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FULLY BOOKED: Synapse & Novo Nordisk presents: Regulatory Affairs – From R&D to Approval and Marketing

November 15, 2017 @ 5:00 pm - 7:30 pm

This event is now FULLY BOOKED:
Please write to nnra@synapse-connect.org with the topic “WL” if you want to be added to the waiting list. Write your name and phone number in the mail.

Join us on a company visit to Novo Nordisk in their Søborg offices as we explore Regulatory Affairs (RA) at Novo Nordisk, which is one of the most important processes of a major pharmaceutical company. Regulatory Affairs secures the approval of the next blockbuster drug and is involved in the entire drug development process, as well as all post-marketing life cycle management activities. To secure correct drug development, Regulatory Affairs interacts with all departments within the organisation from R&D to marketing and sales. A close collaboration with scientists to ensure new ideas will turn into successful products is thus a large part of Regulatory Affairs and is based on the ability to understand the science behind it.

During this company visit you will also be introduced to the Novo Nordisk Graduate Programme, which is a two-year program consisting of three 8-month rotations, each within a different department, and where one of these will take place in a global affiliate. The Programme is open to applicants from all over the world who have recently acquired a degree in the life sciences such as in pharmacy, chemical engineering, biology, biotechnology, biomedicine or a related field and is an exciting alternative career path for anyone who desires to use their life science skills outside of the lab. At the end of the programme, you will acquire an excellent set of skills within Regulatory Affairs which will prepare you for a successful career at Novo Nordisk, in Denmark or abroad.

Do you want to know more about the Novo Nordisk Graduate Programme and Regulatory Affairs? Join us on the 15th of November for an evening in Søborg where you will be taken through one of the most important departments in a pharmaceutical company. Besides gaining an insight into Regulatory Affairs, you will have the chance to meet young professionals from different areas across the Regulatory Affairs organisation including specialists, project managers and people managers, and both new and old graduates from the programme. Further information can be found HERE.

As an addition to the presentations, the participants will go through 3 rotations. In small groups of 10, each group will have 10 minutes together each with the 3 assigned professionals. Through this, Synapse aim to give you time and depth to go through your thoughts regarding both RA and affiliated departments

We are very proud to present the tentative list of professionals that you can meet during this event:
Nina Jordan, Senior Regulatory Intelligence Professional
Louise Wanning Tvede Anderson
, Labelling Coordination  Manager
Holti Kellezi
, Regulatory Professional Digital Health
Nicoline Victoria Anderson
, Regulatory Professional Oral GLP-1 & Early Diabetes Projects
Kahina Sehad
, Regulatory Professional CMC Modern & Human Insulins
Mark Joseph Root
, Senior Regulatory Professional Victoza®
Dominik Sawicki-Wrzask
, Labelling Professional
Elisabeth Thubron
, Regulatory Graduate
Volkan Kocak
, Regulatory Professional, Regulatory Information Managment System
Constanze Maria Hammerle
, Regulatory Professional, CMC GLP-1
Emilie Kaas Ibsen
, Business Analyst, Business Support
Dan Stenvall
, Labelling Professional

Programme:

Welcome:  17.00 – 17.15
Presentations:  17.15 – 18.00
Break: 18.00 – 18.20
1. rotation:  18.20 – 18.30
2. rotation:  18.35 – 18.45
3. rotation:  18.50 – 19.00
Dinner & networking:  19.00 – 19.30

Practicalities:

Date: 15th of November 2016
Time: 17.00-20.00
Place: Novo Nordisk in Søborg, Vandtårnsvej 108, 2860 Søborg
Meeting time: 16.45

A webform by Podio

 

Details

Date:
November 15, 2017
Time:
5:00 pm - 7:30 pm

Venue

Novo Nordisk Søborg
Vandtårnsvej 108
Søborg, 2860 Denmark
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