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Medications play a major public health role by treating and preventing various diseases. Their production involves pharmaceutical manufacturing processes that drug manufacturers must adhere to. This is essential to ensure the effectiveness and safety of medications.
Medications play a major public health role by treating and preventing various diseases. Their production involves pharmaceutical manufacturing processes that drug manufacturers must adhere to. This is essential to ensure the effectiveness and safety of medications.
In this article, find out what you need to know about the pharmaceutical manufacturing process of drugs.
A medicine is defined by the Public Health Code (article L.5111-1) as “Any substance or composition presented as having curative or preventive properties with respect to human or animal diseases, as well as any substance or composition that can be used in humans or animals or that can be administered to them, with the aim of establishing a medical diagnosis or of restoring, correcting, or modifying their physiological functions by exerting a pharmacological, immunological, or metabolic action“.
Medicines play a threefold role by enabling the treatment of acute and chronic diseases, preventing the onset of certain illnesses, and improving the quality and life expectancy of patients by helping to manage disease symptoms.
There are two main types of medicines based on their pharmaceutical manufacturing principle :
The main steps in the pharmaceutical manufacturing of drugs are:
To learn more about primary pharmaceutical packaging, discover our complete guide.
Although the production of dietary supplements does not directly fall under pharmaceutical manufacturing, some dietary supplement manufacturers draw inspiration from pharmaceutical processes to ensure safety and efficacy.
To develop effective medications that address new diseases or emerging needs, pharmaceutical manufacturers must dedicate a portion of their efforts to research.
Thanks to preclinical studies evaluating the efficacy and safety of drug candidates, research enables the identification of new active molecules and the understanding of their mechanisms of action.
Clinical trials are studies conducted in humans with the aim of evaluating the safety and efficacy of medications.
This process occurs in several stages:
The Marketing Authorization (MA) is an official approval granted by regulatory authorities to any pharmaceutical manufacturer, allowing the commercialization of a medication. It ensures that the medication has been rigorously tested and meets safety and efficacy standards.
To find out more on MA, discover our complete MA guide.
Pharmaceutical manufacturing of medicines and dietary supplements is a complex and rigorous process, essential in guaranteeing the safety and efficacy of our products.
Thus, to offer its partners, manufacturers of dietary supplements and pharmaceuticals, high-quality double-pointed glass ampoules, SFAM favors manufacturing processes in line with pharmaceutical drug manufacturing standards, such as:
To learn everything about ISO standards in pharmaceuticals, discover our guide.