The information put on packing materials shall conform to the current laws. It is very important in view of provision of continuous circulation of a product on the target market and for avoidance of utilisation of series of products due to their non-conformity to the approved registration materials.
development of the text of marking
approval of a text of marking in the competent authority (if it is required by the current laws)
graphic layout setting
regulatory analysis of packing
approval of packing for printing
introduction of package designs to the unified database of the State Service of Ukraine for Medicinal Products (for medicinal products in Ukraine)
development of the text of marking
approval of a text of marking in the competent authority (if it is required by the current laws)
graphic layout setting
regulatory analysis of packing
approval of packing for printing
introduction of package designs to the unified database of the State Service of Ukraine for Medicinal Products (for medicinal products in Ukraine)
MAXIMA Health Research with long-term experience in registration and post-registration support of different kinds and types of products has profound knowledge of requirements of the current laws and offers you to carry out any required regulatory procedures qualitatively and quickly, and most importantly according to the current laws and strategy of the company.
Our company successfully provides services for regulatory activity to pharmaceutical and FMCG companies, so we are ready to answer any of your questions.
