Related articlesThe agency is responsible for the scientific evaluation of medicines developed low levels of potassium pharmaceutical companies for use in the EU. All medicines for human and animal use derived from biotechnology and other high-tech processes including biosimilars must be approved via the centralized Somatropin ema guidelines procedure. Guideline on similar biological medicinal products containing biotechnology-derived proteins as active substance: Guideline on similar biological medicinal products containing biotechnology-derived proteins as active substances: Specific Guidelines These guidelines are specific soomatropin the type of biosimilar product:. Draft Specific Guidelines EMA has the following draft somatropin ema guidelines under public consultation to develop guidelines for specific biosimilar products:.
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