MDPharmaCourses.com
0

No products in the basket.

ON DEMAND TRAINING FOR INDIVIDUAL OR SMALL TEAM

Pre-reserve your seat free and withour any charge (no payment required).

Latest Events

31 Oct

Training New MDR Regulation 2017/745 on Medical Devices: technical file structure

24 Jan

Live Webinar: Drafting of the Biocompatibility report in accordance with ISO 10993-1

13 Dec

Live Webinar Validation of industrial processes (IQ/OQ/PQ) and technology transfer in accordance with ISO 13485: 2016

Cart

Product tags

2017/745 biocompatibility biocompatibility webinar biological evaluation biological safety capa clinical evaluation Complaint form corrective action course DESIGN CONTROL design input design output design validation design verification emdr FDA fda training form iso 10993 ISO 13485 live webinar meddev meddev 2.7.1 medical device medical device training new mdr new medical device regulation preventive action quality system management regulatory regulatory affairs regulatory course tech file technical file template training udi udi training udi webinar Unique Device Identification unique device identification webinar VALIDATION warning letter webinar

ON DEMAND LEARNING FOR INDIVIDUAL OR SMALL GROUP

If You missed one of our live Webinar Events or you need support and additional guidance on a specific topic we can organize a 1 to 1 learning program for You or Your team. Learn More..

For any additional infomation reach out to us:

info@tsquality.ch

Contact Form

Cooperation Opportunities for SME

cooperation

Free Regulatory Resources

Here you can find a free and organic collection of Regulatory and Quality guidelines. cooperation

From MDadmin

MDPharmaCourses | Regulatory, Quality and Compliance Training
Regulation 745/2017 on Medical Devices: technical file structure – Live Webinar
MDPharmaCourses | Regulatory, Quality and Compliance Training
Regulation 745/2017 on Medical Devices: Unique Device Identification
MDPharmaCourses | Regulatory, Quality and Compliance Training
Live Webinar: Regulation 745/2017 on Medical Devices: post market activities and follow up
MDPharmaCourses | Regulatory, Quality and Compliance Training
Regulation 745/2017 on Medical Devices: main changes and timeline to implementation

Contact Info

+41 076 6405728

info@tsquality.ch

Derendingen (CH)

Basket

Stay Updated!

error: Content is protected !!