16.01.2013 | Change in the Regulation Regarding the Packaging and Labeling of Medicinal Products for Human Use |
The amendments made with the “Regulation Amending the Regulation Regarding the Packaging and Labeling of Medicinal Products for Human Use” published in the Official Gazette dated 15.01.2013, with No. 28529, have been listed below.
REGULATION REGARDING the PACKAGING and LABELING of MEDICINAL PRODUTCS for HUMAN USE
Article 1 – Paragraph one in temporary article 2 of regulation regarding the Packaging and Labeling of Medicinal Products for Human Use published in the Official Gazette dated 12.08.2005, with No. 25904 has been changed as below.
"Serums, radiopharmaceuticals and private use products (excluding oral nutritional supplements and internal nutrition products) shall not be subject to datamatrix requirement until 01.01.2014"
Article 2 – Article 23 of the same regulation has been changed as below.
“Article 23 – The Director of the Turkish Medicines and Medical Devices Agency carry out the arbitrament of the articles of this regulation.”
Article 3 – This regulation is valid on 1/1/2013
Article 4 – The Director of the Turkish Medicines and Medical Devices Agency carry out the arbitrament of the articles of this regulation. |
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