You're a genius. Spend 5 minutes to Google what I wrote on other boards and on this board and you'll be in better position to cast doubts. Right now, you're just looking stupid and lazy. Google my friend! I don't support ashop neither Balkan or Vermodje. I've raised some doubts regarding the matters in discussion (Vermodje in this case) and I'm pretty impartial as you can see, I'm not throwing baseless claims left and right, I'm actually reading the documents posted up and interpreting them right as they are.

Why where the images removed? I can't see them anymore...

Lets be accurate. There is no HPLC testing on these 5 items, the reason why they are "Not corresponding" is because of "Marking reasons". That's what the certiticate is saying. We would like to see some real HPLC done on Vermodje products! Marking reasons can be various and people here don't care about that, I'm sure.

Translated .... used

www.bing.com/translator/ Date on report last summer

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AT THE PRESS-CAUTION

In the latest period, the territory of the European Union appeared more veterinary products of anabolic androgen steroids class, manufactured by VERMODJE SRL-Moldova.

In countries that have entered the market, these products are: Russia, Ukraine, Poland and Spain. 

Following quality tests in accredited laboratories have been established as major deficiencies: 

nonconformance with the composition of the content indicated on the packaging, subdozarea active principles, etc., relating to the manufacture in conditions that do not correspond to the European standards in force and the use of low-quality raw materials with chemical impurities content, solvents, salts of heavy metals. 

Management of the brand manufacturer concerned will not produce the desired therapeutic effect can worsen the condition and health of pet animals. 

Note that the content and quality of their serious injury may occur, on the health status of sportivilo

Second link doesn't say much.

Many of them are forced to cease the activity or to switch in manufacturers of veterinary doctors or fertilizer, because I can't get international certification.

Only four domestic pharmaceutical producers of those existing on the market 28 have already certified Good Manufacturing Practice (GMP), issued by the medicines agency, and 12 are in the process of implementation of these standards in manufacturing. At the same time, the other 12 producers are forced to close factories or transition, because they allow to synchronize production standards with the international force.

The Hope-Farm SRL, a manufacturer of pharmaceutical powders, which was closed. "The organisation has ceased trading recently because we can no longer sell any medications. Sell used equipment. I don't know what will happen next, "claims Lidia Trajan, representation of the company.

Vermodje LTD, a pharmaceutical enterprise in Ghidighici, who until last year was producing capsules and tablets, found a solution. "One year we have turned on the production of veterinary preparations. For these we have GMP certification, "said Victor clover, Director of the company.

Another company producing medications, however, serious problems in the implementation of GMP manufacturing standards. According to the nurses ' station at farmacistei-Com SRL, Mariana VitaPharm Stati, upgrading production lines, laboratories, implementation of technical parameters, storage space adaptation and completion of related documentation GMP certification costs about two million lei, which, she says, are not in the business.

"We can only sell their products on the domestic market, where our only added is limited by law to 15%. With an added can't do the GMP standards. We need a financial support from the State, to reimburse him. Otherwise, as a pharmacist, I am my work abroad. As a firm, we will probably make fertilizer, "says this.

Manufacturers, limit State

Certificate GMP eurofarmaco since 2006, being the first pharmaceutical manufacturer who has standardized the entire chain of production and distribution, according to the international standards in force. However, the company's Director, Boris Băluţel, claims that its competitors for that market, conditions for certification are much more difficult, because of the high costs of implementation, and the very short time that I have available.

"It's impossible to be connected at the GMP standards as pharmaceutical manufacturer in half a year, as the authorities require. GMP is not done in a day. Return to 15% limitation prevents the development of domestic producers. If something happens, you control all flow from the consumer to the supplier of the raw material. It's a huge job, "says Băluţel.

The Director of the drug agency, Alexander Cardona says, however, that all local drugs manufacturers who want to continue their business in this area should be to implement the GMP standards. "Producers need to understand that the pharmaceutical industry has some peculiarities and that it is necessary to hold this certification. The State provides them with methodological support. Those who fail can orient themselves to the manufacture of soft drinks or other activities. Each manufacturer has assumed the responsibility of introducing GMP standards over a period of time. Period may be extended, depending on each person's need, but not later than 31 December 2014, "said Cardoso.

Thorough standardization

To obtain the international certification of good manufacturing at the drug agency, pharmaceutical manufacturers must modernise their systems of acquisition of raw materials, chemical formula, creating conditions for transportation, storage and disposal, so any stage can be monitored in detail

Second one needs translated by members.