A full range of services for the registration and certification of medical devices and pharmaceutical products, as well as related regulatory support services for manufacturers and distributors of medical products

MEDITOR – Expert Regulatory Consulting for the Healthcare Industry

To help ambitious companies grow and scale their businesses faster while maintaining a strong focus on quality and information security.

Our Mission

Our goal is not only to help companies successfully complete certification and registration procedures but also to ensure their long-term market success by reducing risks and improving operational efficiency.

We provide a complete range of services - from regulatory consulting and compliance guidance to support during product development and commercialization - allowing our clients to focus on innovation and business growth.

We consider not only technical and legal aspects but also the impact of human factors on the safety and effectiveness of medical devices, offering solutions designed to improve interaction with end users.

We help our clients navigate complex regulatory requirements across different markets, ensuring full compliance and accelerating market entry.

To contribute to the development of a transparent and efficient regulatory environment in which medical products comply with the highest safety and quality standards and become accessible in international markets.

Our Vision

Our Priorities

Everything Is

Easier With Us

01 —
Free Consultation

We answer your questions, recommend the most suitable solution, and prepare a detailed commercial proposal

06 —
Issuance of the Registration Certificate

We obtain the registration number and secure the issuance of the Medical Device Registration Certificate

02 —
Product Audit

We immerse ourselves in your business, assess your product’s strengths, analyze competitors, and recommend the most effective market positioning strategy

04 —
Expert Review

We assess documentation for safety, effectiveness, and quality. When required, we arrange sample testing and verify analytical methods

05 —
Safety Assessment Report

We issue a document containing a consolidated assessment of the safety, effectiveness, and quality of medical devices

03 —
Dossier Preparation

We collect product documentation, obtain product samples, and enter into an agreement with the authorized state certification body

Our Process

Free Consultation – Your First Step Toward Success!

We will show you how to overcome your challenges and develop a customized strategy tailored to your needs.

Your Reliable Partner for Medical Device Registration!

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66 Navoi Street,
Almaty, Kazakhstan