Pharmaceutical engineering, technology and production
In 1992, a team of highly qualified technologists and pharmacists from Czech pharmaceutical industry established FAVEA s.r.o.
The main object of the company is to provide engineering services in the field of pharmaceutical facilities, both for new-built and renovation projects implementing the latest technologies. In 1998, FAVEA built a modern pharmaceutical object, which includes:
Production of solid dosage forms; Production of ointments and creams; Center for Research & Development of new medicines; Training Center for different pharmaceutical technologies.
In 2000, to improve effectiveness in the realization of pharmaceutical production and organization of complex technological equipment supply FAVEA set up a subsidiary company FAVEA Europe, s.r.o., as well as its office in Russian Federation “FAVEA Engineering Rus“.
Currently our company has following parts and activities:
FAVEA, s.r.o.
Research & Development of new drugs;
Production of pharmaceutical and cosmetic items;
Training qualified personnel for the production in compliance with standard of GMP.
FAVEA Europe, s.r.o.
Development of pharmaceutical production projects;
Projection works in compliance with international standards, Russian norm GOST R 52249-2004 introduced in 01.01.2005, and Ukrainian norm - DBN A.2.2-97;
Pharmaceutical and medical engineering;
Organization of construction works;
Complex supply of clean rooms in compliance with requirements of GMP standards and ISO 14644 (space planning, doors, floors, ceilings, lighting, filters, ventilation grates, etc.);
“Turnkey” installation of clean rooms, including ventilation and air condition systems etc.;
Delivery of special stainless furniture for clean rooms;
Delivery of the pharmaceutical technological equipment;
Delivery of equipment for gaining, distribution and storage of water PW and water for injection WFI;
CIP / SIP stations;
Installation and launch of the technological and auxiliary equipment;
Startup of pharmaceutical production;
A full validation of the pharmaceutical production in compliance with the GMP: the specification of the project, specification of clean rooms and ventilation systems, specification of technological equipment and engineering systems, validation of processes including the validation of projection documentation;
Training of qualified personnel for our Customer.
This year “Platinum Ounce” award in the special category of the organizing committee for the “Successful implementation of projects on modernization of pharmaceutical production in Russian Federation in accordance with the standards GMP” received company FAVEA
The worldwide most important document in determining the requirements for production and quality control of medicines for humans and animals is "Good Manufacturing Practice for Medicinal Products (GMP)".
Validation
In the methodological guidance we take into account the most recent issues of the national normative documents, the recommendations of the World Health Organization (WHO) and the Convention on mutual recognition of inspections in ...
GMP Training
The purpose of this training is to deepen the fundamental knowledge and expertise on the development of modern pharmaceuticals, manufacturing and quality control. Important objective is to train the personnel, ...
