About

About


Welcome to NACHTIGAL SERVICES – your officially authorized and certified translator for English, German, and Russian. We specialize in certified document translations for authorities, courts, consulates, and private clients, with a particular focus on USCIS immigration applications for the United States. Be it a birth certificate, marriage certificate, divorce decree, police clearance, or academic transcript, we provide translations that include the required USCIS certification: complete, accurate, and signed, so your documents are ready for submission.

In addition to legal and immigration documents, we also offer technical translations in the field of medical devices, combining linguistic expertise with highest accuracy. Whether certificates, technical documentation, instructions for use (IFUs) or clinical evaluation reports - your texts are in expert hands. As an authorized translator from the Higher Regional Court of Hamm, as well as a quality management representative (QMB) and responsible person in accordance with Article 15 of the MDR (EU) 2017/745, I can support you with everything that is linguistically necessary for approvals, registrations or audits.

Peter Nachtigal – Übersetzer für Russisch, Deutsch und Englisch bei Nachtigal Services

English-German-Russian

According to § 34 of the JustG NRW (Judicial Act of the State of North Rhine-Westphalia), I am authorized to certify the accuracy and completeness of translations. I translate official certificates and documents intended for submission to authorities, embassies, consulates, or employers – typically within 24 hours – and deliver them both digitally as a PDF and in printed form.

"To always offer you the highest quality and professional expertise, I regularly continue my education – because every training is an investment in even better results."

2025

  • Certified Translator (English)

2024

  • German Legal Terminology
  • Risk Management according to EN ISO 14971
  • Usability Engineering for Medical Devices (EN 62366-1)
  • Technical Documentation for Medical Devices in accordance with Regulation (EU) 2017/745

2023

  • Monitoring and Management of Measuring Equipment in accordance with ISO 13485
  • Economic Operators under the MDR (EU) 2017/745 and IVDR (EU) 2017/746

2022

  • Introduction to the Legal System under the MDR

2021

  • MDR Requirements in QMS
  • Product Information Requirements for Medical Devices (MPDG, HWG)
  • Outsourcing Processes in the Medical Device Industry
  • Data Protection and the GDPR
  • UDI (Unique Device Identification) for Medical Devices

2020

  • Biological and Toxicological Evaluation of Medical Devices (ISO 10993-series)
  • Fundamentals of Professional Communication
  • Transport and Shipment of Lithium Batteries – Classification and Categorization

2019

  • Development of Medical Software in accordance with EN 62304
  • Person Responsible for Regulatory Compliance (PRRC) under Article 15 of Regulation (EU) 2017/745
  • Overview of Regulation (EU) 2017/745

2018

  • Post-Market Surveillance of Medical Devices
  • Medical Device Regulation (MDR)

2017

  • EN 60601-1 – General Requirements for Basic Safety and Essential Performance of Medical Electrical Equipment
  • Clinical Evaluation and Investigation of Medical Devices (MEDDEV 2.7/1 rev. 4)
  • OEM and ODM Partnerships in the Medical Device Sector
  • ISO 13485:2016 – Quality Management Systems for Medical Devices

2016

  • Fundamentals of Medicine
  • Quality Management in accordance with EN ISO 13485

2014

  • Safety Officer in accordance with § 30 of the German Medical Devices Act (MPG)

2013

  • Customer-Focused Communication
  • Healthcare Management

2012

  • Requirements for Technical Documentation for Medical Devices and IVDs
  • Risk Management in accordance with EN ISO 14971

2011

  • ISO 13485 – Quality Management Systems for Medical Devices

2008

  • Bachelor of Science in Economics (Major and Minor)

2004

  • Certified Foreign Language Correspondent – English