Welcome to free breakfast seminar 31st May 8:30 - 9:30 am

Due to the high costs for product development, few small and medium-sized pharmaceutical companies will take their product to the market on their own.

Join us to listen to Niamh Kinsella, Principal Consultant, VP Early Stage Development, discuss the challenges facing early-stage companies on their road to meet critical business and development milestones.

Niamh will outline how planning can take both internal and external requirements into account to create a strategic roadmap for your development program. She will also discuss how early integration of regulatory requirements can be used as an important value driver for the product, enabling a global approach to maximise return on investment for the company as well as any partner.


  • Learn how to implement a stage-gate approach for the early development of your product
  • See how a global regulatory strategy can be implemented
  • Determine your strategy for agency interactions
  • Hear how NDA can help you

When: Wednesday 31st May 2017, 8:30-9:30 am. Breakfast from 8:00 am

Where: NDA Regulatory Service AB, Oxfordhuset, Johanneslundsvägen 2, Upplands Väsby

The breakfast seminar will be an open and interactive workshop with the opportunity to ask questions to Niamh and to the rest of the NDA team. Specific questions can also be sent in advance to frukostseminarium@ndareg.com
Indicate if you would like to discuss them openly during the meeting; otherwise, we can book separate meetings to discuss them after the seminar.

Registration: RSVP by Wednesday 17th May 2017 to: frukostseminarium@ndareg.com The number of participants is limited and we can only accept two participants per company.

Contact: Lina Jansson, Marketing Associate, +46 (0)8 590 778 00, or email frukostseminarium@ndareg.com

The breakfast seminar is free. If you are unable to attend, please advise us no later than two days before the seminar.




Niamh Kinsella

VP Early Stage Development


Stay up to date

Contact us

Your drug development needs are unique

Contact us to learn how our experts can support you to meet all regulatory, quality and safety requirements and ensure the best path to approval.

Let's Bring Medicines to the World

  • This field is for validation purposes and should be left unchanged.