Training: build your team’s skills
I run initial and continuing training for everyone involved in clinical studies: investigators, CRAs, study coordinators, nurses and pharmacists. Practical content drawn from 25 years in the field.
What I take care of
- Good Clinical Practice and what changes with ICH E6(R3).
- Clinical research for principal investigators, CRAs and coordinators.
- Regulatory affairs: CTIS, ethics committees, ANSM, CNIL.
- Information sheets and informed consent, vulnerable populations, pharmacogenetics.
- Pharmacovigilance and device vigilance: reporting responsibilities.
- RECIST criteria and CTCAE toxicity grading.
- Source documents, investigational products and biological samples management.
- Protocol-specific training at study start-up.
Frequently asked questions
What sponsors, CROs and sites most often ask me before a mission starts.
On site or online?
Both: on your premises or as a virtual class, in French or English.
Need help with this?
Leave your details and a few words about your study: I will get back to you within 2 business days.