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NEW HEMOFARM PREPARATIONS TO APPEAR SOON

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active component, the great proportion of the active component in the tablet mass. Following successful selection of the<br />

most optimum formulation and production technique based on laboratory research, and followed by stability results,<br />

research was conducted also of the bioequivalence of the dose of 100 mg. In vitro and in vivo tests proved that our<br />

product was bioequivalent with the originator, under the patented name Cozaar, more precisely with the product<br />

registered on the German market under the name Lorzaar film tablets of the producer Merck Sharp & Dohme.<br />

The following diagram shows the results of the in vitro tests of the release of the active component for our and the original<br />

product:<br />

The efficiency, safety and quality of our generic product<br />

has been confirmed through all development phases by<br />

excellent results in the physical-chemical and biologicalmedical<br />

researches. The trend of such good results<br />

continued in the first transfer phase in the production, so<br />

that we expect positive opinions and release of the first<br />

batch by the Agency for Medicaments.<br />

Hemofarm Institute<br />

Staša Vuković<br />

New Product Development Project Manager<br />

R&D Department<br />

STADA R&D MEETING IN VRŠAC<br />

35 representatives of all business units of the STADA group stayed in Vršac from September 17 to 19 in the aim of<br />

attending the regular half-yearly R&D meeting, which was held in hotel Villa Breg and was hosted by our company.<br />

Considering the significance of the meeting at which the production portfolio was defined for the whole STADA group, our<br />

president Mr. Miodrag Babić, vice-president Mr. Nikola Stanković and the executive vice-president Miss Sonja Pejović<br />

took also part. Mr. Babić made a statement to the attendants at the very beginning of the meeting, wishing them welcome<br />

and successful work and then he made a brief presentation about Hemofarm. Our president pointed out that Hemofarm<br />

was a company in which medicaments were developed and produced to be distributed throughout Europe and he invited<br />

the participants to visit our plants on the second day so as to get assured about the good equipment in all of our plants and<br />

laboratories, but also about the expertise and competence of our staff.<br />

Mr. Christof Schumann, member of the STADA group board and the R&D directors Miss Sigrid Dienel and Mr. Michael<br />

Wolf-Pflugmann presided over the working part of the meeting. Consideration was given to the status of the earlier defined<br />

development projects and new projects were proposed during the whole day of work. It was maintained once again that<br />

under the conditions of the ever increasing market competition there is a great pressure on the R&D, which must provide<br />

new products using the available resources, but also strategic approaches. It was pointed out that STADA got<br />

development facilities with the acquisition of Hemofarm, which will enable more and more new products to be developed<br />

in its own laboratories, whereby better control over projects is achieved, and later better management of the production<br />

costs. New projects which would be developed in the Hemofarm institute were defined in this sense, with the intention to<br />

register and place them on all markets on which STADA operates.<br />

A visit to the Hemofarm production facilities was organized on the second day, whereby all guests expressed sincere<br />

satisfaction with what they saw. They also praised the excellent organization for which the Hemofarm Institute and the<br />

president’s cabinet were in charge of and expressed a wish to to gather again in our town.<br />

Vjera Pejanović<br />

Hemofarm Institute Director

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