This webinar on IND and IDE Application management will help you understand the current FDA requirements for IND and IDE application post initial approval to proceed with the clinical trial.
This webinar on alarms in patient monitoring devices will show how you can address FDA concerns regarding alarm standards and safety.
Medical device firms need to be aware of the benefits of compliance as well as the dangers of inadequate complaint handling.
HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding Penalties - US Seminar 2012 at Boston
Learn and understand the rules for international terms of sale; save pages of contract information by use of the proper rule.
This 90-minute webinar on supplier controls will help you refine your supplier management and audits to match the FDA's tougher position.
By lowering the import risks to your suply chain would lead to fewer Customs inspections and delays to your freight. The reduce lead times would enhance cost savings.
Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
Short and quick overview of the Part 11 regulation; detailed description of HOW TO prepare for an FDA inspection when and where Part 11 is in scope or the scope of the inspection
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
Find out what HHS OCR is likely to ask you if you are selected for an audit, and what you'll have to have prepared already when they do.
This webinar will provide you with an overview of risk factors in clinical trials and discuss possible ways to mitigate, control, assess impact, and prevent them in your trial.
Statistics for the Non-Statistician - US Seminar 2012 at Washington DC
Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel
The subject of risk compliance and 'are you prepared' is being discussed far more frequently (using platforms like webinars and white-paper downloads)
The topic aims to address and compare the requirements of SOX against the Dodd-Frank legislation and contrast how they differ clearly in purpose and objectives.
This webinar on clinical trial audit/ inspection preparedness will discuss in detail about applicable regulatory and sponsor requirements, guidelines and SOPs.
Join experts in the fields of design, mobile, gaming, usability, strategy, content, multimedia, and film in Big D.
We will review the latest inspection statistics released from FDA, discuss how to prepare for an FDA Inspection,
This 90-minute webinar on device corrections and removals will clarify your obligations for corrections and removals under Part 806 of the FDA regulations.
This 90-minute presentation will cover the FDA Quality System Requirements for software used in medical devices.
This webinar will help you understand how non-IND clinical trials at non-US locations can be used successfully to support an IND/IDE or a marketing approval application.
This 90-minute presentation will discuss a structured way to mitigate risks with minimum cost. You will learn how to use FMEA to effectively estimate and assess risks in your medical device.
Current and future compliance professionals, lenders, loan originators, board of directors, senior management. Anyone responsible for the development, marketing, and sales of bank products .
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The Boxes and Arrows event calendar is a place to find events of interest to designers. These can be specific design events, such as an AIGA event, SXSW or the IA Summit, part design/part other, such as Webvisions or it can be tangentially related, such as a business event or one on CSS.
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