Patient safety and health are a top priority for us, so we ask healthcare professionals and patients to notify us of any side effects, adverse reaction and/or inefficiency during use of our products.
This information allows permanently monitor benefit/risk balance of a medicine, to implement and maintain at the appropriate level the necessary minimization risk measures.
If you wish to report an adverse event, adverse reaction and/or ineffectiveness occurred during use of our products, please fill out the form below.
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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.
