Regulatory workshop: PREPARATION OF DOCUMENTED PROCEDURES FOR MEETING THE REQUIREMENTS OF THE NEW REGULATION IN THE FIELD OF DISTRIBUTION OF MEDICAL DEVICES

Eighth term: 14h November 2019 (FULL)
raPHARM premises, Miklošičeva 30, Ljubljana (Slovenian language)

Nineth term: 28h November 2019
raPHARM premises, Miklošičeva 30, Ljubljana (Slovenian language)

Tenth term: 23rd January 2020
raPHARM premises, Miklošičeva 30, Ljubljana (Slovenian language)

Regulatory workshop
PREPARATION OF DOCUMENTED PROCEDURES FOR MEETING THE REQUIREMENTS OF THE NEW REGULATION IN THE FIELD OF DISTRIBUTION OF MEDICAL DEVICES

The workshop is intended for all economic operators (distributors, sellers, importers, authorized representatives and manufacturers) of medical devices included in the supply chain of medical devices that need practical knowledge of distributors’ obligations as described in the new regulation, together with additional guidelines and approaches, which can be used to fulfill these obligations.

The acquired practical knowledge and appropriate proposals for the gap analysis, process inventory (OP/SOP) and the keeping of records that you receive will help you identify, adapt and/or establish appropriate procedures in accordance with the new legislation, suitable for your business mode and medical devices class.

Click HERE for more information on the workshop.

Click HERE to apply for the workshop.