MedStandard LLP of Almaty at MEDICA 2021 in Düsseldorf -- MEDICA - World Forum for Medicine
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MedStandard LLP

Karasay Batyr st 152/1 Office 500, 050026 Almaty
Kazakhstan
Telephone +7 727 2500011, +7 776 0055470
sales@medstandard.com

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Media files

Imagevideo MedStandard LPP

Hall map

MEDICA 2021 hall map (Hall 5): stand J05

Fairground map

MEDICA 2021 fairground map: Hall 5

Contact

Aidyn Jankurazova

President

Daniyar Issabayev

Chief operation officer

050026 Almaty, Kazakhstan

Phone
+7 (776) 250 05 65

Email
coo@medstandard.com

Evgeniya Gorodilova

115280 Moscow, Russian Federation

Phone
8 967 030 50 56

Email
ceo@medstandard.ru

Zhansaya Assanova

Chief business officer

050026 Almaty, Kazakhstan

Phone
+7 (776) 250 05 54

Email
cbo@medstandard.com

Ainelya Aitbayeva

Head of sales department

050026 Almaty, Kazakhstan

Phone
+7 (776) 005 54 70

Email
sales@medstandard.com

Aigerim Nazar

Head of the Accounting department

050026 Almaty, Kazakhstan

Phone
+7 (776) 250 05 68

Email
account@medstandard.kz

Damirlan Yessengaziyev

Specialist of Accounting department

050026 Almaty, Kazakhstan

Phone
+7 (776) 250 05 70

Email
account2@medstandard.kz

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Our range of products

Product categories

  • 07  Medical services and publications
  • 07.15  Technical equipment management, test houses / certification bodies

Technical equipment management, test houses / certification bodies

  • 07  Medical services and publications
  • 07.17  Other medical services and publications

Other medical services and publications

Our products

Product category: Consulting services for health organisations

Medical product registration stages, risk class 1, 2a (non-sterile products)

State registration of medical devices is a mandatory procedure, without which it is impossible to enter the market for products, their free sale, purchase and use.

During the procedure, the quality of the devices is checked and their compliance with the current norms and standards. Only truly high-quality and effective medical devices successfully pass all checks and are entered into the register.

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Product category: Consulting services for health organisations

Medical product registration stages, risk class 2a (sterile products), 2b, 3

State registration of medical devices is a mandatory procedure, without which it is impossible to enter the market for products, their free sale, purchase and use.

During the procedure, the quality of the devices is checked and their compliance with the current norms and standards. Only truly high-quality and effective medical devices successfully pass all checks and are entered into the register.

More Less

Product category: Consulting services for health organisations

In vitro medical product registration stages

The FDA classifies medical devices, including in vitro diagnostic devices, into Class I, II, or III according to the level of regulatory control necessary to reasonably ensure safety and efficacy. The IVD (or other medical device) classification determines the appropriate pre-sale process.

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About us

Company portrait

Regulatory Services Supporting Successful Outcomes End-to-End

Regulatory Affairs Support (also in EAEU Region)

- Medical devices
- Pharma regulatory affairs
- In Vitro diagnostic devices regulation
- Registration of Disinfectant Products
- Licensing of medical and pharmaceutical activities
- Medical equipment import licensing
- Registration of perfumery and cosmetic products
- Registration of dietary supplements

Metrology
- Approval of measuring instruments by type
- Metrological certification
- Verification

Company data

Number of employees 100-499
Foundation 2004
Area of business Medical services and publications