2-day In-person Seminar: Computer System Validation - Reduce Costs and Avoid 483s
By : Compliance online
Description : This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments.
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United States US
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San Francisco
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02 Feb 12
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03 Feb 12
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International Conference on Biomedical Electronics and Devices (BIODEVICES 2012)
By : INSTICC
Description : This conference will bring together researchers and practitioners from electronics and mechanical engineering, interested in studying and using models, equipments and materials inspired from biological systems and/or addressing biological requirements.
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Portugal
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Vilamoura, Algarve
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01 Feb 12
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04 Feb 12
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Clear as Mud: Obtaining and Marketing Your 510(k) With Today's FDA
By : Compliance online
Description : When you get your 510(k) how to market your 510(k) , what communication strategy to adopt, what to do when FDA disagrees with your promotional positioning.
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United States US
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Salt Lake City, Utah
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27 Jan 12
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27 Jan 12
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Understanding and Implementing the Medical Device Directive
By : Compliance online
Description : This interactive two-day course will help you comprehensively understand details of the MDD and implement its requirements. Attendees will learn how to classify devices, select the appropriate conformity assessment path, prepare the required documentation, and maintain it.
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United States US
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San Diego
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26 Jan 12
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27 Jan 12
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Migrating to Oracle Argus Safety
By : BioPharm Systems
Description : Leading software implementation and migration experts will discuss how to successfully approach an Oracle Argus Safety migration project.
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United States US
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Virtual
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25 Jan 12
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25 Jan 12
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Application of CAPA in (Device) Sterilization – For the Non-Expert
By : Compliance online
Description : This webinar will review the typical non-conformances experienced in the (Medical Device) sterilization process and the course of action that should be taken by the manufacturer or contract sterilizer.
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United States US
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Palo Alto
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20 Jan 12
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20 Jan 12
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SOPs for Clinical Trials – Regulatory Requirement and Key to Effective Management
By : Compliance online
Description : This SOPs for Clinical Trials training will cover ICH-GCP and ISO 14155 requirements for SOPs. It will outline steps to effectively develop and maintain SOPs and manage risks to your clnical research operation, through their use.
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United States US
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Palo Alto
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19 Jan 12
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19 Jan 12
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Supplier Evaluation and Assessment - FDA QSR and ISO 13485 Requirements
By : Compliance online
Description : Detailed review the QSR and ISO requirements for supplier evaluation and assessment, and cost efficient options to many of the common practices.
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United States US
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Palo Alto
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19 Jan 12
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19 Jan 12
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Production and QMS Software Validation - An Excel Example
By : Compliance online
Description : This webinar covers production and QMS requirements for software (Excel spreadsheet) built into a medical device, as outlined in 21 CFR 820.70(i). Get practical advice on writing validation protocols and reports for Excel spreadsheets.
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United States US
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Palo Alto
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18 Jan 12
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18 Jan 12
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How to Format a Succinct and Comprehensive 510(k) Submission
By : Compliance online
Description : This 90-minute 510(k) webinar will discuss the recent changes in the 510(k) program and will walk you through how to better format a 510(k) premarket notification submission to increase submission quality and to proactively facilitate the review process in a streamlined manner.
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United States US
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Palo Alto
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17 Jan 12
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17 Jan 12
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Clinically-Related 483's and Warning Letters: Getting through the Maze - Webinar By ComplianceOn
By : Compliance online
Description : This webinar on Clinically-Related 483's and Warning Letters will show how you can manage clinical site FDA inspections, handle issues, understand and respond to observations ("483") and/or Warning Letters.
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United States US
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Palo Alto
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08 Dec 11
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08 Dec 11
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FutureHealth Forum Malaysia 2011
By : Alphabet Media
Description : Transform – Manage – Deliver. This Forum will tackle how Malaysia will handle the rapidly changing environment of healthcare to deliver its local and international patients’ expectations.
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Malaysia
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Kuala Lumpur
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07 Dec 11
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07 Dec 11
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