Our advantages:
  • Professionalism and availability
  • Quality and performance
  • The rate of long-term cooperation
  • Full compliance with the norms and standards
  • Focus on results
  • Affordable prices
  • Privacy

Guaranteed result
  • Marketing authorizations, certificates of registration, certificates of conformity issued.
  • Declarations of conformity registered

The company "AiLFARMA"

has many years experience in the field confirm the quality and specializes in the registration of drugs, biologically active additives, raw materials for production of biologically active additives, medical devices, cosmetic products, personal hygiene items for children and adults, baby food, sports food, disinfectants in Russia and other countries.

And also develops the necessary documentation: specifications, technological instructions, instructions for use, reports, the summary on clinical tests, the normative document, etc

Ourcompetitive edge
High standard of the provided services owing to company’s skilled professionals boasting extensive work experience.
You can place an order for any service from any point of Russia.
We provide our services at the highest level

The complex of the services, rendered by the company,
includes a multilateral approach to the solution of objectives. We accompany you, since competent consultation on preparation of a necessary package of documents and finishing obtaining the registration certificate with the subsequent registration of certificates of conformity in GOST P system or declarations of compliance of production.
We well studied and perfectly we know a pharmaceutical market, highly skilled experts
therefore we possess actual information on development of the medical sphere work for us. We adhere to the high quality standards and principles of ethic business.
Customer feedback
"Гольфстрим" company
"Jeunesse" LCC company

Утверждены Правила формирования перечней лекарственных препаратов

Правительство РФ утвердило Правила формирования перечней лекарственных препаратов для медицинского применения и минимального ассортимента лекарственных препаратов, необходимых для оказания медицинской помощи

Приказ Минздрава России № 959н от 13.12.2016 г

Приказ Минздрава России № 959н от 13.12.2016 г. «Об утверждении классификации изменений, вносимых в документы, содержащиеся в регистрационном досье на зарегистрированный лекарственный препарат для медицинского применения» (Зарегистрирован в Минюсте России 09.01.2017 № 45123)

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