Technical Writer

As an experienced regulatory affairs and pharmacovigilance specialist, I bring a robust background in research and development, particularly in the cutting-edge fields of polymer drug delivery and nanotechnologies.

• DIN EN ISO 13485
• ICH guidelines
• ISO14971 and 21CFr
• Medical devices
• Medizinischer Kodierer
• Pharmacovigilance
• pölymer drug delivery and nanotechnology
• Quality associate
• Regulatory Affairs
• Wissensbilanzen

My expertise lies in meticulously preparing and reviewing regulatory documents to ensure strict adherence to industry standards. I am a driven and detail-oriented professional with a passionate commitment to delivering sustainable healthcare solutions.