Approval, registration, certification of products for medical use – drugs, biotech products, medical devices, food additives, products for hygiene, veterinary and disinfection, medical equipment, cosmetics.

You made the decision to put your products to particular market. What you need? Do I need to get approval from the authorized agencies?

You do not have the time and resources for this – we can help you.

Our job is to require the approval of your product for its subsequent commercialization. You are interested in your products launch on the market of one country or group of countries in our region – we guarantee you entry to one gate to all your area.

 

 

 

 

You will receive:

  • 1Assessment of eligibility documentation in accordance with local laws
  • 2Identification of a regulatory strategy based on analysis of your product dossier
  • 3Support processes in the authorized bodies
  • 4Project Management
  • 5Interaction with stakeholders involved in the strategy of access products on the market- marketing, supply chain, commercial office
Registration of medicines is a long process, but thanks to us you will be able to register your products faster, having received a full package of permits.
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