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Home page | Regulation StationRegulation station provides online training courses and webinars for medical device and diagnostic regulatory professionals and executives
http://www.regulation-station.com/
Regulation station provides online training courses and webinars for medical device and diagnostic regulatory professionals and executives
http://www.regulation-station.com/
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Home page | Regulation Station | regulation-station.com Reviews
https://regulation-station.com
Regulation station provides online training courses and webinars for medical device and diagnostic regulatory professionals and executives
regulation-station.com
Archived | Regulation Station
http://www.regulation-station.com/category/webinars/archived
Contact Us – 312.224.1693. Best Practices for Medical Device Reporting (MDR) Under FDA’s Final Guidance. 1 Hour Video Pamela F. Forrest and Scott D. Danzis, Covington and Burling LLP. Status Update- MDR Surprises and Key Regulatory Developments. 1 Hour and 30 Minute Video Erik Vollebregt, Axon Lawyers. How to Decide When a Modified Device Requires a 510(K) Clearance under New FDA Draft Guidances. 1 Hour Video Lynette Zentgraft and Elaine Tseng, King and Spalding. 1 Hour Video Val Surgenor, MacRoberts LLP.
Join Our Mailing List | Regulation Station
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Contact Us – 312.224.1693. Join Our Mailing List. Join our mailing list for the latest updates to current regulations, guidances, and information about our webinars and training courses. We Guarantee 100% Privacy, Your Information Will Not Be Shared. Prove you are human:. Contact Us 312.224.1693. Designed by Elegant Themes.
Diagnostic | Regulation Station
http://www.regulation-station.com/category/webinars/diagnostics
Contact Us – 312.224.1693. French Transparency Regulations: An Overview for the Life Science Industry. Presented By Baker and McKenzie SCP. Understanding Electronic Labeling Requirements for EU Medical Devices. Sunshine-Readiness: Key Considerations when Implementing an Aggregate Spend System. Presented By The Spectranetics Corporation and Life Compliance Solutions. Utilizing GS1 Standards to Implement and Comply with FDA UDI Requirements. FDA Final Guidance for Mobile Medical Apps. Presented By RPCS, LLC.
Medical Device | Regulation Station
http://www.regulation-station.com/category/webinars/medical-device
Contact Us – 312.224.1693. Deciphering Regulatory Guidance on Reusable Device Validation and Testing Methods. 1 Hour Video Paul Boentges, Becton Dickinson. FDA Draft Guidance: EAP Program & Premarket/Postmarket Data Collection for PMA’s. 1 Hour and 10 Minute Video Bethany J. Hills, Epstein Becker Green. The Latest Developments in Europe’s Regulation of Medical Devices and Projections for 2014. Presented By Axon Lawyers. French Transparency Regulations: An Overview for the Life Science Industry.
Global Regulations | Regulation Station
http://www.regulation-station.com/category/webinars/global-regulations
Contact Us – 312.224.1693. Sunshine-Readiness: Key Considerations when Implementing an Aggregate Spend System. Presented By The Spectranetics Corporation and Life Compliance Solutions. Utilizing GS1 Standards to Implement and Comply with FDA UDI Requirements. Pre- & Post- Market Adverse Event Reporting Requirements for European Device Trials. Presented By Applied Clinical Services. 2012 FDA Safety a. 2012 FDA Safety I. 21 CFR. Part 7. 21 CFR. Part 80. 21 CFR Part 50. 21 CFR Part 56. 21 CFR part 801.
TOTAL PAGES IN THIS WEBSITE
13
Pharmaceutical Webinar |
http://www.q1productions.com/category/webinars/pharmaceuticalwebinar
Pre- and Post- Market Adverse Event Reporting Requirements for European Device Trials. Analyzing the Complexities of IVD Clinical Sample Regulation in US Trials. Join Our Mailing List. Keep up on news and special offers from Q1. Expanded Access Update Developments at the FDA and Beyond. Expanded Access Update Developments at the FDA and Beyond. Thursday September 8, 2016 - 1:00PM to 2:00PM EDT. Development of a Single CMC Dossier for Tier 1 Countries to Streamline Submissions.
Device Webinar |
http://www.q1productions.com/category/webinars/devicewebinar
Pre- and Post- Market Adverse Event Reporting Requirements for European Device Trials. Analyzing the Complexities of IVD Clinical Sample Regulation in US Trials. Join Our Mailing List. Keep up on news and special offers from Q1. Practical Approaches for Managing Life Science Risks and Corruption in Asia. Practical Approaches for Managing Life Science Risks and Corruption in Asia. Wednesday September 14, 2016 10:00AM EDT to 11:00AM EDT. Clarification of the FDA Post-Market Guidance for Cybersecurity.
Diagnostic Webinar |
http://www.q1productions.com/category/webinars/diagnosticwebinars
Pre- and Post- Market Adverse Event Reporting Requirements for European Device Trials. Analyzing the Complexities of IVD Clinical Sample Regulation in US Trials. Join Our Mailing List. Keep up on news and special offers from Q1. Practical Approaches for Managing Life Science Risks and Corruption in Asia. Practical Approaches for Managing Life Science Risks and Corruption in Asia. Wednesday September 14, 2016 10:00AM EDT to 11:00AM EDT. Wednesday September 21, 2016 1:00PM EDT to 1:45PM EDT.
Webinars |
http://www.q1productions.com/category/webinars
Pre- and Post- Market Adverse Event Reporting Requirements for European Device Trials. Analyzing the Complexities of IVD Clinical Sample Regulation in US Trials. Join Our Mailing List. Keep up on news and special offers from Q1. Expanded Access Update Developments at the FDA and Beyond. Expanded Access Update Developments at the FDA and Beyond. Thursday September 8, 2016 - 1:00PM to 2:00PM EDT. Development of a Single CMC Dossier for Tier 1 Countries to Streamline Submissions. 500 N Dearborn, Suite 500 C...
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Regulation Matters ©
07890 657011 or 01748 833264 info@regulation-matters.co.uk. Please click the "Full screen" button above here to view the video. Care Industry Regulation and Compliance Consultancy. We can assist you with the Registration of a new Home. We can help with new registrations and variations and are able to assist and support homes facing regulatory challenges. Regulation Matters was formed by a care industry professional who has extensive knowledge of all relevant UK regulatory bodies.
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Home page | Regulation Station
Contact Us – 312.224.1693. Is the Leading Educational Portal for Regulatory Professionals Working in Medical Device and Diagnostics. Our Webinars Cover a Variety of Regulatory Challenges. Browse All of Our Upcoming Webinars by Industry, Region, or Regulation. We Have a Growing Archive of Presentations from Key Opinion Leaders in the Medical Device and Diagnostic Industries. Welcome to the Regulation Station, a division of Q1 Productions. Our goal is to address key regulatory challenges for the medical de...
Business & Regulation Summit
Banking and financial regulation. Speakers on TMT track. Speakers on Banking and Financial tracks. Speakers on Antitrust track. Business and Regulation Summit. REGULATORS: EXTRACT OF SPEAKERS. INTERNATIONAL COMPANIES: EXTRACT OF SPEAKERS. FINTECH COMPANIES: EXTRACT OF SPEAKERS. The second edition of the Business and Regulation Summit - event entirely dedicated to the regulation topic - took place at the Pavillon d’Armenonville,. Thursday, November 17, 2016. For more information, visit the.
Business & Regulation Summit
Programme des conférences 2015. Régulation Bancaire et Financière. Programme des conférences 2016. Intervenants tracks Banque and Finance. Un lieu d'exception. AUTORITÉS DE RÉGULATION : EXTRAIT DES INTERVENANTS. ENTREPRISES INTERNATIONALES : EXTRAIT DES INTERVENANTS. FINTECH : EXTRAIT DES INTERVENANTS. La seconde édition des Business and Regulation Summit. Cette journée de conférences exclusives fut suivie de la 2e édition des Trophées du Droit édition Entreprises. S'abonner à la newsletter.
TECHNOCEN - Accueil
TECHNOCEN : votre spécialiste en régulation de puissance . Fort d'une solide expérience dans notre secteur, nous sommes un partenaire compétent pour tout ce qui concerne la technique du régulation de puissance. Une régulation précise pour maîtriser les dépenses énergétiques. La régulation chronoproportionnelle de puissance est destinée à la régulation d’éléments résistifs chauffants. Les principales applications sont les installations de chauffage, traitement d’air et de climatisation :. Rendez-vous sur ...
Regulation Week
What is an Audio Conference? What Hot Topics or Speakers Would Interest You? How to Prepare for an OSHA Inspection. Brad Hammock, Partner, Jackson Lewis LLP. How to Prepare for an OSHA Inspection. Brad Hammock, Partner, Jackson Lewis LLP. New I-9 Form Compliance Overview: Industry Briefing. Julie R Pugh, Attorney, Graydon Head and Ritchey, LLP. EPA Enforcement Trends, Initiatives and Enforcement Tools/Methods. Andrew L. Fono, Shareholder, Winstead, LLC.
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