When registering biologically active additives, the commission devotes an important role to packaging and packaging
materials.
What are the requirements for the packaging of biologically active additives? What will the attention will be paid to
E specialists during registration and consumers when buying?
There are several mandatory requirements. Failure to do so means a failed registration attempt.. На упа
forging should be indicated in Russian, that a biologically active additive is not a medicinal
remedy, All components are listed in descending order. Если в составе биологически активной добавки е
Food substances, It is necessary to indicate their content in absolute expressions and as a percentage of the river
ендуемой суточной нормы потребления. Directions for use, dosage, Indications for use and antip
Provision for use of additives. Basic requirements for component composition, The possibility of application
various groups of the population, The need to apply special inscriptions are spelled out in TR TS
021/2011 and tr ts 022/2011.
This is all?
No. Besides, date of manufacture must be indicated, storage conditions and expiration dates. Обратите вним
infusion, that there should be information about state registration indicating the details of Dokume
нта и его даты выдачи. And manufacturer's contact information. Обязательно указывать контактные данные
компании, которая отвечает за претензии потребителей.
What are the most common mistakes when preparing packaging??
Очень частой ошибкой становится помещение на упаковку фразы «экологически чистый продукт». Это ошибка
– для характеристики пищевых продуктов такой термин не применяется. Еще одно важное замечание, translation
е нередко производителями игнорируется – не допускается вынесение на этикетку биологически активной доб
авки информации о том, that the product is of natural origin, потому что этот факт не гарантирует н
и высокого качества, No security for humans.
If the additive has passed the check and was registered, Means, it is recommended for sale?
Такие сведения запрещено публиковать на упаковке. Несмотря на положительное решение относительно реги
Strazia, It is prohibited to indicate the recommendations of the Ministry of Health.
But some excerpts from official documents should be?
Yes, The text of the label on the package in the part of the “Indications for use” should fully correspond to the content
the same item in the registration document. The main recommendations for the development of the layout you
Find in TR TS 022/2011.
Thus, packaging must contain only those data, which you listed and, we see, a certain in
Formation on the beneficial properties of additives?
In no case: placing on the label information about the special beneficial properties of the additive, As well as about p
олном отсутствии у нее побочных эффектов не допускается. Были случаи, when the package was indicated
the possibility of replacing a specific therapy with an additive in case of human illness or other information, To
otor can mislead the consumer regarding the properties and effectiveness of biologically asset
Noah additives.

Instructions for use should not contain explicit medical recommendations., Diet can only
contribute, improve, be recommended, source of missing components.
As for the packaging material? There are some features here?
Certainly, Hygienic requirements should meet not only the label, but also the quality of packaging
materials, которые непосредственно контактируют с биологически активной добавкой к пище. Главное усл
ivi - they must be in the prescribed manner permitted to use.
Is it necessary to take care of the packaging in advance or is this not the first stage of registration of the additive?
About packaging, undoubtedly, стоит подумать сразу. Хотя при постановке на производство экспертиза упаковки не
самый первый этап. Если говорить обо всех ступенях контроля, то необходимо будет пройти следующие: эксп
ертиза технической документации – технические условия, технологическая инструкция, Explanatory note
and on the scientific substantiation of the composition of the additive; Examination of the production control program is produced
product at the enterprise-
изготовителе с выделением критических контрольных точек. Затем тот самый этап, о котором мы говорили – э
consumer packaging for compliance with the established requirements for contact with food
продуктами или лекарственными средствами. И только потом исследование образцов сырья или готовых биол
Ogically active additives for safety indicators.
When registering foreign dietary supplements, the following features can be identified: contract production,
Lack of distributor in the market. All this complicates the process of state registration and requires
providing additional documents. You can contact our company for clarifications.
На первый взгляд контроль над подготовкой упаковки несложный этап. Какую помощь здесь могут оказать сп
Etialists of the Consulting Center?
In-
the first, This help in preparing a packaging project - this will help to avoid mistakes and significantly reduce
т издержки. In-
second, If the manufacturer has refused consultants, то в 90 процентах случаев ему придется корре
the project - in this case, our experts will come to the rescue.