Regulatory Rapporteur October 2019
FOCUS: Falsified Medicines Directive PLUS • Latin America - Positive changes in the regulatory environment • CPD - European medical devices legislative framework • Virtual trials - Understanding the basics and exploring the benefits
Regulatory Rapporteur October 2019MEMBERS
Our experience of setting up the medicines verification systemMEMBERS
Safeguarding patients through serialisationMEMBERS
Understanding the basics of virtual and hybrid trials and their benefitsMEMBERS
Case study: a development strategy for a new combination product in the USMEMBERS
Positive changes in the Latin American regulatory environmentMEMBERS
Preventing fake medicines from reaching patients PUBLIC
Investigating potential inconsistencies in the summary of product characteristics PUBLIC
Developing a robust serialisation programme for the EU FMD PUBLIC