Medical Devices Translation Life Cycle II: To-Market and Post-Market Regulatory Requirements

Format: Webinar presentations
Topic: Medical translation

Course summary
Start time:Oct 20, 2017 13:00 GMT     Add to calendar

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If you could not participate in the webinar you can still get unlimited access to the webinar recordings and handouts. Purchase two on-demand sessions for only 50 USD 42 USD today!

See other sessions from the bundle below:

* On-demand training Medical Devices Translation Life Cycle I: Pre-Market and Regulatory Requirements

* On-demand training Medical Devices Translation Life Cycle II: To-Market and Post-Market Regulatory Requirements
Language:English
Description
Medical device translation not only requires expert medical and linguistic knowledge, but also an understanding of the strict industry standards and regulatory framework. In a sector that is undergoing constant technological advancements, even the definition of a “medical device” continues to expand – now even including software, in vitro reagents and tissue engineered medical products.


In part II of this presentation, we will delve into to-market translation materials, such as website content, internal and sales training materials (including e-learning) as well as manufacturing documentation and SOPs. Finally, we will address post-market requirements, including post-market clinical follow-up (PMCF) documentation field safety notices (FSN) and regulations on medical device disposal, recycling and waste prevention.



Training program:

- The to-market and post-market medical device lifecycles
- Internal vs. external communications and requirements
- Training materials for a digital world
- Understanding new waste, recycling and disposal requirements and language
- Translation resources
- Terminology strategies




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Target audience
Translators already specialising in medical translation.
Translators considering crossing over into medical translation.
Translators who want to learn more about translating for the medical devices sector.
Learning objectives
At the end of this session, participants will be able:

To identify the requirements for to-market translation materials.

To understand regulatory requirements and controlled languages for internal and external documentation.

To identify glossaries and language resources for translating post-market documentation..

To develop a system for managing controlled language and flagging regulatory requirements in TMs.

Prerequisites
No prerequisites.
Program
Click to expand
- The to-market and post-market medical device lifecycles
- Internal vs. external communications and requirements
- Training materials for a digital world
- Understanding new waste, recycling and disposal requirements and language
- Translation resources
- Terminology strategies

Registration and payment information (click to expand)
Click to expand
To purchase your seat at this session please click on the "buy" button. Available slots are limited and will be assigned to registered and paid participants as soon as payment is reported. Early payment is advised in order to secure participation. Allow some time for payment processing if you are paying by wire transfer.

After your payment is received, your status will be changed to “registered and paid” and your spot for the session will be secured. An invoice and receipt of payment will be sent to you for your records.

How do I access the online platform?

72 hours before the webinar takes place, you will receive an invitation to join the session. Please, click the registration link or button provided in the invitation email and complete the registration form.
Virtual platform system requirements
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For PC-based Users:

• Required: Windows 7 – Windows 10
• Required: Google Chrome v39 or later; Mozilla Firefox v34 or later; Internet Explorer v8 or later (JavaScript™ and Java™ enabled)
• Required software: GoToWebinar desktop app; JavaScript enabled
• NOT required: Microphone - attendees can communicate with the trainer through incorporated chat.

• Internet Connection Required: 1 Mbps or better (broadband recommended)
• Recommended: 2GB or more of RAM (recommended)


For Mac®-based Users:

• Mac OS X 10.8 (Mountain Lion) – 10.11 (El Capitan)
• Required: Microsoft Edge; Apple Safari v6 or later
• Required software: GoToWebinar desktop app; JavaScript enabled
• NOT required: Microphone - attendees can communicate with the trainer through incorporated chat.

• Internet Connection Required: 1 Mbps or better (broadband recommended)
• Recommended: 2GB or more of RAM (recommended)

Join from Android

• Operating system: Android 4.0 (Ice Cream Sandwich) or later
• Internet connection: 3G connection or better (WiFi recommended for VoIP audio)
• Software: Free GoToWebinar App from the Google Play Store

Recommendations

• For the visual section of the training course, we recommend that you have a 64kbps link. This means using an ISDN line or Broadband. Wireless connection is NOT recommended.
• For the audio section of the training course, we recommend that you have a headset or speakers.
• We recommend that you log in 30 minutes in advance of the start time to prepare for the training course.

Courses will be open half an hour before the start time. Please login before the start time to ensure that everything on your system is working correctly.
Created by
 Erin Lyons    View feedback | View all courses
Bio: Erin M. Lyons is a full-time French to English and Italian to English translator, medical writer, and consultant and the Owner and President of BiomedNouvelle. Her primary areas of focus include clinical research, pharmaceuticals, medical devices, and cosmetic products and she has split her professional career between Europe and the U.S. She has a BA in Romance Languages and Literature from the University of Chicago and an MA in Italian and French Translation from the Monterey Institute of International Studies. She has presented at several ATA Annual Conferences, as well as at the 2011 World Congress of the International Federation of Translators and the 2013 ProZ.com International Conference (Porto) and 6th Annual Congress and Training in France (Biarritz).
General discussions on this training