World Conference Calendar

32676 Conferences

Health and Medicinerss


Defining, Architecting and Managing Risk Assessments - Webinar by GlobalCompliancePanel

Defining, Architecting and Managing Risk Assessments - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-19-2010 Last Day: 08-19-2010 Deadline for abstracts: 08-18-2010
Risk Assessments are a vital tool in the Risk and Compliance management arsenal. Unless a business knows at any given time what its exposures are, and how they are evolving, the mitigation steps to manage its risks can never be in lockstep with prevailing circumstances or conditions. Concise Risk Assessments are a vital component of any successful Risk based initiative. Intelligent enquiry is an art that is often little understood. How Risk Assessments are created, distributed, collated and analyzed can be the difference between risks detected and managed, and the unwelcomed and often catastrophic risk event. Why should you attend:…
Best Practices in Complaint Management - Webinar by GlobalCompliancePanel

Best Practices in Complaint Management - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-19-2010 Last Day: 08-19-2010 Deadline for abstracts: 08-18-2010
Negative customer feedback about a medical device's performance or safety is a strong indicator of whether a firm's manufacturing process is in control. This feedback is therefore subject to many requirements in both the QSR and ISO 13485. Failure to follow up on complaints about medical devices is among the most frequently cited observations on FDA-483s. This session will include the requirements for defining, documenting, and implementing a complaint-handling system, including the requirements for complaint review, investigation, and corrective action, as well as the ISO-specific implications. This session will discuss the best way to document customer feedback, what constitutes a…
Important Sterilization Information for Product Developers - Webinar by GlobalCompliancePanel

Important Sterilization Information for Product Developers - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-19-2010 Last Day: 08-19-2010 Deadline for abstracts: 08-18-2010
Product developers have the responsibility of the development of medical devices or healthcare products that will be sterilized; however they may not have an adequate understanding of the sterilization processes and its impact to the functionality of the product and its package. This presentation will provide information that can be used by R&D Engineers and Product Developers to aid them in the selection of materials, design characteristics and appropriate packaging by providing them with a basic knowledge of what is involved in the process of sterilization. It will also provide guidance on how the sterilization process can be changed to…
Change Control and Logging in the PCI environment - Webinar by GlobalCompliancePanel

Change Control and Logging in the PCI environment - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-19-2010 Last Day: 08-19-2010 Deadline for abstracts: 08-19-2010
Change control in IT environments has been a focus for a decade or so, especially for application changes. In this webinar you will learn: The components of a strong change management program, including specifics on configuration management, system hardening, and compliance review. In addition, the types of logging and monitoring required by the PCI DSS will be discussed which will enable confidence in approaches and tools that will meet the intent of the requirement and establish security. Why Should You Attend:Configuration changes are also important to document and test and standards like the PCI DSS have brought this topic to…
Construct and Manage the Technical File and Design Dossier

Construct and Manage the Technical File and Design Dossier

Location: , United States
Category: Health and Medicine
Start Date: 08-19-2010 Last Day: 08-19-2010
This CE technical files based training Webinar will discuss the difference between Technical File and Design Dossier and explain how to create them and the best practices. Areas Covered in the Seminar: - Learn the differences between the Tech File and Dossier and why the construction phase is so important. - Compile the EU Technical File or Design Dossier and ensure - Format and Content expectations are addressed appropriately. - Understand why Design Dossier is viewed as a subset of the Tech Documentation with emphasis on “design”. - Determine exactly which materials need to be assembled. - NB must examine…
Failure Modes and Effects Analysis (FMEA) - An Effective Tool for Medical Device Risk Management - Webinar by GlobalCompliancePanel

Failure Modes and Effects Analysis (FMEA) - An Effective Tool for Medical Device Risk Management - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-18-2010 Last Day: 08-18-2010 Deadline for abstracts: 08-17-2010
Most medical device manufacturers use FMEA as a part of their risk management system. Risk Management is required by ISO 13485 and risk analysis by the FDA's Quality System Regulations (QSR) and by of the EU medical device regulations. Using practical examples, this course look at the regulatory and reporting requirements of EN ISO 14971, "Medical devices - application of risk management to medical devices". The FMEA tool is used to provide an understanding of risk management and risk analysis techniques and methodologies, and to develop the skills required to apply these methodologies appropriate to a particular product. Risk management…
Auditing a Process-based System - Webinar by GlobalCompliancePanel

Auditing a Process-based System - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-18-2010 Last Day: 08-18-2010 Deadline for abstracts: 08-17-2010
The structure of ISO 9001:2000 provides a focus on the processes that comprise the quality management system (QMS). Also, the general requirements in Clause 4.1 state that the organization must identify all processes of the QMS, their sequence and interaction, and must ensure their effectiveness and the availability of needed resources, and monitor, measure, analyze and improve them. The characteristics defined in Clause 4.1 are a foundation for auditing a process-based system. Additional information used by auditor includes identifying the process owners, inputs and outputs, suppliers and customers, controls and resources of each process. Using this information, the audit team…
Pharmaceutical Manufacturing Batch Record Review - Webinar by GlobalCompliancePanel

Pharmaceutical Manufacturing Batch Record Review - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-18-2010 Last Day: 08-18-2010 Deadline for abstracts: 08-17-2010
The FDA and its European counterpart, EMA, require drug manufacturers to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate compliance. An efficient and effective batch record review process provides pharmaceutical companies with two strategies. First, this effort is key to maintaining control of your firm's manufacturing operations, eliminating any guesswork and aiding in the resolution of atypical occurrences. And, it enables a company’s to maintain and demonstrate a compliant posture, a sure way to avoid any quandary with…
Troubleshooting ethylene oxide (EO) processes

Troubleshooting ethylene oxide (EO) processes

Location: , United States
Category: Health and Medicine
Start Date: 08-17-2010 Last Day: 08-17-2010
This EO sterilization training Webinar will discuss the important parameters to measure for the sterility assurance level and actions to take if they are not compliant to the process specification. Areas Covered in the Seminar: - What is a cycle anomaly. - What cycle specifications are critical for sterilization. - What cycle specifications are critical for product residuals. - Actions to be taken for critical deviations/anomalies. - Actions to be taken for non-critical deviations/anomalies. - What testing can be performed to justify product release. - Developing a specification to address actions. - How to document your rationale. For More Details:…
Conduct Your Own Risk Assessments Following ISO Standard 31000/31010 - Webinar by GlobalCompliancePanel

Conduct Your Own Risk Assessments Following ISO Standard 31000/31010 - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-17-2010 Last Day: 08-17-2010 Deadline for abstracts: 08-16-2010
For the last decade, there has been an extensive and organized effort by organizations to assess their risks, especially in financial services. The new ISO 31000 and ISO 31010 frameworks provide guidelines in this process that make good sense and build on decades of work by risk professionals Why you should attend: It is essential for any organization to first determine its risk appetite and then to conduct its own self assessment as to its actual risk exposure. The new ISO risk standards provide a straight forward method that is suitable for larger and smaller organizations alike. Aligning your risk…
How to Survive a DEA Audit - Webinar by GlobalCompliancePanel

How to Survive a DEA Audit - Webinar by GlobalCompliancePanel

Location: , United States
Category: Health and Medicine
Start Date: 08-17-2010 Last Day: 08-17-2010 Deadline for abstracts: 08-16-2010
This training entitled "How to Survive a DEA Audit" will cover all the record-keeping and security requirements that a DEA registrant must comply with when handling controlled substances and regulated chemicals. It covers all elements of what occurs during an unannounced DEA Diversion inspection and the auditing of all controlled substances and regulated chemicals. As a firm handling these products, you will get a better understanding of what is required from a DEA registered manufacturer or distributor. Why Should You Attend: When DEA Diversion personnel conducts an unannounced inspection to perform an audit on a premise that is registered as…
Outsourcing Clinical Trials in Latin America

Outsourcing Clinical Trials in Latin America

Location: , United States
Category: Health and Medicine
Start Date: 08-12-2010 Last Day: 08-12-2010
This clinical trial training will review some Outsourcing Models that have been used successfully in the Latin American countries where Clinical Research is developed, identifying best practices and opportunities that speed protocol approval in these countries. Areas Covered in the Seminar: - Overview of the Latin American region. - Clinical Trials Activitiy in the Latin American countries. - Outsourcing Capabilities for Clinical Research In Latin America. - Review of available outsourcing providers and their service options. - Opportunitites for Increased efficiency. - Succesful outsourcing models Note: Use this Promo Code(100120) to avail Discount of 10% on LIVE Purchase. For More…
Principles and Practices of Traceability and Calibration

Principles and Practices of Traceability and Calibration

Location: , United States
Category: Health and Medicine
Start Date: 08-12-2010 Last Day: 08-12-2010
In this Calibration training learn and understand different types of measurements units, measurement constants, calibration and measurement standards as well as principles and practices of traceability. Areas Covered in the Seminar: - Base SI Units. - Derived SI Units. - SI Multipliers and Conversions. - Fundamental Constants. - Common Measurements. - Principles and Practices of Traceability. - Types of Measurement Standards. - Substitution of Calibration Standards. For More Details: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701644?channel=worldconf
Defining and Managing Protocol Deviation/Violation/Exception

Defining and Managing Protocol Deviation/Violation/Exception

Location: , United States
Category: Health and Medicine
Start Date: 08-10-2010 Last Day: 08-10-2010
In this GCP Webinar training, learn how to proactively predict and manage Protocol Deviation/Violation/Exception. Understand the guidance for implementation of “Protocol Not Followed” (PNF). Areas Covered in the Seminar: - How to define and manage Protocol Deviation/Violation/Exception. - Proactive approaches to predict and prevent clinical trial protocol violations. - Industry and FDA perspectives on Protocol Deviation/Violation/Exception. - Discuss the current lack of unified definition for protocol deviation/violation/ exception. - Define the term “Protocol Not Followed” (PNF). - Explain the guidelines for the implementation of PNF to include capturing, reporting, and documentation. - Review recent noncompliance trends and regulatory focus for…
How Accurate Adverse Event Reporting is the Key to Subject Safety of approved drugs

How Accurate Adverse Event Reporting is the Key to Subject Safety of approved drugs

Location: , United States
Category: Health and Medicine
Start Date: 08-04-2010 Last Day: 08-04-2010
In this Clinical compliance training learn how to assess record and manage the adverse events occurring during conduct of clinical research utilizing human subjects and how to avoid the common mistakes. Areas Covered in the Seminar : The CFR definitions of Adverse Events, Serious Adverse Events, Unanticipated Adverse Device Effects and many more. How to know what an Adverse Event is and when to report it or them. Understanding laboratory AEs and the "Reference Range" concept. Common Mistakes in AE / SAE Reporting. Reporting of Adverse Events - when and to whom and the use of AE Terminology systems The…
Reducing Ethylene Oxide (EO) Sterilization costs while maintaining regulatory compliance

Reducing Ethylene Oxide (EO) Sterilization costs while maintaining regulatory compliance

Location: , United States
Category: Health and Medicine
Start Date: 07-06-2010 Last Day: 07-06-2010
In this Ethylene Oxide (EO) Sterilization training learn how to evaluate your sterilization process for cost reduction, and will learn how to implement such changes without jeopardizing product safety and regulatory compliance. Areas Covered in the Seminar: -Introduction. -Factors Influencing Lethality and Aeration. -Finding Opportunities for Cycle Optimization. .Negotiate cost reduction .Initial Validation Evaluation Microbiological Method Cycle Parameters Evaluation EO residues dissipation curves Product Evaluation - Cycle/Process Re-engineering .BI Incubation reduction .Parametric Release .PCD/Packaging/Pallet modification .Lethality curve development .Aeration modification - References. Note: Use this Promo Code(101902) to avail Discount of 10% on LIVE Purchase. For More Details: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701616?channel=worldconf
Critical Appraisal - Read Clinical Papers With Confidence

Critical Appraisal - Read Clinical Papers With Confidence

Location: , United Kingdom
Category: Health and Medicine
Start Date: 05-14-2010 Last Day: 05-14-2010
The critical appraisal classroom course by Superego Cafe has rapidly established itself as a leading course on the practice of evidence-based medicine. Our unique back-to-basics approach has enabled us to teach this subject effectively to a wide range of healthcare professionals. Most of our delegates are doctors but past delegates have also included dentists, pharmacists, nurses, researchers, medical librarians, managers and members of the pharmaceutical industry. Learning objectives: * Define ‘evidence-based medicine’ and discuss the importance of critical appraisal skills * Identify different study designs and demonstrate an awareness of the hierarchy of research evidence * Evaluate the methodology of…
Pre-Filled Syringes Americas

Pre-Filled Syringes Americas

Location: , United States
Category: Health and Medicine
Start Date: 04-12-2010 Last Day: 04-14-2010
Pre-filled syringes and injection devices are now regarded as the delivery method of choice for a wide range of parental products. According to industry research, the current market for pre-filled syringes is expected to reach 2.5 billion units by 2010. The growth rate is to be expected to remain at a high level of more than 10% annually due to a number of factors such as greater medication safety and increased convenience from using a pre-fillable device. However, there are some challenges and potential threats to syringe and needle supply manufacturers. Visiongain is proud to present Pre-filled Syringes Americas, which…
Battlefield Healthcare 2010

Battlefield Healthcare 2010

Location: , Germany
Category: Health and Medicine
Start Date: 03-23-2010 Last Day: 03-25-2010
The Battlefield Healthcare conference has been held annually in Europe since 2007 and with delegates from 16 countries attending the last meeting in March 2009, it is widely considered to be the most influential and important combat casualty care conference in Europe. Defence IQ’s Battlefield Healthcare 2010 will provide an opportunity for key figures in the military medical community to share operational updates, future requirements, and new medical techniques in pre operative care, surgery and rehabilitation. Key discussions will focus on: • Feedback from front line casualty care in Afghanistan including, tactical medicine, lessons from the RAF MERT, Role One…
2010 International Conference on Biotechnology and Food Science (ICBFS 2010)

2010 International Conference on Biotechnology and Food Science (ICBFS 2010)

Location: , India
Category: Health and Medicine
Start Date: 02-12-2010 Last Day: 02-13-2010 Deadline for abstracts: 10-15-2009
The 2010 International Conference on Biotechnology and Food Science (ICBFS 2010) will be held in Bangalore, India during February 9-11, 2010. The aim objective of ICBFS 2010 is to provide a platform for researchers, engineers, academicians as well as industrial professionals from all over the world to present their research results and development activities in Biotechnology and Food Science. This conference provides opportunities for the delegates to exchange new ideas and application experiences face to face, to establish business or research relations and to find global partners for future collaboration. Submitted conference papers will be reviewed by technical committees of…

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