Following the publication of the latest European regulatory texts clarifying notified bodies’ practices on timelines, costs, and re-certification, the MDR and IVDR are directly impacting manufacturers’ global market access strategies. From the perspective of a Notified Body, see how these changes are reshaping decisions to enter the EU market and how market strategy and experience gained through MDSAP as a regulatory pathway in different countries can be leveraged as a strategic global market access pathway to mitigate complexity and accelerate international expansion. Join the RAPS DC/Baltimore Chapter for a roundtable discussion and network with peers in the region.
Location
Juniper Room
2600 Tower Oaks Blvd
Rockville, MD 20852
Proof of Attendance
A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.
Cancellations and Refunds
RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation. All cancellation requests must be submitted in writing to [email protected]. Cancellations will receive a full refund minus a 20% administrative fee. RAPS is unable to accept cancellations by phone.
Substitutions
Paid registration substitutions may be accepted with written approval from RAPS for requests received before the start of the event. To transfer a registration, email [email protected] with the event title, name of the original registrant and the contact information for the new attendee.
Questions
Contact the RAPS Support Center:
Call +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email [email protected].
Speakers
