invites international partners for cooperation in contract manufacturing.
AVVA RUS JSC, a private Russian pharmaceutical company,
The manufacturing site of AVVA RUS
Established in 1996
Certificates of compliance with EU GMP, ISO 9001, ISO 13485
Sachets, suppositories and syrups: more than 200 million units
Annual production capacity: Tablets and capsules: more than 3 billion
Total area: 17 956 m2
Warehouse area: 2 420 m2
Number of employees: more than 500
Certificates of compliance with EU GMP, ISO 9001, ISO 13485
Sachets, suppositories and syrups: more than 200 million units
Annual production capacity: Tablets and capsules: more than 3 billion
Total area: 17 956 m2
Warehouse area: 2 420 m2
Number of employees: more than 500
The manufacturing site of AVVA RUS JSC includes:
- Facility for manufacturing of penicillin-like β-lactam antibiotics
· Capsules, powders, tablets, coated tablets
· Capsules, powders, tablets, coated tablets
- Facility for manufacturing of generic drugs
· Production areas for finished dosage forms, including tablets, coated tablets , dragées, granules, capsules, suppositories, syrups, and emulsions
· Production area for pellets, including pancreatine pellets
· Production area for finished dosage forms from hydrolyzed lignin, including the manufacturing of a substance and medicinal products based on hydrolyzed lignins
· Production areas for finished dosage forms, including tablets, coated tablets , dragées, granules, capsules, suppositories, syrups, and emulsions
· Production area for pellets, including pancreatine pellets
· Production area for finished dosage forms from hydrolyzed lignin, including the manufacturing of a substance and medicinal products based on hydrolyzed lignins
You can get more detailed information about our preparations here
https://www.avva-rus.ru/en/production/otc/
https://www.avva-rus.ru/en/production/otc/
In autumn 2017 the existing quality system and Good Manufacturing Practices at the AVVA RUS plant in Kirov were audited by European state auditors.
In January 2018 AVVA RUS obtained a EU GMP certificate eudragmdp.ema.europa.eu to manufacture medicines for human use, thereby confirming the highest quality standard of its products.
The products manufactured at the AVVA RUS production site can be registered and supplied in the Russian Federation, CIS, Mongolia, EU and other countries, which are current members of the Pharmaceutical Inspection Co-operation Scheme (PIC/S) (Portugal, Romania, Cyprus, Chile, Vietnam, etc.)
Currently AVVA RUS is dynamically involved in the implementation of Pharma 2020, a Russian state program.
In January 2018 AVVA RUS obtained a EU GMP certificate eudragmdp.ema.europa.eu to manufacture medicines for human use, thereby confirming the highest quality standard of its products.
The products manufactured at the AVVA RUS production site can be registered and supplied in the Russian Federation, CIS, Mongolia, EU and other countries, which are current members of the Pharmaceutical Inspection Co-operation Scheme (PIC/S) (Portugal, Romania, Cyprus, Chile, Vietnam, etc.)
Currently AVVA RUS is dynamically involved in the implementation of Pharma 2020, a Russian state program.
Gastroenterology
Pediatrics
Cardiology
Neurology
Allergology
Infectious diseases
The company specializes
in the following key areas
in the following key areas
AVVA RUS has been manufacturing products for more than 20 years, and its current portfolio includes about 50 efficient drugs, including both generics (Micrazim, Ecofuril, Ecofucin, Minoleksin, ecoantibiotics etc.) and original medicines developed by the company (Lactofiltrum and Filtrum).
In 2015, the Russian Ministry of Industry and Trade issued an order to include AVVA RUS JSC in the list of entities with a substantial impact on the industrial sector in Russia.
With its considerable experience in contract works and regulatory support, AVVA RUS is interested in localizing the products of international developers and manufacturers at its facilities and invites potential partners to mutually beneficial high-quality cooperation, including localizing the manufacturing of penicillin-like β-lactam antibiotics.
With its considerable experience in contract works and regulatory support, AVVA RUS is interested in localizing the products of international developers and manufacturers at its facilities and invites potential partners to mutually beneficial high-quality cooperation, including localizing the manufacturing of penicillin-like β-lactam antibiotics.
Advantages for potential AVVA RUS partners:
• Wide experience in Russian regulatory system
• Wide production capacities
• Status of drugs as medicinal products manufactured in the Russian Federation
• Public procurement sales opportunities with state support for Russian manufacturers
• Broad coverage of the national market, work with large distributors, presence in the pharmacy and inpatient sectors
• Advisory services of qualified health specialists
• Experience in the successful introduction of new brands to the Russian market and a highly professional marketing and sales staff
• Expert knowledge of all major therapeutic areas, including gastroenterology, otolaryngology, dermatology, pediatrics, gynecology and more
• Flexible approach to developing cooperation with partners
• Wide production capacities
• Status of drugs as medicinal products manufactured in the Russian Federation
• Public procurement sales opportunities with state support for Russian manufacturers
• Broad coverage of the national market, work with large distributors, presence in the pharmacy and inpatient sectors
• Advisory services of qualified health specialists
• Experience in the successful introduction of new brands to the Russian market and a highly professional marketing and sales staff
• Expert knowledge of all major therapeutic areas, including gastroenterology, otolaryngology, dermatology, pediatrics, gynecology and more
• Flexible approach to developing cooperation with partners
The production site is completely ready for track-and-trace which will be introduced in the Russian Federation in 2020. Among other things our R&D Laboratory can carry out a technical transfer and refine the composition and packaging to meet the requirements of the Ministry of Health of the Russian Federation.
To get a more detailed offer, please complete the feedback
form and our specialists will contact you as soon as possible.
form and our specialists will contact you as soon as possible.
