Training | 2020.06.30
FDAnews Announces — EU-MDR Postmarket Surveillance: Best Practices for Medical Device Regulatory, Compliance & Quality Specialists Webinar, July 14, 2020
Confused by new EU-MDR postmarket surveillance requirements? Easily handle reporting with this training on best practices.
(PRWeb June 30, 2020)
Read the full story at https://www.prweb.com/releases/fdanews_announces_eu_mdr_postmarket_surveillance_best_practices_for_medical_device_regulatory_compliance_quality_specialists_webinar_july_14_2020/prweb17229598.htm
For more information, please visit
https://www.prweb.com/releases/fdanews_a[...]july_14_2020/prweb17229598.htm
