Skip to content
seleon GmbHseleon GmbH
  • info@seleon.com
  • +49 7131 2774-0
  • Contact us
  • About us
    • Vision / Mission
    • Company History
    • Team
    • Partners and Network
    • Downloads
  • Services
    • Development
      • Project Management
      • System Development
      • Electronics
      • Software / Firmware
      • Mechanics / Mechatronics
      • Documentation / Testing
    • Consulting
      • QM Consulting
      • Legal Manufacturer
      • Admissions Consulting
      • Process Consulting
      • Clinical Approval – CRO
    • Production
      • Supply Chain Managememt
      • Medical Technology Production
      • Special Systems
      • Manufacturing Equipment
      • Quality Management
  • Projects
  • Events
  • News
  • Career
  • Contact
  • Regulatory Affairs Blog
  • English
  • German
Regulatory Affairs Blog

Category: Lifecycle Processes

seleon GmbH > Lifecycle Processes
Frau - Megafon
30 Mar, 2020
Lifecycle Processes, Regulatory Affairs

Helping and doing the right thing – We show how protective products become regulatory clean

by seleon
Rote Flagge - Frau
24 Mar, 2020
Lifecycle Processes, Regulatory Affairs

Help in the Corona crisis – we support the manufacturers of protective masks and clothing

by seleon
Gelbe Enten - Hai
17 Mar, 2020
Lifecycle Processes, Regulatory Affairs

Risk management according to ISO 14971:2019 – what’s new?

by seleon
17 Feb, 2020
Lifecycle Processes, Regulatory Affairs

UDI – the countdown begins

by seleon
Weihnachtsman - Schnee
20 Dec, 2019
Clinical Affairs, Health Software, Lifecycle Processes, Regulatory Affairs

Corrigendum II MDR

by seleon
Frauen - Lesen
05 Dec, 2019
Clinical Affairs, Health Software, Lifecycle Processes, Regulatory Affairs

MEDDEV is going, MDCG is coming – an update of the guidance documents

by seleon
Löffel
29 Aug, 2019
Lifecycle Processes, Regulatory Affairs

Harmonized standards under the MDR

by seleon
MDSAP - Führung
01 Jul, 2019
Lifecycle Processes, Regulatory Affairs

You want to go to Canada? Only with MDSAP audit!

by seleon
Augen
06 Jun, 2019
Lifecycle Processes, Regulatory Affairs

Long live the SIBA

by seleon
Kind
04 Apr, 2019
Lifecycle Processes, Regulatory Affairs

MDR legal acts Part 2: Implementing acts

by seleon
1 2 3 4 5

Blog Search

Newest Articles

  • Artificial Intelligence Basics for medical technology 20. December 2022
  • Testing for cytotoxicity: The “well-established” EN ISO 10993-5 21. October 2022
  • Cleanliness of medical devices 28. September 2022
  • eIFU-Pflicht-seleon Electronic instructions for use – The hidden duty of MDR 17. August 2022

Kategorien

Fabiola Hartung-Linz
SALES DIRECTOR CONSULTING
Tel.: +49 7131 2774 - 40
Email: regulatoryaffairs@seleon.com
seleon GmbH
Any Questions? +49 7131 2774-0
seleon gmbh
Im Zukunftspark 9
74076 Heilbronn

More Information

  • Home
  • Vision / Mission
  • Services
  • Projects
  • Downloads
  • Contact

Memberships

Copyright © 2023 seleon GmbH, All Rights Reserved.

  • Legal Notice
  • Data Privacy Policy
  • General Business Terms