
Mr. Ludwig Everaert
Trainer
Ludwig Everaert, has extensive experience in the pharmaceutical industry, having started in 1989 after earning degrees in Pharmaceutical Sciences and Marketing/Business Administration. He founded a successful consultancy in 1999, providing services in pharmaceutical market access, regulatory affairs, and commercial activities. The company had a quality system audited by customers and European health authorities, and had long-term service agreements with over 120 customers before being sold in 2021. Ludwig now offers training services in multiple fields through his company QSME, including clinical research, regulatory affairs, pharmacovigilance, and medical writing.
Reasons to attend If you want to advance your clinical project management skills in order to be mor...
Reasons to attend A good clinical study stands or falls with a good clinical study design & pro...
Reasons to attend This Keeping oversight of safety training program covers pharmacovigilance obliga...
Reasons to attend The Pharmacovigilance training will highlight the mandatory requirements for phar...
Regulatory Affairs - Training Programme Regulatory Affairs (RA) is essential to ensure that pharmac...
Reasons to attend If you are a clinical research professional, investigator, monitor or other staff...