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2018 Healthcare Block-a-thon
ACT-IAC is planning a “Shark Tank” event focused on the viability of solutions that use Blockchain technology in addressing potential healthcare agency use cases (needs). Potential blockchain use cases have been pre-vetted by a variety of health sector participants from the ACT-IAC Blockchain Working Group, government representatives from HHS and its Operating Divisions (OPDIVs), the VA and DHA.Our health agency participants, alo...
November 8, 2018
Organizer: ACT-IAC
Location: Washington, DC
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Clinical and Medical Case Reports Conference
After the successful completion of Case Reports Annual Conference, which held at San Francisco in 2017, we take the opportunity to once again welcome you to Toronto, Canada from August 31, 2018 to September 01, 2018 for the 10th International Conference on Clinical and Medical Case Reports (Case Reports 2018). This lively congress will highlight interesting, informative and instructional case reports from all clinical disciplines. Case Reports...
August 31 - September 1, 2018
Organizer: ConferencesSeries Ltd
Location: Toronto, CA
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FDA General Principles of Software Vali...
Course "FDA's Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Software's level of complexity and use is expanding at exponential levels. Likewise, the potential risks to health follow suit. Ransomeware attacks hold your software hostage until you pay hundreds or thousands of do...
January 18-19, 2018
Organizer: GlobalCompliancePanel
Location: San Diego, CA
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Root Cause Analysis and CAPA using 8-D...
Errors and defects are a problem in virtually every industry. The goal of defect-free/error-free product or service delivery is the aim of every company. However, in order to eliminate defects or errors permanently, you must use a disciplined approach in order to ensure that the problem does not recur. One of the most widely-used tools is the 8 Disciplines (8D) methodology. 8D requires you to identify and fix the problem immediately (put a ban...
August 24-25, 2017
Organizer: GlobalCompliancePanel
Location: Bloomington, MN
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FDA Scrutiny of Promotion and Advertisi...
If you go "off label" with advertising and promotion, FDA's hammer can hit hard and seemingly out of the blue. Advertising and promotion for devices is weak and lacks legal clarity. For drugs, the regulations are prescriptive and guidance documents clamp down on nuances. Marketing and regulatory affairs departments must collaborate to avoid the hammer and penalties of FDA. The roadblock, however is that marketing managers and regulatory affair...
August 24-25, 2017
Organizer: GlobalCompliancePanel
Location: Bloomington, MN
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Lineament analysis and appropriate samp...
Upon completing this course, participants should: Understand the limitations of the current exploration process Learn to use lineament and satellite interpretation as a way to define where to concentrate their exploration efforts How to implement QA&QC procedures to guarantee the quality of the collected data Why you should attend: We will introduce you to an effective and affordable methodology that identifies prospective targets which ar...
August 24-25, 2017
Organizer: GlobalCompliancePanel
Location: Hebron, KY
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Quality Management System ISO 13485- 2017
The final version of ISO 13485:2016 is now available and companies should be planning their implementation. There are significant changes from the earlier version; they will require major modifications to the Quality Management System (QMS). The new version has better alignment with FDA's QSR, but there are still major differences that create issues for effective QMS implementation. This workshop covers the differences from the 2003 version to...
August 17-18, 2017
Organizer: GlobalCompliancePanel
Location: Schiller Park, IL
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New FDA FSMA Rules on the Sanitary Tran...
Transportation and Logistics food transportation food safety rules are currently being finalized by the U.S. Food and Drug Administration (FDA). Under congressional instructions, the Food Safety Modernization Act (FSMA) requires the FDA to establish rules to improve, audit and enforce new food transportation rules. The rules provide a significant focus on foods not completely enclosed by a container, risk reducing adulteration prevention, pers...
August 17-18, 2017
Organizer: GlobalCompliancePanel
Location: Morrisville, NC
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Documenting Software for FDA Submissions 2017
When medical device companies consider Agile development methods, they often run into the key criticism that Agile groups produce little to no documentation, and that Agile stands in contradiction to the lifecycle standards outlined in IEC 62304. In fact, those principles - have clear processes for quality management system, risk management process, software maintenance, configuration management, and problem resolution - actually augment rathe...
August 10-11, 2017
Organizer: GlobalCompliancePanel
Location: Arlington, VA
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Statistical Methods A Visual Approach 2017
An essential task in any compliance analytics workflow is to not only explore your data visually, but also to communicate your results professionally with graphic displays. Do you have the tools and skills to quickly and thoroughly perform these tasks? This course in data visualization will present methods to allow you to interactively discover relationships graphically. We will provide the foundations for creating better graphical information...
August 3-4, 2017
Organizer: GlobalCompliancePanel
Location: Morrisville, NC
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