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GMP certification is a process that is carried out in order to determine whether the manufacturing processes of a company meet the requirements of the GMP guidelines. The GMP guidelines are set forth by the World Health Organization (WHO) and are designed to ensure that products manufactured by pharmaceutical companies are safe, effective, and of good quality.
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CE Certification is a mandatory conformity mark for products placed on the market in the European Economic Area (EEA). The CE mark indicates that a product has been assessed by the manufacturer and found to meet all the appropriate provisions of the relevant European health, safety, and environmental protection legislation.
https://www.iascertification.c....om/ce-marking-certif

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