Online Event
Why Should You Attend:
Although the term, Quality Manual, is mentioned quite frequently in the pharmaceutical and medical device industries, are you aware that the quality manual has not always been included as a requirement in these regulations? Only in recent years has its valuable role been recognized as a tool that holds the quality system together. Read more »
Online Event
Why Should You Attend:
In order for a medical device company to meet the requirements for a CE mark, the software must be developed in a manner that meets the requirements of IEC 62304, “Medical device software-Software life cycle processes.” Read more »
Online Event
Why Should You Attend:
Reliability is the final proof of efficiency and efficacy of a product. During this training, you will discover why statistical reliability predictions rarely correlate with field performance, how to make big reductions in warranty costs, how to eliminate failures during early design, how to select proper tests for production screening, how to set up accelerated life tests, how to manage reliability growth, and how to predict the product life. Read more »
Online Event
Why Should You Attend:
The Theory of Lean Documents is the product of applying lean principles to the creation, design, process, and management of controlled documents typically found in regulated industries. Just as lean principles challenge traditional process concepts and “push” systems, many traditional document practices are artifacts of a flawed approach. Lean documents presents a fresh departure from these practices, while building upon proven principles. Lean configuration comes from the same principles, utilizing the unique power of software solutions to take over functions that had previously burdened controlled “paper” documents. Read more »
Online Event
Why Should You Attend:
Significant changes in statutory, regulatory and Agency policies relating to medical devices, generally and in vitro diagnostic products in particular are currently underway. Read more »
Online Event
Why Should You Attend: Is your organization making too many engineering changes? Would you like to prevent this waste of engineering resources and time?
The techniques discussed in this webinar will make you aware of the primary source of mistakes–the user requirements specifications. Read more »
Berjaya Hotel Manila
Makati City
FREE VIRTUAL SEMINAR IN MANILA
It’s a virtual world after all!
Potential virtual assistants will have the opportunity to take part in a free Virtual Staff Finder seminar this month here in Manila.
This virtual confab for enterprising virtual assistants will be held at the Berjaya Hotel Manila on September 10, 2011, Saturday from 1:00PM to 5:00PM. Read more »
Online Event
Palo Alto CA
This webinar will teach specific techniques to ensure your organizations are ready for regulatory inspections. We will focus on ideas that will help identify areas of improvement before the formal inspection occurs. Further, you will learn techniques that will enhance your effectiveness during the audit execution. Read more »
Online Event
Palo Alto CA
This training class describes the mechanics of a sound maintenance program from a ‘Quality’ perspective, including the major issues that are typically emphasized during regulatory audits. You will learn how to develop thorough maintenance documents that are clear and confusion-free. Additionally, you will discover how to perform and document corrective work in a manner that eliminates ambiguity and misunderstanding. Read more »
Online Event
Palo Alto CA
Why Should You Attend:
Reliability is the final proof of efficiency and efficacy of a product. During this training, you will discover why statistical reliability predictions rarely correlate with field performance, how to make big reductions in warranty costs, how to eliminate failures during early design, how to select proper tests for production screening, how to set up accelerated life tests, how to manage reliability growth, and how to predict the product life. Read more »