Medical Devices Course
1-2 November 2018
Riga, Latvia

 

LEARNING OBJECTIVES

  • GAIN a complete overview of the latest MD regulations
  • MEET the requirements for MD labelling and CE marking
  • COMPLY with MD vigilance requirements
  • KNOW requirements for MD distribution
  • EXAMINE the role of Competent Authorities and Notified Bodies
  • UNDERSTAND adverse event reporting for MD
  • MAKE successful reimbursement and compensation applications
  • WORK effectively in MD sales

WHO SHOULD ATTEND

  • Regulatory Affairs professionals seeking to improve their skills in regulatory environment
  • Those moving into Regulatory Affairs from otherareas within a Medical Device company (Clinical Trials, Marketing and others)
  • Anyone wishing to update their knowledge on EU Regulatory Affairs

I would like to participate for:

  Date Course Full price VAT Total Price

Information about participant:

First Name*
Last Name*
Job Title*
Mobile No.*
Email*
Any special requirements
Company Name*
Company Address
Tel. number
Billing address (if different)
Reg. number
VAT number

Interest Form

Tick the topics that might be of your interest
CANCELLATIONS: Confirm your cancellations in writing 3 weeks before the date and receive a 50% refund. Should you cancel between this date and 1 week before the date of the course regrettably you will not receive a refund. Customer may reschedule a booking to another date at a 100% rescheduling fee by advising Rephine Balticum of such rescheduling in writing. It may be necessary for reasons beyond the control and the organiser to alter the content and timing of the program or the identity of the trainers. In the unfortunate event that an event is cancelled Rephine Balticum are not liable for any costs incurred by delegates in connection with their attendance. This contract is subject to Latvian Law.