High-standard scientific and marketing materials for different types of audience and on various therapy areas
Clinical regulatory writing – leadership of medical writing activities for US and EU regulatory submissions, including the redaction and anonymisation of documents according to EMA Policy 0070
Impactful presentations for all types of congress sessions, educational initiatives and winning pitches
Active member of the EMWA Budapest Working Group that developed the CORE (Clarity and Openness in Reporting: E3-based) Reference (www.core-reference.org)
Pharmaceutical regulatory writing – study protocols and reports including statistical experimental designs and findings, batch manufacturing records and standard operating procedures
Qualification and Validation of Equipment, Cleaning and Processes
Delivery of international meeting materials from the stages of programme development, to on-site and post-meeting resources
Professional indemnity
Professional indemnity