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Software Verification and Validation Planning

Software Verification and Validation Planning

Location: , United States
Category: Health and Medicine
Start Date: 08-24-2010 Last Day: 08-24-2010
In this Software Verification and Validation training Understand and recognize the most common software V&V failings and their fixes. Learn how to develop and use a repeatable software V&V template for all software validation projects. Areas Covered in the Seminar: - Tougher FDA Expectations / Requirements. - Roles of Verification and Validation. - An FDA "Model". - A Typical Software V&V Protocol / Test Report. - A Brief Overview of 21 CFR Part 11. - Legacy, Hybrid, New and ER / ES Systems. - Expected Regulatory Deliverables. - Complementary Guidelines, e.g., GAMP. For More Details: http://bit.ly/ardQsg
35th International Symposium on Mathematical Foundations of Computer Science

35th International Symposium on Mathematical Foundations of Computer Science

Location: , Czech Republic
Category: Mathematics and Statistics
Start Date: 08-23-2010 Last Day: 08-27-2010 Deadline for abstracts: 04-10-2010
MFCS Symposia The series of MFCS symposia, organized in rotation by Poland, Slovakia, and the Czech Republic since 1972, has a long and well-established tradition. The symposia encourage high-quality research in all branches of theoretical computer science. Their broad scope provides an opportunity to bring together researchers who do not usually meet at specialized conferences. Quality papers presenting original research on theoretical aspects of computer science are solicited. The 35th International Symposiums on Mathematical Foundations of Computer Science (MFCS 2010) is organized in parallel with the 19th EACSL Annual Conferences on Computer Science Logic (CSL 2010) at the same place.…
The 8th International Conference on Recirculating Aquaculture

The 8th International Conference on Recirculating Aquaculture

Location: , United States
Category: Physical and Life Sciences
Start Date: 08-20-2010 Last Day: 08-22-2010
ICRA topics are still developing. We encourage those who may be interested in the ICRA to save the date. Those who wish to submit potential ICRA topics should email Terry Rakestraw at aqua@vt.edu
On Morals, Markets and Money – Economic and Business Ethics Revisited

On Morals, Markets and Money – Economic and Business Ethics Revisited

Location: , Germany
Category: Business and Economics
Start Date: 08-19-2010 Last Day: 08-22-2010 Deadline for abstracts: 03-01-2010
The crisis of the financial markets has led to a crisis in the economic systems internationally. The concepts of more market liberalization and markets as places of self-organization have gone into turmoil. There are different levels at which the economic developments can be discussed ethically On the political level both greater transparency and more regulation in the economic sphere are discussed in relation to different economic policies. Where is globalization heading, and what about aspects of justice concerning North-South relations globally as well as gender issues? Is there a global need for a European-inspired “Social Market Economy”? What are the…
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…
4th IEEE International Workshop on e-Activity (IEEE-IWEA2010)

4th IEEE International Workshop on e-Activity (IEEE-IWEA2010)

Location: , Japan
Category: Computer Science and Internet
Start Date: 08-18-2010 Last Day: 08-20-2010 Deadline for abstracts: 03-20-2010
IEEE-IWEA2010 is The 4th International Workshop on advances in theory, systems, and applications for all electronic activities, which include e-learning, e-commerce, and several other activities. The aim of this workshop is to encourage activities in this field, and to bring together WWW researchers with e-activities. Unlike conventional conferences, this workshop will mainly discuss and explore scientific and practical problems as raised by the participants. The focus of the workshop will be on computer science, cognitive science, web technology, artificial intelligence, multi-agent systems on the web, WWW, semantic web, etc. In particular, the workshop will bring together researchers from Computer technology…
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…
AMO Annual Conference 2010

AMO Annual Conference 2010

Location: , Canada
Category: Interdisciplinary
Start Date: 08-15-2010 Last Day: 08-18-2010
2010 AMO Annual Conference August 15 - 18, 2010 at the Caesars Windsor Hosted by The City of Windsor and the County of Essex The AMO Annual Conference is a gathering of municipal government officials and each year offers a program theme related to current and emerging issues. A wide range of sessions provide delegates with the opportunity to learn and network to then take back to their respective communities new ideas and solutions. The exhibitor hall, always a sold-out event, is another means of networking with the exhibitors and other delegates. For information on exhibiting, sponsoring or attending the…
The 5th IUPAC International Symposium on Macro- and Supramolecular Architectures and Materials (MAM-10): New Science and Technologies for the Improvement of Human Living Standards

The 5th IUPAC International Symposium on Macro- and Supramolecular Architectures and Materials (MAM-10): New Science and Technologies for the Improvement of Human Living Standards

Location: , Jamaica
Category: Interdisciplinary
Start Date: 08-15-2010 Last Day: 08-20-2010 Deadline for abstracts: 05-30-2010
As novel materials will play a key role in science and technology in the 21st century, the objectives of this symposium series are in providing an interdisciplinary forum for scientists engaged in the full spectrum of research, development, application, and to discuss the current status and recent developments of these materials with a focus on the new science and technologies for the improvement of human living standards. In addition, the meeting will provide an opportunity to overview the field by covering a wide range of topics. Themes have selected to accommodate a wide range of interests to facilitate interdisciplinary interactions…
Mission Possible: Taking Control of the Metabolic Syndrome

Mission Possible: Taking Control of the Metabolic Syndrome

Location: , United States
Category: Education
Start Date: 08-12-2010 Last Day: 08-22-2010
This program is designed for primary care nurses, nurse practitioners, and learners will gain an understanding of the metabolic syndrome, the complications associated with this, and assist their patient’s in their ability to manage their chronic disease. This is a land study Tour of Italy, and our conference sessions will be held in Rome and Bologna.
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…

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