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Dec 4 @ 4:00 PM – 5:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar Risk Management for Medical Devices and IVDs: Systematic and Holistic Approaches Date: June 6, 2017 NOTE: This LIVE seminar recurrs bi-monthly (every other month) on 1st Tuesdays. Your payment would apply for the next upcoming LIVE online seminar unless indicated
Dec 5 @ 3:00 PM – 4:00 PM
LIVE Online Seminar FDA Pre-submission and 510(k); Best Practices Date: November 2, 2016 NOTE: This 510(k) LIVE seminar recurrs monthly on 1st Wednesdays. Time: 12:00 PM PST | 03:00 PM EST Duration: 60 Minutes. About the Seminar This presentation will walk you
Dec 10 @ 11:00 AM – 12:00 PM Online
LIVE Seminar Online Overview of the EMA Marketing Authorization Applications (MAAs) for Medicinal Products for Human Use in EU Date: December 11, 2017 or email us to schedule a date and time NOTE: This seminar recurrs tri-monthly (every three month) on
Dec 10 @ 1:00 PM – 2:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar Quality Risk Management for Drugs and Biologics: Systematic and Holistic Approaches Date: June 12, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 2nd Mondays. Time: 12:00 PM PST | 03:00 PM EST Duration: 60 Minutes About the
Dec 10 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Dec 10 @ 2:00 PM – 3:00 PM LIVE Online
LIVE Online Seminar PMA Drafting Seminars Date: Starting on April 9, 2018 NOTE: This seminar recurrs bi-monthly (every other month) February, April, June, August, October and December Time: 2nd Mondays at 11:00 AM EST OR 2:00 PM EST OR by scheduling at your
Dec 11 @ 4:00 PM – 5:00 PM LIVE Online
LIVE Online Seminar Learning LIVE How To Draft a 510(k) Like a PRO Date: recommended to contact us to schedule the 510(k) seminar (online) NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next
Dec 11 @ 1:00 PM – 2:00 PM Your Computer (Online)
LIVE Online Seminar Establishing an FDA-Compliant UDI System Date: June 13, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 2nd Tuesdays. Your payment will apply for the next upcoming LIVE online seminar unless requested otherwise after registration. Time: 10:00 AM
Dec 11 @ 3:00 PM – 4:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar CE Mark: Content and Format for a Technical File and Design Dossier Date: June 13, 2017 NOTE: This seminar recurrs tri-monthly (every 3 month) on 2nd Tuesdays. Your payment will apply for the next upcoming LIVE online seminar unless requested
Dec 12 @ 4:00 PM – 5:00 PM LIVE Online Seminar
LIVE Seminar Online Demystifying Design Control: Design History File (DHF), Device History Record (DHR), and Device Master Record (DMR) Date: June 14, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 2nd Wednesdays. Your payment will apply for the
Dec 13 @ 11:00 AM – 12:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar Best Practices for Communicating and Interacting with FDA Reviewers Date: December 8, 2016 This seminar recurs tri-monthly on second Thursdays. Time: 08:00 AM PST | 11:00 AM EST Duration: 60 Minutes About the Seminar This seminar (webinar) is intended to
Dec 13 @ 3:00 PM – 4:00 PM Your Computer (Online)
LIVE Online Seminar Implementing Medical Device Complaint Handling Systems Date: April 13, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Thursdays. Your payment will apply for the next upcoming LIVE online seminar unless requested otherwise after registration. Time: 12:00
Dec 13 @ 4:00 PM – 5:00 PM LIVE Online
LIVE Online Seminar Title: Complaint Handling and Medical Device Reporting (MDR) Date: December 8, 2016 This seminar recurs tri-monthly on second Thursdays. Time: 01:00 PM PST | 04:00 PM EST Duration: 60 Minutes About the Seminar As a domestic or foreign medical device manufacturer
Dec 14 @ 11:00 AM – 12:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar Medical Device Laws and Regulations in Asian Countries: China, Hong Kong, Japan and Korea Date:  June 9, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 2nd Fridays. Your payment will apply for the next upcoming LIVE online seminar
Dec 14 @ 12:00 PM – 1:30 PM Online
LIVE Online Seminar How to Most Effectively Prepare for the US RAC Exam Date: April 13, 2018 Time: 09:00 AM PST | 12:00 PM EST Duration: 90 Minutes About the Seminar Having a credential for Regulatory Affairs Certification (RAC) can
Dec 14 @ 1:00 PM – 2:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar Establishing FDA-Compliant Social Media Practices to Avoid FDA Actions Date: December 9, 2016 NOTE: This seminar recurrs bi-monthly on second Fridays. Time: 09:00 AM PST | 12:00 PM EST Duration: 60 Minutes. About the Seminar This seminar is intended to
Dec 14 @ 2:00 PM – 3:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar FDA 510(k): Preparation, Submission, and Clearance Date: November 11, 2016 NOTE: This 510(k) LIVE seminar recurrs monthly on 2nd Fridays. Your payment would apply for the next upcoming LIVE online seminar unless indicated otherwise after registration. Time: 11:00 AM
Dec 14 @ 4:00 PM – 5:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar Developing and Implementing a Global Regulatory Plan and Strategy Date: April 13, 2018 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Fridays. Your payment will apply for the next upcoming LIVE online seminar unless requested otherwise after registration.
Dec 17 @ 11:00 AM – 12:00 PM Your Computer (Online)
LIVE Online Seminar  Big Data in FDA-Regulated Healthcare Industry: Best Practices for Systematic Use Date: December 19, 2016 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Mondays. Your payment will apply for the next upcoming LIVE online seminar unless requested
Dec 18 @ 3:00 PM – 4:00 PM Your Office (Online)
LIVE Online Seminar Implementing Compliance Requirements for Social Media Marketing Ads and Promotional Videos Date: February 16, 2016 NOTE: This seminar recurrs bi-monthly on third Tuesdays. Time: 12:00 PM PST | 03:00 PM EST Duration: 60 Minutes. About the Seminar This seminar is
Dec 20 @ 3:00 PM – 4:00 PM Your Computer (Online)
LIVE Seminar Online FDA 510(k) Requirements, Submission, and Clearance: Best Practices Date: June 15, 2017 NOTE: This 510(k) LIVE seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment would apply for the next upcoming LIVE online seminar unless indicated otherwise
Dec 20 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Dec 21 @ 1:00 PM – 2:00 PM Online
LIVE Online Seminar Understanding ANDAs and Paragraph IV Patent Certifications Date: December 9 , 2016 Time: 10:00 AM PST | 01:00 PM EST Duration: 60 Minutes About the Seminar The regulatory requirements for generic drugs include, but not limited to,
Jan 1 @ 4:00 PM – 5:00 PM Online
LIVE Online Seminar Understanding Pain Management and Opioids: FDA Regulations, Generics and Recent Approvals Date: April 3, 2018 NOTE: This seminar recurrs tri-monthly (every three month) on 1st Tuesdays. Your payment will apply for the next upcoming LIVE online seminar unless requested otherwise
Jan 2 @ 3:00 PM – 4:00 PM
LIVE Online Seminar FDA Pre-submission and 510(k); Best Practices Date: November 2, 2016 NOTE: This 510(k) LIVE seminar recurrs monthly on 1st Wednesdays. Time: 12:00 PM PST | 03:00 PM EST Duration: 60 Minutes. About the Seminar This presentation will walk you
Jan 7 @ 1:00 PM – 2:00 PM Online
Two LIVE Online Programs in Regulatory Affairs The Fundamentals of Regulatory Affairs for Drugs (“Drug Program“) and Medical Devices (“Device Program“) Course Description Each class consists of 60-minutes of online seminar (LIVE or recorded) There are four classes for each program.
Jan 7 @ 2:00 PM – 3:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Seminar Online Implementing Global Medical Device Adverse Event Reporting (AER) Systems in EU, Canada and US Date: July 10, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Jan 11 @ 2:00 PM – 3:00 PM LIVE Online Seminar (LIVE Webinar)
LIVE Online Seminar FDA 510(k): Preparation, Submission, and Clearance Date: November 11, 2016 NOTE: This 510(k) LIVE seminar recurrs monthly on 2nd Fridays. Your payment would apply for the next upcoming LIVE online seminar unless indicated otherwise after registration. Time: 11:00 AM
Jan 25 @ 2:00 PM – 3:00 PM Global Compliance Seminar
LIVE Online Seminar Developing and Implementing an Effective SOP in Healthcare Industry Date: January 27, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 4th Fridays. Your payment will apply for the next upcoming LIVE online seminar unless requested otherwise after
Feb 4 @ 1:00 PM – 2:00 PM Global Compliance Seminar (Online)
LIVE Online Seminar Programs in Regulatory Affairs The Fundamentals of Regulatory Affairs in Medical Devices (“Device Program”) Course Description Each class consists of 60-minutes of online seminar (LIVE or recorded) There are four classes for each program. The Drug Program