FAVEA projects
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Training Course for Kazan’s pharma-technologists in Czech Republic
This January OAO “Tatchimpharmpreparaty" (Kazan) arranged a training course for its group of technologists, held in Koprivnice (Czech Republic).   The group of specialists from Medical Products Development department was led by Deputy of General Director Mr. I.R. Abdullin who manages development of new technologies and medical products, and chief technologist of OAO “Tatchimpharmpreparaty" – Mrs. N.V. Matrina.

The principle mission of this visit was a research work concerning development of the new products – so called “generics” which are expected to extend a product portfolio of OAO “Tatchimpharmpreparaty" in the near future. The production facilities are based in the new workshop constructed and equipped in 2008 by FAVEA company in strict accordance with GMP standards.

FAVEA - Training Course for Kazan's pharma-technologists in Czech Republic

Practicing of manufacturing processes as well as theory program of training have been organized on the basis of production facilities of FAVEA in Koprivnice, with participation of Managing Director, Research Manager – Pharm.D. Milan Krajček. During the training course the trainees have attended some lectures dedicated to actual issues of development, manufacturing and analysis of solid dosage forms. Particularly, the reports about methodology of tablets’ composition development, peculiarities of granulation, pelletizing and coating have been lectured by Dr. Krajček who is known as European key specialist in pharmaceutical technologies. Besides, the trainees have attended some lectures dedicated to important aspects of the good manufacturing practice in pharmacy.

FAVEA - Training Course for Kazan's pharma-technologists in Czech Republic

/>Particularly, the Quality assurance manager of FAVEA, Mrs. Karin Stankova, has made an interesting presentations dedicated to establishment and application of the production quality control system, and special GMP requirements relating to pharmaceutical documentation. Specialist of new products certification, Mrs. Alexandra Piskorova, has shared an experience concering the clinical trials of new medicines, and specifics of their certification in European Union. The lectures of Lucie Flajsarova, the validation specialist of FAVEA, have attracted a particular interest of the trainees. Having a considerable experience in validation of various pharmaceutical processes, Mrs. Flajsarova gave a detailed answers to all the questions of participants.

Besides, in the course of training, the attention was paid to clean room facilities issues such as equipping, working air parameters and quality of purified water. These issues were repoted by principle engineers of FAVEA – Mr. Jiri Needly and Mr. Frantisek Krenek.

After two weeks of collaboration, Dr. Milan Krajcek acknowledged a high qualification of Kazan’s technologists, and expressed his hopes of further cooperation with OAO “Tatchimpharmpreparaty" At their leisure time the guests from Kazan have had a wide range of cultural activities including sightseeing tours around the historical parts of Prague, Karlovy Vary and Moravia.

FAVEA - Training Course for Kazan's pharma-technologists in Czech Republic

It is worth to underline that FAVEA helps its customers not only to upgrade their facilities according to GMP requirements but also renders assistance in creation and development of medical products technologies as well as in education of high qualified pharmaceutical personnel of various scopes. The illustration of such support is a long-term successful cooperation between FAVEA and OAO “Tatchimpharmpreparaty".

Press-centre of FAVEA
 



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

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Opening of a new pharmaceutical production in Kazan

Opening of a new pharmaceutical production in Kazan

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The new production of growth hormone RASTAN in Ufa

GMP Standard

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, ...

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