World Conference Calendar

31707 Conferences

Health and Medicinerss


Corporate Governance & Compensation in Risk Management - Webinar by GlobalCompliancePanel

Corporate Governance & Compensation in Risk Management - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-07-2010 Last Day: 09-07-2010
This session will provide an overview of the major tenants of corporate board governance, structure, organization, and composition and how each of these relates to an enterprise's ability to balance risk and opportunities while acting in an ethical and prudential manner which addresses all its stakeholders - investors, employees, customers, suppliers, creditors, regulators, and taxpayers. Areas covered include: * How corporate boards failed investors in the global financial crisis * The need for executive level compensation reform * The proven benefits in increased corporate board diversity * The benefits of a board-level risk committee Why Should You Attend: The popular…
Post-Design Medical Device Risk Management - Webinar by GlobalCompliancePanel

Post-Design Medical Device Risk Management - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-07-2010 Last Day: 09-07-2010
In this presentation we will explore the requirements for post-design risk management and determine how to apply the requirements. The presentation is conceived as a practical demonstration of how to meet post-design requirements of ISO 14971. We will review the production and post-production requirements of ISO 14971 as stated in Clause 9 and interpret their meaning for the medical device industry. The presentation will use practical examples of the application and use of risk management information as well as determine when risk management files need to be updated. We will also review the requirements for Management Review of risk management…
Improving Sanitation Standard Operating Procedures in the Food Industry  - Webinar by GlobalCompliancePanel

Improving Sanitation Standard Operating Procedures in the Food Industry - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-07-2010 Last Day: 09-07-2010
Foodborne illness is often traced to improper cleaning and sanitizing of food equipment and the environment. Operators of food facilities develop and implement Sanitation Standard Operating Systems to protect food from contamination. Specifics about the people, equipment, facility, cleaning and sanitizing methods and procedures must be carefully documented. Foodborne illness is often traced to improper cleaning and sanitizing of food equipment and the environment. Investigators point to failures of basic sanitation in recent nationwide outbreaks involving peanut butter, potpies and, spinach. Scientific systems such as Hazard Analysis Critical Control Point (HACCP) require the operator to control the potential for environmental…
Engineering and Laboratory Mythology with Water System

Engineering and Laboratory Mythology with Water System

Location: , United States
Category: Health and Medicine
Start Date: 09-08-2010 Last Day: 09-08-2010
This water systems webinar training will discuss the myths surrounding microbial monitoring and control approaches and alert you to the pitfalls of believing these myths which could cause over-confidence in a systemís design for microbial control or the suitability of your microbial test methods. Areas Covered in the Seminar: - Why water myths develop. Impact of c-GMPs Well-meaning but misguided precedents Scientifically unchallenged traditions and benchmarking Rule-hungry culture - Water System Microbial Control Myths. WFI from RO Turbulent Flow and Flow Rate Dead Leg Rules Smooth Surfaces In-Line Sterilizing Filters Ozone - Microbial Enumeration Myths. Referee Methods Thermopiles in Hot…
Key Modules of an Effective CAPA SOP - Webinar by GlobalCompliancePanel

Key Modules of an Effective CAPA SOP - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-08-2010 Last Day: 09-08-2010
This webinar will examine the stated intent of the Agency to get tougher across the board in its expectations for the medical industry and its compliance to the cGMPs, especially CAPA. It will examine how these goals of the Agency have translated into action in the past half year, with trends evident in 483 observations and Warning Letters. A key to effective relations with the FDA is the emphasis on proving a company is "in control" to an investigator's satisfaction, which has to center on CAPA. So the webinar will address the development of a new, or revision of an…
Effective & Essential CAPA process to avoid FDA 483 - Webinar by GlobalCompliancePanel

Effective & Essential CAPA process to avoid FDA 483 - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-08-2010 Last Day: 09-08-2010
How do you prevent becoming another FDA statistic? Poor corrective and preventive action (CA/PA) and investigations continue to be among top FDA Form 483 deficiencies issued to drug, biologic, and medical device manufacturers. It's in everyone's self interest to improve the quality of investigations and CA/PA. This webinar will provide regulated companies the core principles and practices needed to implement an effective and efficient CA/PA process. This presentation will begin by defining risk in compliance and the methods, which can be used to mitigate risk. One of the methods defined by the regulators and the industry is "Corrective Action /…
Key Factors to Write an Effective Standard Operating Procedure (SOP)

Key Factors to Write an Effective Standard Operating Procedure (SOP)

Location: , United States
Category: Health and Medicine
Start Date: 09-09-2010 Last Day: 07-09-2010
In this Effective Standard Operating Procedure (SOP) training learn how to develop a comprehensive, consistent SOP. The critical elements of a SOP which is easier to understand follow and review by operating personnel. Areas Covered in the Seminar: - Define elements of an SOP. - Establish SOP change control system. - Ensure that the instructions and details in the SOPs are sufficient and consistent. - Train personnel on reviewing and understanding the SOPs. - Develop an effective and comprehensive training program For More Details: http://bit.ly/9MENNo
Verification of Pharmacopeia Methods  - Webinar by GlobalCompliancePanel

Verification of Pharmacopeia Methods - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-09-2010 Last Day: 09-09-2010
Laboratories that work in a GMP environment are required to have documentation to show they are qualified to run specific, consistent and reliable analytical test methods. Method qualification of a method can be achieved in three ways: Validation, Verification (Compendial Methods) and Method Transfer (company methods). Lack of such documentation can result in warning letters from both the FDA and Health Canada. This webinar explains the reason and purpose of USP chapter and helps you to interpret what is required for verification of pharmacopeia methods to satisfy regulatory requirements. It discusses how to select appropriate analytical performance characteristics and acceptance…
Signal Detection and Data Mining  - Webinar by GlobalCompliancePanel

Signal Detection and Data Mining - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-09-2010 Last Day: 09-09-2010
This webinar will cover the fundamentals of signal detection, and how these can be augmented by the use of data mining techniques. In March 2005, the FDA published final guidance on "Good Pharmacovigilance Practices and Pharmacoepidemiologic Assessment." This guidance defines the FDA's views on pharmacovigilance concepts, safety signal identification, pharmacoepidemiologic assessment and interpretation of safety signals. This webinar will demonstrate how to meet FDA's requirements for detection of potential signals or trends. Why should you attend: The requirement for companies to perform signal detection is now mandatory in Europe and highly recommended in the US. The FDA Amendment Act mandates…
Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11 - Prepare Yourself for the upcoming FDA Part 11 Inspections - Webinar by GlobalCompliancePanel

Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11 - Prepare Yourself for the upcoming FDA Part 11 Inspections - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-09-2010 Last Day: 09-09-2010
On July 8, 2010, the FDA announced to soon conduct a series of inspections related to 21 CFR Part 11. FDA made it very clear that the focus of the inspections will on most critical issues the industry had with Part 11 in the past. The best way to find out what the issues are is to look at recent FDA 483 form inspectional observations and warning letters related to computer system validation and Part 11 compliance. Just from 2007-2010, there have already been more than 30 such warning letters, some with disastrous consequences for inspected companies. This seminar will…
2nd Successful eCTD Lifecycle Management

2nd Successful eCTD Lifecycle Management

Location: , Czech Republic
Category: Health and Medicine
Start Date: 09-14-2010 Last Day: 09-15-2010
Pharma IQ is delighted to announce the 2nd Successful eCTD Lifecycle Management conference, being held in Prague on the 14th and 15th of September 2010. With eCTD submissions taken a firm hold in the US and Japan, they are now making their mark in Europe. Now eCTD submissions are becoming the preferred format for regulatory submissions in Europe so it is essential that you are equipped with in-house expertise and external solutions to ensure first time compliance and submission success! This is a challenging area for all and is not something that can be easily avoided. This is your chance…
Developing an ethylene oxide (EO) sterilization process for a product with limitations

Developing an ethylene oxide (EO) sterilization process for a product with limitations

Location: , United States
Category: Health and Medicine
Start Date: 09-14-2010 Last Day: 09-14-2010
This EO sterilization training Webinar will discuss how to modify EO sterilization process for complicated medical products which are sensitive to moisture, temperature, vacuum changes. Areas Covered in the Seminar: - How to limit moisture exposure. - Running a low temperature process. - How to address vacuum sensitivity. - Parameter inter-relationships. - How to reduce EO residuals. - Testing outside of the sterilization facility. - Considerations for validation and routine processing. For More Details: http://bit.ly/cVoiXs
Understanding Acceptance Activities for Medical Devices - Webinar by GlobalCompliancePanel

Understanding Acceptance Activities for Medical Devices - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-14-2010 Last Day: 09-14-2010
Acceptance activities are common in device manufacturing, but seem to cause problems for some manufacturers. These problems range from simple instances of lack of procedures or acceptance criteria to misapplication of statistical methods. This webinar will clear up the regulatory requirements, and help you plan effective and compliant acceptance activities. We look at the regulations and explain what they mean. In addition, we look at the QSR preamble to help clarify the intent and expectations. FDA published the QSR manual to help manufacturers implement the regulations. The FDA's Quality system Regulation (QSR) sets requirements for acceptance activities related to medical…
Physical Properties Analytical and Screening Techniques - Webinar by GlobalCompliancePanel

Physical Properties Analytical and Screening Techniques - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-14-2010 Last Day: 09-14-2010
The chemical composition of the active ingredient of a pharmaceutical dosage form determines the efficacy and stability of the formulation however during manufacturing it is the physical properties of the formulation components that are critical in the unit operations. In order to evaluate the physical properties of a solid it is important to have reliable and reproducible analytical techniques. However the techniques available are not as direct and unambiguous as the chemical techniques available for purity, impurities etc. This seminar will provide an introduction to these physical analytical and screening techniques, the desired ranges and suggestions concerning their application. Why…
Auditing API Manufacturers and Suppliers - Webinar by GlobalCompliancePanel

Auditing API Manufacturers and Suppliers - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-14-2010 Last Day: 09-14-2010
This program will focus on the basics needed to perform an API audit. Performing an audit is not simply an act of visiting a firm and checking off a list of questions. Auditing API producers and suppliers is an important part of GMP compliance programs. Identifying what approach or process to use is examined and the tools to utilize during an audit is also discussed. Audits at best are snapshots of what exists at the moment of the audit; however, a good audit or auditor will be able to uncover the less obvious signals and signs of concern. Learn what…
Troubleshooting ethylene oxide (EO) processes - Webinar by GlobalCompliancePanel

Troubleshooting ethylene oxide (EO) processes - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-15-2010 Last Day: 09-15-2010
Not every parameter in the EO sterilization process in critical for the determination of the SAL. This presentation will outline the various parameters and what actions should be taken when they are not compliant to the process specification. These actions may be as simple as a rationale for release to as complicated as the need for the qualification of a new sterilization process. How to decide the course to take will be addressed along with the reasons behind the decisions so that an accurate and complete justification of your decision can be made for both management and regulatory agencies. The…
Medical Devices in the EU: CE Mark and 93/42/EEC Directive

Medical Devices in the EU: CE Mark and 93/42/EEC Directive

Location: , United States
Category: Health and Medicine
Start Date: 09-16-2010 Last Day: 09-16-2010
This webinar will provide valuable assistance and guidance to all regulated companies that are preparing for CE Mark and ensuring compliance to MDD 93/42/EEC. Areas Covered in the seminar: . Identify the steps required to obtain CE MarkÖand meeting compliance expectations. . Understand how to apply and use the Conformity Assessment Procedure. . How to classify your medical device correctly? . Learn how to use the Technical File correctly. . How to apply the Declaration of Conformity and why this is critical for success? . How ISO 13485 fits in with this process as a device company? . Learn and…
Law Enforcement and Pain Management - Webinar by GlobalCompliancePanel

Law Enforcement and Pain Management - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-16-2010 Last Day: 09-16-2010
Class participants will familiarize themselves with the federal laws and regulations enforced by DEA pertaining to Schedules II though V controlled substances that are dispensed, or prescribed by a physician as part of a pain treatment plan. Also they will be familiarized with the necessary documentation that should be noted in the patient chart and step to prevent diversion of the dispensed or prescribed drugs. Why should you attend: As a pain management clinic or physician treating pain, you are required by federal and state laws and regulations to take many steps in order to be assured that the controlled…
FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes - Webinar by GlobalCompliancePanel

FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 09-16-2010 Last Day: 09-16-2010
Marketing wants to entice customers to buy your product instead of your competitor's! A common method is to make the labeling as eye-catching as possible. Be careful! You need to know what information can (and more importantly) CANNOT be present on the labeling. This presentation provides comprehensive knowledge of labeling development and subsequent control. FDA requirements and expectations regarding labeling contents will be covered, as will recommended practices to assure substantial compliance. Areas Covered in the Session: * Prescription Device Labeling * Misbranding, False Or Misleading Labeling * Approval * Issuance * Label Integrity * Label Inspection * Contractor-Produced Labels…
End of Life Issues: Ethical and Religious Perspectives

End of Life Issues: Ethical and Religious Perspectives

Location: , United States
Category: Health and Medicine
Start Date: 09-17-2010 Last Day: 09-18-2010
IMANA-Hofstra Ethics Symposium The Islamic Medical Association of North America (IMANA) and the Muslim Chaplainís Office of Hofstra University invite you to attend the 2010 IMANA-Hofstra Ethics Symposium, September 17-18, 2010. The symposiumís theme is End of Life Issues: Ethical and Religious Perspectives. Intended audience are physicians, especially those in critical care medicine, emergency medicine, maternal fetal medicine and neonatology, medical bioethicists, chaplains, students in these fields and interested individuals.

<< Start < Prev 1 2 3 4 5 6 7 8 9 10 Next > End >>

© 2017 World Conference Calendar. All rights reserved.
About WCC | News | FAQs | Links | Terms and Conditions | Privacy | Contact Us