Event price: No cost
Online payment: At the time of your registration you will be able to pay online with credit card and PSE.
Payment in banks:
Present the invoice printed in laser, and approach the following banking entities:
- Banco de Bogotá and its banking correspondents: Almacenes Éxito, Carulla, Surtimax, Súper inter.
Go to the University Cashier and pay with a debit or credit card.
Start date: 12-06-2020
End date: 12-06-2020
Duration: 0.65 hours.
Event city: Medellin
Hours: Thursday, June 12, 2020, from 06:00 pm to 06:40 pm
Place: Virtual classroom - CES University.
Event Code: 70082248
To register, you must fill out the form to generate the invoice and make the payment online, banks or in person at the University.
Learn about the importance of the topics to be addressed during the development of the Conference
We share the characteristics or requirements that you must meet to be part of this Conference
The modality of the event is Virtual
Medical Devices in Colombia are regulated by INVIMA, and within the framework of the current emergency, the flexibility of their requirements for national manufacture and importation has been granted. It is essential to know the traditional and current requirements to ensure the correct use of them in health care settings.
Professionals, university students, directors and heads of clinics and hospitals, Regulatory affairs managers, Technical Directors Coordinators / Directors of logistics of import companies and manufacturers of medical devices
Find out how you can finance your registration in this event.
Find the contents to be discussed in the Continuing Education Conference
Learn about the skills you will acquire by holding the Conference at our University.
Finance the payment of your registration with SUFI, contact the advisor:
Anderson Esneyder Acevedo Benitez
Telephone: (57) (4) 604 91 25
Mobile: 301 254 98 44
Payment with Severance:
Check with your fund and severance management company about the requirements to make the payment *.
* Applies for diplomas and certifications.
- Decree 4725 of 2005
- Resolution 4002 of 2007
- Resolution 522 of 2020 - Requirements
- Decree 476 of 2020
- Decree 538 of 2020
- Circular 031 of 2020
- Risk management
- International Standards
Publicize the requirements and standards associated with the regulation of COVID and NO COVID Medical Devices at the national level, in order to address best practices during the life cycle of medical devices with a risk approach.
Biomedical Engineer, Specialist in Project Management and Master in Administration. National expert in pre-market and post-market health regulation of Medical Devices.