Dr. Julian Bickel

Regulatory responsibility for non-sterile, non-measuring Class I medical devices. International regulatory support for markets including the UK, Switzerland, and Turkey. Artwork and labeling compliance, including claims assessment. Implementation of EU PPWR requirements. Quality management responsibilities include internal and supplier audits, certification management (e.g. ISO, IFS, BRCGS, Nordic Ecolabel), process documentation, document control, and HACCP.

- Development and optimization of analytical methods - Interdisciplinary and cross-departmental collaboration in clinical settings - Interpretation of toxicological findings considering pharmacokinetic parameters - Preparation of clinical reports - Conducting student seminars - Research on postmortem toxicokinetic

- Preparation of pharmaceutical formulations - Advising and assisting customers - Medication management

Promotion in forensischer Toxikologie (Note: 1.0, magna cum laude) - Entwicklung und Validierung von LC-MS/MS-Methoden zur Analyse postmortaler Proben - Eigenständige Forschung zu Pharmakokinetik und Substanzstabilität - Veröffentlichung mehrerer Artikel - Präsentationen auf Fachkongressen - interdisziplinäre Zusammenarbeit und Lehre im Bereich Pharmazie und Medizin.