You will get 93/42/EEC (MDD) and 2017/745/EU (MDR) Consultant | Certification

Seyda K.Status: Offline
Seyda K.

Let a pro handle the details

Buy Other Admin & Customer Support services from Seyda, priced and ready to go.
Seyda K.Status: Offline
Seyda K.

Let a pro handle the details

Buy Other Admin & Customer Support services from Seyda, priced and ready to go.

Project details

With extensive experience in quality management for medical device companies and expertise in 93/42/EEC (MDD) and 2017/745/EU (MDR) regulations, I offer specialized consulting services to ensure full regulatory compliance. What sets me apart is my practical knowledge of both regulatory frameworks and hands-on support, tailored to the unique needs of your business. From detailed documentation reviews to full system audits and certification preparation, I provide a clear, actionable roadmap to help you navigate the complex compliance process efficiently and successfully.
Project Type
Customer Support, Other
What's included
Service Tiers Starter
$750
Standard
$1,350
Advanced
$2,500
Delivery Time 20 days 40 days 70 days
Number of Revisions
000
Seyda K.Status: Offline

About Seyda

Seyda K.Status: Offline
Translator & Medical Consultant
Izmir, Turkey - 7:31 am local time
I am a professional translator fluent in Russian, Uzbek, English, and Turkish, providing expert translation services.
With 3 years of experience in Quality Management and a certification as an ISO 13485 internal auditor, I specialize in ISO 13485 implementation and 2017/745/EU (MDR) / 93/42/EEC (MDD) compliance for medical devices. I offer consulting services to assist organizations in developing and improving their quality management systems, ensuring regulatory compliance and effective audits.

▪️Fluent in Russian, Uzbek, English, and Turkish.
▪️Offer translation services across various fields.
▪️2.5 years of experience in Quality Management.
▪️Specialize in ISO 13485, MDR, and MDD processes.
▪️Certified ISO 13485 internal auditor.
▪️Provide consulting for quality management systems in medical devices.
▪️Skilled in auditing, process improvement, and regulatory compliance.

Steps for completing your project

After purchasing the project, send requirements so Seyda can start the project.

Delivery time starts when Seyda receives requirements from you.

Seyda works on your project following the steps below.

Revisions may occur after the delivery date.

Starting work

Deciding on the work to be done regarding the process and delivering the files, if any.

Review the work, release payment, and leave feedback to Seyda.