Control Laboratories and FDA Audit Preparation

GMP for Quality Control Laboratories and FDA Audit Preparation

Location: , India
Category: Health and Medicine
Start Date: 02-22-2018 Last Day: 02-23-2018 Deadline for abstracts: 02-21-2018
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…
A Risk Based Approach To Data Integrity

A Risk Based Approach To Data Integrity

Location: , United States
Category: Health and Medicine
Start Date: 02-22-2018 Last Day: 02-23-2018 Deadline for abstracts: 02-20-2018
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…

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