Virtual Classroom Training

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High-level introduction into centralized European procedure. This training is designed for Pharmacist, Physicians and other functions (Regulatory Affairs, Development) who want to better understand the centralized European procedure. But anyone interested in the topic can register.

Date: March 13th, 2025

Type: Virtual Classroom Training

Duration: 1 Day

Who should attend?: Pharmacist, Physicians and other functions (Regulatory Affairs, Development) who want to better understand the centralized European procedure

High-level introduction into centralized European procedure. The key learnings of this training are:

  • Understand the centralized registration procedure and the applicable texts
  • Understand the deadlines imposed and the expectations of the authorities at each stage
  • Anticipate the constitution of key elements

Anne-Valérie ANGERARD

Anne-Valérie has spent more than 20 years in regulatory affairs at the headquarters of pharmaceutical companies, with product portfolio management activities (MA, variation, advertising, medical devices, etc.). She has experience of decentralized and centralized mutual recognition procedures. From 2020 to 2022, in addition to her work in the pharmaceutical industry, she became a trainer at IMIS, where she put her experience in regulatory affairs at the service of students. In 2021, she joined Blue Reg, now Cencora PharmaLex, where she is in charge of regulatory affairs consulting for pharmaceutical companies of all sizes, covering a wide range of topics: regulatory positioning and strategy, registration, life cycle management, and answering questions from the authorities.

 

Anne-Valérie FAUCHER

Anne-Valérie has over 20 years’ experience in regulatory affairs, including 15 years at the head office of pharmaceutical companies, with activities in EU & Rest of World product portfolio management (registration and maintenance). In Europe, she has experience of decentralized and centralized mutual recognition procedures. In 2018, she joined Blue Reg, now Cencora PharmaLex, and is in charge of regulatory affairs consulting for laboratories of various sizes on a variety of subjects: regulatory positioning and strategy, registration, life cycle management, answering questions from the authorities.

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