World Conference Calendar

32676 Conferences

Health and Medicinerss


Device Changes, FDA Changes, and the 510(k) - Webinar by GlobalCompliancePanel

Device Changes, FDA Changes, and the 510(k) - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 11-03-2010 Last Day: 11-03-2010
The majority of medical devices are cleared for marketing in the U.S. by the FDA under the 510(k) process. The FDA holds companies responsible for filing new 510(k)s when one change is major enough to impact safety / effectiveness, or when a series of lesser changes finally reach the "tipping point". This is a major headache. How can companies make that determination? How can they trigger such an analysis over the major change or the series of smaller changes. What approaches are required for product changes; for process changes. How is the process risk-based? How to maximize the process against…
Crisis Management and Risk Communication - Webinar by GlobalCompliancePanel

Crisis Management and Risk Communication - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 11-04-2010 Last Day: 11-04-2010
As your company's system continues to grow, the potential for "crisis issues" to occur grows proportionally. The concern for food safety to your customers and employees must be a constant area of focus for all operators in the system. Ultimately, how well your company manages the crisis situations it will make a significant difference in how your company brand is perceived in the public's eyes and how well it succeeds in today's highly competitive marketplace. Most important is that failure to ensure food safety can jeopardize the health of your customers and could be detrimental to your business and reputation.…
The 6th Annual World Healthcare Innovation and Technology Congress (WHIT v.6.0)

The 6th Annual World Healthcare Innovation and Technology Congress (WHIT v.6.0)

Location: , United States
Category: Health and Medicine
Start Date: 11-07-2010 Last Day: 11-10-2010
The 6th Annual World Healthcare Innovation and Technology Congress (WHIT v.6.0) is the leading event for senior executives tasked with making multi-million dollar strategic, organizational and IT decisions to position their organizations for success in the rapidly changing marketplace. WHIT v.6.0 brings together providers, payers, government officials and other key stakeholders to provide critical insight and leading-edge case studies on innovative technologies and strategies that will improve outcomes and minimize costs. ** Confirmed speakers include FIVE speakers whose organizations have reached Stage 6 or above on the HIMSS EMR Adoption Model(sm) and SIX speakers from H&HN's 2009 Health Care's 100…
Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process - Webinar By ComplianceOnline

Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process - Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 11-09-2010
This webinar will discuss the different aspects which auditors generally look in equipment calibration, maintenance and validation and highlight the best practices. Areas Covered in the Seminar: Equipment Validation: Installation Qualification, Operation Qualification, and Performance Qualification. Equipment Calibration Requirements. Equipment Preventive Maintenance Requirements. Calibration vs. Maintenance: When to use Which One? Remedial Action for Out-of-Calibration Equipment. Use of Calibration Standards to Save Cost. Equipment Calibration Requirements: Scheduling, Use of External Services, and Documentation. Equipment Preventive Maintenance Requirements. Use of Calibration Standards to Save Cost. Remedial Action for Out-of-Calibration Equipment. Calibration vs. Maintenance: Which One? Equipment Validation: Installation Qualification, Operation Qualification,…
Full Day Virtual Seminar - Designing and Implementing the Quality System for Combination Products - by GlobalCompliancePanel

Full Day Virtual Seminar - Designing and Implementing the Quality System for Combination Products - by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 11-10-2010 Last Day: 11-10-2010
The FDA generally defines combination products as a product composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device, and a biological product. Although there are differences between these quality systems, the quality principles embodied in the systems are the same. This course looks at these principles and the processes associated with each principal to design, implement, and maintain a combination system that surpasses compliance requirements. The seminar will focus primarily on the principles embodied in CFR Parts 210-211 and ICH Q7A for pharmaceuticals…
Good Documentation Practices in a Regulated Environment - Webinar By GlobalCompliancePanel

Good Documentation Practices in a Regulated Environment - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 11-16-2010 Last Day: 11-16-2010
Whether you work in production or in a laboratory or if you conduct investigations or finalize product release, sound data and information is essential to success and compliance. To ensure success, and avoid those frustrating, embarrassing discussions of missing or doubtful data, employees recognize and must follow Good Documentation Practices (GDP). These practices apply to all pharmaceutical and medical device manufacturing, and their support areas. GDP describes the required activities and steps to use when recording data and other handwritten entries. Personnel, who work with documentation must be informed of these requirements, recognize their significance to their job and be…
Intervention

Intervention

Location: , United States
Category: Health and Medicine
Start Date: 11-16-2010 Last Day: 11-16-2010
"Intervention" will be presented on Tuesday November 16, 2010, from 7:30 pm to 9:00 pm; by Jeff and Debra Jay; Intervention specialists, chemical dependency therapists and trainers, and best-selling authors of "Love First: A New Approach to Intervention for Alcoholism and Drug Addiction" and other books. This program will describe how the "Love First" process of Intervention can help chemically dependent people find recovery. Key elements of the "Love First" model for effective intervention with addicted individuals will be discussed. This program will bring PRACTICAL INFORMATION, HELP and HOPE to anyone who cares about a chemically dependent person, and to…
Are you a new Clinical Research Coordinator? Tips on how to get started, what to expect - Webinar By ComplianceOnline

Are you a new Clinical Research Coordinator? Tips on how to get started, what to expect - Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 11-17-2010
This clinical research webinar will discuss the role and responsibilities of an efficient well rounded Clinical Research coordinator and what to do pre and post trial period to comply with GCP and other regulations. Areas Covered in the Seminar: ICH guidelines and Good Clinical Practice (GCP). Types and Phases of Clinical Trials. Role and responsibilities of a Clinical Research coordinator. Key aspects of the role and key players involved in a trial. Role of the Principal Investigator. Education and Outlook. Activities that are common to most trials. Linking responsibility to these activities. Institutional Review Board/ Informed consent. Trial- from selection…
Process Verification and Validation - Webinar by GlobalCompliancePanel

Process Verification and Validation - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 11-17-2010 Last Day: 11-17-2010
This webinar will provide valuable guidance to regulated companies in development, implementation, or refinement of their manufacturing process verification and validation programs. It will evaluate validation practices that are more in agreement with ICH Q7 and Q8 than previously accepted validation methods, and will provide thought-provoking questions for FDA-regulated companies. Enhanced use of existing FDA tools by a company will be discussed. What are the expected industry trends for the future as indicated by recent FDA and other guidance documents, for which companies should now prepare? Why Should You Attend: The FDA expects companies to perform meaningful, results driven manufacturing…
Computer System Validation: Step-by-Step - Webinar by GlobalCompliancePanel

Computer System Validation: Step-by-Step - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 11-17-2010 Last Day: 11-17-2010
Learn computer system validation essentials and eight fundamental steps of implementation for cost saving. Get complementary SOPs and checklists for easy implementation. Understand the structure of validation plan, documentation of ongoing performance, structure of validation report. Why Should You Attend: The validation of computer system has been an FDA requirement since more than 20 years. Nevertheless companies have problems with implementation. This is proven through many FDA warning letters related to software and computer system validation, especially in the last three years. Validation professionals know the principles but have problems with implementation, especially with the development of protocols. This seminar…
The Drug Development Path - From R&D to Commercialization - Webinar by GlobalCompliancePanel

The Drug Development Path - From R&D to Commercialization - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 11-18-2010 Last Day: 11-18-2010
An overview of the drug development process, reviewing key deliverables for each stage of the development path with a special focus on managing the development process when using external resources such as Contract Manufactures, Contract Testing Labs and Contract Research Organizations. In today's fast-paced, highly regulated and risk-aversive environment, functional groups can no longer work in isolation, but must collaborate extensively to design, develop, manufacture, test, validate and commercialize new drugs. Successful commercialization depends on effective processes to bring both the drug supply manufacturing processes and controls as well as the associated data and knowledge to the levels required for…
Conducting Clinical Trials in Latin America: keys to successful study implementation - Webinar By ComplianceOnline

Conducting Clinical Trials in Latin America: keys to successful study implementation - Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 11-22-2010
This Clinical trial training will review the current status of Clinical Trials activities in Latin America, the factors that make this region such an attractive one and some best practices to ensure a successful implementation of clinical trials. Areas Covered in the Seminar: Overview of the Latin American region. Clinical Trials Activitiy in the Latin American countries. What explains the growth and success of the Region. Regulatory overview of the major contributing countries. Main Challenges in the conduct of Clinical Trials in Latin America. Keys to success in the conduct of Clinical Trials in Latin America. Who Will Benefit: This…
How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters - Webinar By ComplianceOnline

How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters - Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 11-23-2010
This GCP compliance in Clinical Trials training aims to provide an overview of the parameters critical in ensuring GCP compliance and in doing this, will translate GCP in a more practical, applied sense. Areas Covered in the Seminar: Importance of Good Clinical Practice. Key areas of deficiencies in Clinical trials. Common findings in audits and inspections. Definition of ranking of findings: minor-major-critical. Definition of Adverse and Serious adverse events. ICH guidelines on the Informed consent process. Management of investigational drug. Investigator site file and essential documents. Source data. Site and people management. Who Will Benefit: This webinar will provide valuable…
The Doctor's Opinion on Alcoholism

The Doctor's Opinion on Alcoholism

Location: , United States
Category: Health and Medicine
Start Date: 11-23-2010 Last Day: 11-23-2010
"The Doctor's Opinion on Alcoholism" will be presented on Tuesday November 23, 2010, from 7:30 pm to 9:00 pm; by Dr. Herbert Malinoff, MD; Addictionologist . This program will describe a physician's view of alcoholism, as presented in the literature of Alcoholics Anonymous and updated with the modern neurobiology of addictive illness. It will include a discussion of Dr. Silkworth's explanation of alcoholism as a twofold disease affecting mind and body, how Dr. Silkworth's opinion relates to the modern neurobiology of addictive illness, identification of therapy for alcoholism as promoted by Alcoholics Anonymous, and the relationship of this therapy to…
"Know Your Customer" - The DEA Due Diligence - Webinar By GlobalCompliancePanel

"Know Your Customer" - The DEA Due Diligence - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 11-30-2010 Last Day: 11-30-2010
Overview: This training will cover several recommendations to improve Due Diligence when distributing Schedules II through V controlled substances and regulated chemicals to your customers and what steps can be taken to prevent the illicit use or diversion of any product sold to a customer. As a firm handling these products, you will get a better understanding of what is required from a DEA registered Manufacturer or Distributor when a customerís order becomes an order of interest or identified as a suspicious order. Why should you attend: Understanding the DEA "Know Your Customer" Policy is important, and the steps suggested…
Suicide and Recovery from Addiction

Suicide and Recovery from Addiction

Location: , United States
Category: Health and Medicine
Start Date: 11-30-2010 Last Day: 11-30-2010
"Suicide and Recovery from Addiction" will be presented on Tuesday November 30, 2010; 7:30 pm to 9:00 pm; by Michelle Rose Armstrong , MA, LLP, and Michael B. Murphy, MA, LMSW (Members of Washtenaw Alive, a suicide prevention community collaboration.) This program will teach participants to be alert to the signs of suicidal thinking among individuals in recovery. It will help participants to recognize the signs of suicidal thinking, learn how to reach out and offer support, know how to reach out and ask for help when suicidal thoughts are present, and be aware of local and national suicide prevention…
Introduction to Operational Risk - Webinar By GlobalCompliancePanel

Introduction to Operational Risk - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 12-01-2010 Last Day: 12-01-2010
This three hour overview of financial risk management will provide the fundamentals to risk management that all managers need to comprehend. Regardless of job titles, risk management is a shared responsibility by all managers. Compared to accounting, risk is an immature discipline with a variety of risk frameworks competing to dominate. Based on the new Wiley and Sons book, Essentials of Risk Management, due for publication at the end of 2010, this webinar is designed to provide a non-math introduction to an area and discipline that is changing rapidly, especially in the light of the risk management failures that have…
Recalls of Medical Devices in the US - Medical Device Webinar By ComplianceOnline

Recalls of Medical Devices in the US - Medical Device Webinar By ComplianceOnline

Location: , United States
Category: Health and Medicine
Start Date: 12-02-2010 Last Day: 12-02-2010
In this Medical device recall training learn how to interface with FDA in regards to anticipated recalls, the communication, the response, how to prepare the public information. Areas Covered in the Seminar: - Recent product recall failures. - Analyzing product risks. - CAPA prioritization. - Communicating with FDA. - Deciding on the response. - Preparing the public information. - Notifying the customers. Who Will Benefit: - Medical Device managers - CAPA Managers - Quality Managers - Regulatory Compliance Managers - Product Management - Public Relations personnel - Marketing Management
Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel

Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 12-02-2010 Last Day: 12-02-2010
Overview: This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the global regulatory landscape. It is assumed that participants and customers have a prior CE Mark and Medical Device Directive background. The Technical File is a comprehensive collection of information and documents that details everything about your medical device. Understanding how to assemble this information and present the information properly is essential. If you manufacture a Class I device, a less complex CE Marking Technical File may be required. In the case of Class IIa, IIb…
The World Health Care Congress Middle East

The World Health Care Congress Middle East

Location: , United Arab Emirates
Category: Health and Medicine
Start Date: 12-05-2010 Last Day: 12-07-2010
The World Health Care Congress Middle East, co-sponsored by the Health Authority and the Tourism Authority of Abu Dhabi, is the most prestigious health care, convening more than 500 global thought leaders and key decision-makers from all sectors of health care to share global best practices. The 2010 Congress will take place 5-7, December 2010, Abu Dhabi, UAE. The Congress will feature the top industry influencers, including health ministers, leading government officials, hospital directors, IT innovations, pharmaceutical and medical device companies and health care industry suppliers. Register by December 5 and save $200 when you call World Congress at 800-767-9499…

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