Basic requirements to sell Medical & IV Diagnostic devices in Canada

In this webinar recording you will hear the requirements and fees for all type of medical device classifications.

Kanada'da cihaz kaydı yapmayı planlayan tibbi ve tanı cihazı üreticilerine temel konuları anlatıyoruz.

Consultant: Ray Kelly - Arazy Group

Recording Date : 4 October 2023 

 

Eğitmenler

Chief Regulatory Officer at Arazy Group Consultants Inc. Arazy Group introduced LICENSALE® in 2013, an advanced registration and license management technology solution designed specifically for regulatory affairs professionals in the medical and IVD device industry. Since then, it has been widely used in new product registrations, license amendments, renewals, and transfers. Leveraging on experience, software database management, machine learning, and A.I., Arazy Group launched the next medtech registration technology platform LICENSALE 2.0, which includes LICENSALE®- Global Medtech Registration System and REGISLATE® - Global Medtech Registration Management Software (RMS). These products currently serve over 2,200 medical device manufacturers and cover services in 140 countries.

Diğer Seminerlerimiz
2017/745 MDR Semineri
Devamını Oku
EN ISO 13485:2016 Kalite Yönetim Sistemi Semineri
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ISO 31000: 2018 Risk Yönetim Kılavuzu Semineri
Devamını Oku
Elektrikli Tıbbi Cihazlar için Testler Semineri
Devamını Oku
EUROFINS Semineri - Tıbbi Cihazların Biyolojik Değerlendirmesi
Devamını Oku
Süreç Validasyonu Semineri
Devamını Oku