Health and Medicinerss


ISO 14971 Risk Management Training-IEC 62304 Risk Management

ISO 14971 Risk Management Training-IEC 62304 Risk Management

Location: , Switzerland
Category: Health and Medicine
Start Date: 03-27-2018 Last Day: 03-28-2018 Deadline for abstracts: 03-26-2018
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…
Key Legal Considerations When Redesigning Your Physician Compensation Plans

Key Legal Considerations When Redesigning Your Physician Compensation Plans

Location: , United States
Category: Health and Medicine
Start Date: 03-28-2018 Last Day: 03-28-2018 Deadline for abstracts: 03-27-2018
Training Options Duration: 60 Minutes Wednesday, March 28, 2018 | 11:00 AM PDT | 02:00 PM EDT Overview: In this session Mr. Wolfe will provide an overview of the Stark Law, including its technical requirements and key tenets of defensibility. He will also discuss best practices for structuring evaluating and structuring new compensation models. The webinar will focus on regulatory requirements, key provisions, valuation considerations and potential pitfalls that should be avoided. Why should you Attend: As health care organizations redesign their compensation plans, they must be sure the process they follow and the models the new models they develop…
Outcome Enhancement of Your Home Health Agency in 2018

Outcome Enhancement of Your Home Health Agency in 2018

Location: , United States
Category: Health and Medicine
Start Date: 03-28-2018 Last Day: 03-28-2018
Product Format: Live Audio Conference Presenter: Melissa Abbott, RN, MSN/MHA Conference Date: Wednesday, March 28, 2018 Aired Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Length: 90 minutes Price: $197.00 Join expert speaker Melissa Abbott, RN, MSN/MHA for an information-packed educational session and learn how to boost your home health agency’s outcome measures in 2018. Melissa will show you how to understand your CASPER reports and Star Ratings by peeling back the layers of jargon to reveal how these reports tie back to real-world home healthcare practices. This session will not only…
FDA Guidelines for Pharmaceutical Industry | FDA Regulatory 2018

FDA Guidelines for Pharmaceutical Industry | FDA Regulatory 2018

Location: , United States
Category: Health and Medicine
Start Date: 03-29-2018 Last Day: 03-30-2018 Deadline for abstracts: 03-27-2018
The FDA is increasing its enforcement actions both for domestic and foreign inspections. Enforcement statistics have not been summarized yet because 2017 has not ended yet. We are certainly seeing more Warning Letters and Import Alerts based on Data Integrity (21 CFR Part 11: Electronic Records; Electronic Signatures. In the past FDA used to issue several Warning Letters to the same firms upon consecutive inspections. Today, after receiving one Warning Letter the next regulatory action is elevated to Import Alert, Consent Decree, and Injunctions for domestic manufacturers. Senior Management must take the initiative in setting the tone of full compliance:…
HIPAA Compliance Requirements | HIPAA Privacy Security 2018

HIPAA Compliance Requirements | HIPAA Privacy Security 2018

Location: , United States
Category: Health and Medicine
Start Date: 03-29-2018 Last Day: 03-30-2018 Deadline for abstracts: 03-27-2018
Being the HIPAA Security and Privacy Official involves not only ensuring you know 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. If audited or the subject of a breach investigation, 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 HIPAA Security and Privacy Official needs to understand what…
European Data Protection Regulation - 2018 Implementation

European Data Protection Regulation - 2018 Implementation

Location: , United States
Category: Health and Medicine
Start Date: 03-29-2018
Overview: 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. Why should you Attend: Attendees will learn the common EU rules that have been established to ensure that personal data has a high standard of protection across the EU. Attendees will also learn about their rights to complain and obtain redress if their data is misused in any of the EU member states. Areas Covered in the Session: How EU Data Protection Regulation affect social networks How EU Data Protection Regulation benefit existing European…
The Dubai International Neuroscience Congress

The Dubai International Neuroscience Congress

Location: , United Arab Emirates
Category: Health and Medicine
Start Date: 03-29-2018 Last Day: 03-31-2018 Deadline for abstracts: 03-29-2018
The Dubai International Neuroscience Congress is designed to cover the latest approaches in Neuroscience and current updates on management and treatment in different areas. Dubai International Neuroscience Congress taking place 29-31 March 2018 in Dubai, UAE. The programme is designed to cover the latest contemporary approaches in Neurology and current updates on management and treatment in different areas; mental disorders, schizophrenia, Alzheimer, bi polar disorders, adult eating disorders, and many more... The congress will feature interactive case-studies, platform presentations, meet the expert sessions, educational workshops, networking sessions and more, to provide a comprehensive review of current issues and recent advances…
Understanding and Implementing an Effective Laboratory Quality Management System

Understanding and Implementing an Effective Laboratory Quality Management System

Location: , United States
Category: Health and Medicine
Start Date: 04-02-2018 Last Day: 04-02-2018 Deadline for abstracts: 04-02-2018
OVERVIEW Part 1 QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025: The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the “what to do” component of a QMS. What is also needed are the “how to do it” or procedures and methods and finally the controls or evidence that it was done properly. This is the 1st of two webinars on…
What you Need to Know as a Healthcare Provider(Patient Rights, Medical Records and HIPAA)

What you Need to Know as a Healthcare Provider(Patient Rights, Medical Records and HIPAA)

Location: , United States
Category: Health and Medicine
Start Date: 04-03-2018 Last Day: 04-03-2018 Deadline for abstracts: 04-02-2018
Training Options Duration: 60 Minutes Tuesday, April 3, 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. 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 privacy safeguards. This starts with the fundamentals…
How to Use and Validate Excel Spreadsheets to Ensure Compliance under FDA’s 21 CFR Part 11

How to Use and Validate Excel Spreadsheets to Ensure Compliance under FDA’s 21 CFR Part 11

Location: , United States
Category: Health and Medicine
Start Date: 04-03-2018 Last Day: 04-03-2018
Product Format: Live Webinar Presenter(s): Dr. David Lim, Ph.D., RAC, ASQ-CQA Conference Date: Tuesday, April 3, 2018 Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Duration: 60 minutes Price: $227.00 Join this session with expert speaker Dr. David Lim and learn how to adequately develop and implement Excel spreadsheet computer system validation in your organization in compliance with FDA’s 21 CFR Part 11. You will get in-depth insights to improve your awareness in order to better implement Part 11 and computer system validation requirements to avoid citations in 483s and warning letters.…
2018 Case Management: Complying with the Conditions of Participation and Other Regulatory Requirements

2018 Case Management: Complying with the Conditions of Participation and Other Regulatory Requirements

Location: , United States
Category: Health and Medicine
Start Date: 04-03-2018 Last Day: 04-03-2018
Product Format: Live Audio Conference Presenter(s): Toni G. Cesta, Ph.D., RN, FAAN Conference Date: Tuesday, April 3, 2018 Aired Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Length: 60 minutes Price: $227.00 In this session, industry veteran Toni G, Cesta will help you understand how to maintain compliance in a variety of areas directly related to utilization management and discharge planning. You’ll learn how to survive Joint Commission and CMS audits that are scrutinizing hospitals’ and case management departments’ compliance with the Conditions of Participation and other regulatory requirements. For Registration, visit…
2nd Clinical Trial Financial Management Summit

2nd Clinical Trial Financial Management Summit

Location: , United States
Category: Health and Medicine
Start Date: 04-04-2018 Last Day: 04-05-2018
ExL Events' 2nd Clinical Trial Financial Management Summit, convening on April 4–5, 2018 in Philadelphia, is designed to provide attendees with innovative solutions that deliver on-budget clinical trials using real-world data. Attendees will learn to manage contracts and negotiations with outsourcing partners and vendors; balance savings, quality, and speed in the selection of CROs and vendors; and pinpoint best practices for funding clinical trials through grants and government. Our fantastic, high level speaking faculty will tackle the all of these challenges and more during this two-day event. URLs: Brochure: https://go.evvnt.com/193735-1?pid=154 Booking: https://go.evvnt.com/193735-2?pid=154 Time: 8:00 am to 5:00 pm Prices: Early…
HIPAA Risk Analysis-Risk Management - Explained & Demonstrated

HIPAA Risk Analysis-Risk Management - Explained & Demonstrated

Location: , United States
Category: Health and Medicine
Start Date: 04-04-2018 Last Day: 04-04-2018 Deadline for abstracts: 04-03-2018
Training Options Duration: 60 Minutes Wednesday, April 4, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: This webinar for HIPAA Covered Entities and Business Associates will explain: What a complete HIPAA Risk Analysis - Risk Management program is and how to do one How to automate, simplify, document and complete your HIPAA Risk Analysis - Risk Management by an interactive, intuitive process: To identify and analyze Risks to all Protected Health Information (PHI) - not just Electronic Protected Health Information (EPHI) Manage Identified Risks Implement your specific, customized Risk Management Plan Archive your Risk Analysis - Risk Management-…
Veterinary Hospital Infect. Control and Antimicrob. Stewardship

Veterinary Hospital Infect. Control and Antimicrob. Stewardship

Location: , United Kingdom
Category: Health and Medicine
Start Date: 04-04-2018 Last Day: 04-04-2018 Deadline for abstracts: 04-04-2018
Challenges in Veterinary Hospital Infection Control and Antimicrobial Stewardship. Course Objectives: The objectives are to promote hospital infection control and antimicrobial stewardship in small animal practice and to educate a new generation of veterinary infectious disease specialists to be able to develop and implement infection control programmes (ICPs) and antimicrobial stewardship programmes (ASPs). Postgraduate education in this area is regarded as one of the key missions of ESGVM in order to meet the current public and animal health concerns related to the occurrence of multidrug-resistant bacteria and the increasing demand for responsible antibiotic use in veterinary medicine. The course will…
Discussion on Raw Material Methods and Specifications

Discussion on Raw Material Methods and Specifications

Location: , United States
Category: Health and Medicine
Start Date: 04-04-2018 Last Day: 04-04-2018 Deadline for abstracts: 04-03-2018
Overview: Based on knowledge of the active and inactive ingredient's function and role in the finished dosage form, Compendia methods and specifications are clearly accepted by third parties and regulatory agencies. Why should you Attend: The FDA has Approved hundreds of inactive ingredients for thousands of products with various dosage forms (routes of administration). The quantities and quality of each inactive ingredient is critical to the function and design of the final product formulation. Areas Covered in the Session: Description of the API and excipient manufacturing process and facility The supplier's commitment to conforming to appropriate excipient GMP requirements Characterization…
Evolution of the Quality Management System - How to go from Surviving to Thriving 2018

Evolution of the Quality Management System - How to go from Surviving to Thriving 2018

Location: , United States
Category: Health and Medicine
Start Date: 04-05-2018 Last Day: 04-06-2018 Deadline for abstracts: 04-04-2018
Course "Evolution of the Quality Management System - How to go from Surviving to Thriving" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Using lecture, discussion, and exercises, this 2 day seminar will focus on taking your QMS from surviving to thriving. We'll move from understanding the regulatory requirements, how to create your QMS structure, process thinking, and developing your improvement strategy. We'll discuss tools and techniques for improvement and how to measure your progress. Why you should attend: Many companies struggle to establish and maintain a…
eCTD Submissions of IND/NDA to the US FDA, EU and Canada 2018

eCTD Submissions of IND/NDA to the US FDA, EU and Canada 2018

Location: , United States
Category: Health and Medicine
Start Date: 04-05-2018 Last Day: 04-06-2018 Deadline for abstracts: 04-03-2018
Course "eCTD Submissions of IND/NDA to the US FDA, EU and Canada" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substantially limited. The CTD has improved the regulatory review processes and enabled implementation of good…
Representations & Warranties in Physician Practice Acquisitions

Representations & Warranties in Physician Practice Acquisitions

Location: , United States
Category: Health and Medicine
Start Date: 04-05-2018 Last Day: 04-05-2018
Product Format: Live Webinar Presenter(s): Steven T. Lawrence, MBA, JD, LLM Conference Date: Thursday, April 5, 2018 Aired Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Length: 60 minutes Price: $227.00 Join this session with healthcare attorney Steven Lawrence, JD, MBA, LLM where he will instruct you on the current state of representations and warranties in physician practice transactions. You will learn best practices for due diligence and current trends in indemnification. Lawrence will break down standard representations and warranties in physician practice transactions and how those representations tie to both due…
Medical Device Single Audit Program Preparation

Medical Device Single Audit Program Preparation

Location: , United States
Category: Health and Medicine
Start Date: 04-06-2018
Overview: The International Medical Device Regulators Forum (IMDRF) recognizes that a global approach to auditing and monitoring the manufacturing of medical devices could improve their safety and oversight on an international scale. Why should you Attend: Today with a single audit, it is possible for a medical device manufacturer to satisfy the quality management system requirements of Australia, Brazil, Canada, Japan and the USA! This is the benefit of the Medical Device Single Audit Program, or MDSAP. However, there are some vital considerations before embarking upon this approach to satisfying the regulators of five major markets. Areas Covered in the…
Compliance for Electronic Records and Signatures 2018

Compliance for Electronic Records and Signatures 2018

Location: , United States
Category: Health and Medicine
Start Date: 04-06-2018
Overview: This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to greatly increase productivity. Areas Covered in the Session: Which data and systems are subject to Part 11 What Part 11 means to you, not just what it says in the regulation Avoid 483 and Warning Letters Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation Ensure data integrity, security, and protect intellectual property Who Will Benefit: IT QA QC Laboratory Staff Managers GMP, GCP, GLP Professionals Speaker Profile: David Nettleton, is an FDA…

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