We are a team of professionals who guarantee priority responsibility in the implementation of the assigned tasks.
We have 10 years of successful experience in the field of regulatory activity in the Republic of Uzbekistan and CIS countries.
Our service is one of the leading and created for optimal collaboration with empowered and authorized government organizations.
High responsibility to the process, creative approach and diligent work to ensure quality are crucial for us.
50
Entrusted partners
15000
Completed works
350
Finished projects
Short list of supplied works and services:
Preliminary research
Consultation, assistance and support, search and analysis of information on trademarks (objects of intellectual property), substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Development and localization of documents and materials
Collection, preparation and verification of data for registration documents (dossier) of substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Product approval and authorization
Organization of the process and state registration of trademarks (patent protection of intellectual property objects), substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Verification and preparation of documents and materials
Organization of the process and re-registration (renewal) of the registration certificate (RC, marketing authorization) of trademarks (patent protection of intellectual property objects), substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Implementation of changes and amendments
Organization of the process and variation (amendment) to the registration documents of trademarks (objects of intellectual property), substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Research and investigation
Organization of the process and conduct of preclinical, clinical and postclinical studies of finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Good Pharmacovigilance Practice
Organization of the process and conduct of pharmacovigilance, monitoring of side effects of finished medicinal (pharmaceutical) products (FP medicines), nutraceutical producs (dietary supplements) and etc.
Declaration and customs clearance
Organization of the process and certification of substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Management, troubleshooting, support and acceleration of the processes
Control of work, search of solutions to the received issues (requests) for substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Verification and preparation of documents and materials
Design, edition, preparation, preprint adjustment, of packaging artworks (layouts), promotional materials, printing products for substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Approval of maximum sale prices
Organization of the process and registration of reference cost for substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Generation of marking codes ASL BELGISI
Organization of the process and registration of digital marking codes (Data matrix, Means of identification of the motion monitoring system) for substances (API), in-bulk products, finished medicinal (pharmaceutical) products (FP medicines), medical items (devices) and medical equipments, nutraceutical producs (dietary supplements), cosmetics and etc.
Still in doubt? Review our distinctive potential and special features
Medical product can be produced, sold and used only in case if properly registered and (or) confirmed in accordance with current legislation.
Want to know about the process? Find out the clear and brief description
Description of the main stages and work condition
Analysis, consultation and determination of the order of work.
Verification of the received data.
Processing and development of documents.
Checking, verification and reconciliation.
Transfer of documents to the empowered and authorized authority.
Management and support of the process.
Rapid help to speed up the process.
Completion of the process.
Transfer of finished documents.
Still have any questions? Please feel free for contact