This company has been trading in pharmaceutical substances, producing and marketing prescription drugs and over-the-counter medicines, nutritional supplements, generic drugs, cosmetics and medical products for more than 10 years.

Naturally, Euro OTC Pharma GmbH was granted a manufacturing permit according to the German Pharmaceutical Law (Art. 13 AMG) as well as a wholesale license according to Art. 1 AMG The pharmaceutical industry in the European community is committed to maintaining the highest standards of quality control during development, manufacturing and monitoring of drugs. 

The Good Manufacturing Practice (GMP) guidelines are implemented to ensure that these tasks are carried out only by qualified manufacturers who have been granted the required permits, and who are continuously being monitored. This represents the prerequisites necessary for the production of drugs.

EURO OTC Pharma provides drugs that have undergone reprocessing, assimilation, conversion, decanting and rebottling, prepackaging, labeling or after being approved. All products are subjected to stringent quality assurance tests before release. Quality assurance includes monitoring the properties of each product in regards to safety, quality standards and efficacy.

Such high standards are applied during the evaluation of suppliers and extend to manufacturing and quality control, ensuring seamless implementation through regular inspection Operating the new production facility allows Euro OTC Pharma GmbH to expand and optimize its capacity according to its slogan “Service through Competence and Strength”. This slogan is applied in all stages and is supported by expertise, commitment and dedication This company strives to make the impossible possible, responding to all your requirements and wishes through maximum flexibility.

www.euro-otc-pharma.de