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European-Medical-Device-Regulation by Global Institute Regulatory Affairs

Do you want to Learn about EU MDR (European Medical Device Regulation)?

We Provide training courses on (EU-MDR/2017/745 & CE marking) with recorded lectures,

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This course will help you to understand:

The MDR’s additional requirements

The current directives – MDD 93/42/EE and ISO 13485:2016

Terminology and certification requirements

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WHO SHOULD ATTEND?

Manufacturers of medical devices, especially: Regulatory Affairs, Design and Development, Clinical Affairs Specialists, Quality Management, and Quality Assurance personnel.

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Hurry Up,

Register now at GIRA,

CALL/WHATSAPP For Enquiry:

+91-9595750750

More info visit:http://bit.ly/3sZQbEc

 
European Medical Device Regulation by Global Institute Regulatory Affairs

Do you want to Learn EU MDR (European Medical Device Regulation)?

We Provide training course on (EU-MDR/2017/745 & CE marking) with recorded lectures,

More info visit:http://bit.ly/3sZQbEc

 
European Medical Device Regulation by Global Institute Regulatory Affairs

Do you want to Learn about EU MDR (European Medical Device Regulation)?

We Provide training course on (EU-MDR/2017/745 & CE marking) with recorded lectures,

Hurry Up,

Register now at GIRA ,

CALL/WHATSAPP For Enquiry:

+91-9595750750

More info visit:http://bit.ly/3sZQbEc

#EUMDRtraining #regulatoryprofessional

#regulaatorycoursesinpune #regulatorytraining

#girapune #healthcare #europeanregulation

#medicaldeviceregulatorytraining

#medicaldevicecompliancetraining

#EUMDR #EUMDRprocess #EUMDRcourse

  
https://www.regulatoryinstitute.com/eCTD-training.html by Global Institute Regulatory Affairs

Training Program on European Medical Device Regulation,

Do you want to Learn EU MDR (European Medical Device Regulation)?

We Provide training course on (EU-MDR/2017/745 & CE marking) with recorded lectures,

.

.

WHAT IS EUMDR?

Implementation of European Medical Device Regulations is the primary requirement while demonstrating the compliance to regulatory requirements while placing the products in European Market for the Medical Device manufacturers and to place CE marking on the products.

.

.

WHO SHOULD ATTEND?

Manufacturers of medical devices, especially: Regulatory Affairs, Design and Development, Clinical Affairs Specialists, Quality Management, and Quality Assurance personnel.

.

.

Hurry Up,

Register now at GIRA ,

CALL/WHATSAPP For Enquiry:

+91-9595750750

More info visit:http://bit.ly/3sZQbEc

#EUMDRtraining #regulatoryprofessional

#regulaatorycoursesinpune #regulatorytraining

#girapune #healthcare #europeanregulation

#medicaldeviceregulatorytraining

#medicaldevicecompliancetraining

#EUMDR #EUMDRprocess #EUMDRcourse