All fda Events (113)

Seminar on GMP Compliance for Pharmaceutical Quality Control Laboratories at Zurich, Switzerland

September 24, 2015 at 9am to September 25, 2015 at 6pm – Hilton Zurich Airport Overview: This course will present the regulations and guidelines that apply to operations in quality control testing laboratories. In some cases these will not be specific regulations, but needs tha… Organized by John Robinson | Type: food, fda, medical, device, defence, and, navy, aerospace, mining
2-day In-person Seminar on Marketing Products without Getting Hammered by FDA at Zurich, Switzerland

September 24, 2015 at 9am to September 25, 2015 at 6pm – Hilton Zurich Airport Overview With this seminar you will learn how to navigate FDA's legal requirements and its interpretations for enforcement purposes. The agency now applies the principles of cognitive psychology to a… Organized by John Robinson | Type: food, fda, medical, device, defence, and, navy, aerospace, mining
2-day In-person Seminar on Performing Data Analysis with Multiple Tools: Pandas, R and Deedle (F#/C#) at SFO, CA

September 24, 2015 at 9am to September 25, 2015 at 6pm – DoubleTree by Hilton Hotel San Francisco Airport Overview: The seminar will begin with an over view of data science and many the steps required for collecting, cleaning, organizing and deriving information out of data. The steps are common to all o… Organized by John Robinson | Type: food, fda, medical, device, defence, and, navy, aerospace, mining

2-day In-person Seminar on Compliance Software Solutions for Medical Devices at Singapore

September 28, 2015 at 9am to September 29, 2015 at 6pm – Mandarin Orchard Singapore Overview: Software's level of complexity and use is expanding at exponential levels. Likewise the potential risks to health follow suit. Problems with software create a number of different hurdles. S… Organized by John Robinson | Type: food, fda, medical, device, defence, and, navy, aerospace, mining

Seminar on Validation and Part 11 Compliance of Computer Systems and Data at Mumbai

April 28, 2016 at 9am to April 29, 2016 at 6pm – The LaLiT Mumbai Overview: This 2-day course provides the regulatory background and guides attendees through the complete equipment qualification, calibration and computer system validation processes from planning to… Organized by John Robinson | Type: seminar, pharma, medical, fda, validation, complaince

Why is FDA at my facility, and what do I do during an inspection 2017

April 6, 2017 at 9am to April 7, 2017 at 6pm – Baltimore, MD Course "Why is FDA at my facility, and what do I do during an inspection" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completi… Organized by NetZealous DBA as GlobalCompliancePanel | Type: why, is, fda, at, my, facility, and, what, do, i, during, an, inspection, 2017

New FDA FSMA Rules and Food Safety Controls 2017

April 13, 2017 at 9am to April 14, 2017 at 6pm – Baltimore, MD Course "Preparing to Comply with the New FDA FSMA Rules: Planning Valid Preventive Food Safety Controls" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC re… Organized by NetZealous DBA as GlobalCompliancePanel | Type: new, fda, fsma, rules, and, food, safety, controls, 2017

Overview of Device Regulation – FDA 2017

April 20, 2017 at 8:30am to April 21, 2017 at 5:30pm – San Diego, CA Overview: This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers gui… Organized by NetZealous DBA as GlobalCompliancePanel | Type: overview, of, device, regulation, –, fda, 2017
Applied Statistics for FDA Process Validation 2017

April 20, 2017 at 9am to April 21, 2017 at 6pm – San Diego, CA Course "Applied Statistics for FDA Process Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: In… Organized by NetZealous DBA as GlobalCompliancePanel | Type: applied, statistics, for, fda, process, validation, 2017

Preparing Premarket Submissions that secures U.S. FDA Clearances/Approvals 2017

April 27, 2017 at 9am to April 28, 2017 at 6pm – San Diego, CA Overview: This workshop style training course is designed based on 30 year of regulatory affairs experience in preparing more than 150 successful U.S. FDA submissions for major medical device compan… Organized by NetZealous DBA as GlobalCompliancePanel | Type: preparing, premarket, submissions, that, secures, u.s., fda, clearances/approvals, 2017