Development of Documents for Collection of Dossiers for Registration of Medical Devices
If, after the Initial Diagnostic, we realize that your Dossier is not ready for the Registration process of your medical device - we can assist in developing the missing documents, as well as correcting the existing ones.
development of QMS documents in accordance with ISO 13485
laboratory testing of medical devices
lot release assessment
amendment and re-registration of the Registration Certificate
It's easy to get started with us
Apply by any
conveniently way
We're doing Preliminary
Diagnosis of your documents
- in 3 hours for FREE
Start the registration process
of the medical device, either start
document development, if needed
5 guarantees from LIMI Consulting Service
1
We set realistic prices and adequate deadlines. Always.
2
We always take into account post-registration risks when preparing Dossiers
3
We guarantee absolute transparency of the processes and quality of the developed documents
since we know how government authorities work from the inside
4
We work quickly and comprehensively - no outsourcing, only in-house experts
5
Never promise what we can't deliver.
TEAM
Diana Arys
Founder, expert in document development
"If she takes on something, she does it well and to the point. Always."
Olzhas Akhmetsadyk
Founder, expert in medical device registration
"I am convinced that success comes through Partnership and Expertise"
Diana Thanatar
Senior project manager
"I am convinced that the value of work is born in the balance of professionalism and human approach"
Айгерим Мамыраим
project manager
«Считает, что внимательный подход и понимание процесса помогают находить правильные решения»
Almira Hamza
Project manager
"The main principle in the work is thorough analysis and full understanding of the process."
Назымгуль Елемесова
project manager
«Мой принцип в работе — постоянное развитие, ответственность и командная работа.»