Advice

Advice We are an organization specialized in the field of marketing & regulatory affairs of medical devices as well as in-vitro diagnostics.

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How to use

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Services


classification

  • American classification
  • European classification

regulatory services

  • Registration services
  • Importation Services
  • Customs clearance services
  • Exportation services
  • Local factory services

marketing services

  • marketing medical devices
  • marketing in-vitro diagnostics



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Work Process

Choose your product name & its class from the drop-list.
Choose the required service
Leave your whatsapp number & your email
Determine an appointment
Check your email

  • 01
    Classify

    Classify your product ( For Free)

  • 02
    Choose your product name

    Then Choose the required service

  • 03
    Leave a whatsapp number

    Leave a whatsapp number & a professional email Then determine an appointment

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Testimonials


Frequently asked question



Our team can help your company in the field of medical devices & In-vitro diagnostics in three aspects:
1- classification
2- Regulatory affairs
3- marketing

We offer this service for free. You can choose to get your product classified either by American or European classification or both.

1- Registration services
2- Importation approvals
3-Exportation approvals
4- Custom clearance
5- Local factory certificates

Simply, define your service & leave your whatsapp number & email & one of our team members will contact you.


About US

We are an organization specialized in the field of marketing & regulatory affairs of medical devices as well as in-vitro diagnostics. We help factories & companies getting their registration licenses , importation approvals & exportation approvals.

  • Vision

    To be the best source of information in the field of medical devices & In-vitro diagnostics.

  • Mission

    ⦾ Helping factories to legally circulate their products.
    ⦾ Assisting companies to gain their registration licenses & importation approvals.
    ⦾ Guiding health care practitioners to confirm the validity of medical devices & IVD.

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