Expertise

Indikationen (Auswahl)

 Allergologie

 Immunologie (Vakzine)

 Kardiologie

 Medizinprodukte

 Nahrungsergänzungsmittel

 Onkologie

 Orthopädie

 Pädiatrie

 Phytopharmaka

 Urologie

Ästhetische Medizin

Aktuelle EU Regulations und Gesetze im Arzneimittel- und Medizinproduktebereich, GCP-Training

Medical Writing Workshops der European Medical Writers Association

Seit 2018: Mitglied der American Medical Writers Association

Seit 2015: Mitglied der European Medical Writers Association

WS: Introduction to Combination Products in the US and EU

WS: How to Handle Advisory Board Meetings

WS: Introduction in Pharmacokinetics

WS: Post-Market Clinical Follow-Up for Medical Devices

Workshop: PM – Do more with less, faster

Workshop: Scheduling & proposal writing: The clinical study protocol & report

Workshop: Publication Planning

WS: Clinical Study Reports in Oncology

WS: Writing a Clinical Evaluations Plan for Medical Devices

WS: Graphical Abstracts

WS: Medical Writing for Biosimilars

WS: Understanding Instructions for Use of Medical Devices and Providing Support in Their Drafting

WS: Writing Clinical Investigation Plans for Medical Devices

WS: Statistical Analysis of Binary Data

WS: Writing a Clinical Study Protocol

WS: Manuscript Writing - from Good to Excellent

WS: Writing Lay Summaries of Study Results according to EU Regulations

WS: Literature Reviews for Medical Devices

WS: Introduction to Virology

WS: Advanced Epidemiology

WS: Statistical Testing

WS: Critical Appraisal of Medical Literature

WS: Subject narratives for clinical study reports

WS: Going from Pharma to Medical Devices

WS: Writing Clinical Evaluations Reports of Medical Devices

WS: Strategies for Improving Document Quality

WS: Medical Writing and Quality Control of Documents Entering the Public Domain: Manuscripts and Abstracts

WS: Summarizing

WS: Basics of Writing for Medical Devices Under the MEDDEV rev. 4 and new Medical Devices Regulations

WS: Drug Safety for Medical Writers Part 1: Adverse Events and Concomitant Medications

WS: Drug Safety for Medical Writers Part 2: Laboratory Data

WS: Basics of Epidemiology for Medical Communicators

WS: Medical Writing and Quality Control: CSRs

WS: Writing Global Submission Dossiers using the Common Technical Document

WS: Health Related Quality of Life

WS: From Clinical Study Report to Manuscript

WS: CORE Reference – Clarity and Openness in Reporting: E3-based

WS: Introduction to Writing about Efficacy

WS: Medical Writing and Observational Studies

WS: Patient Registries as a Source of Medical Information

WS: The Investigator’s Brochure

WS: Managing the Clinical Study Protocol Writing Process

und weitere Webinare zu Themen des Medical und Scientific Writings

WS: Workshop