Taking your injectable drug product from development, through manufacture and then release to market involves a pathway filled with regulatory considerations and requirements.
With over 15 years of GMP sterile manufacturing experience, including GMP compliance to the highest standards currently recognised by the FDA and MRHA, discover how Symbiosis can help you navigate these regulatory complexities.
Download our regulatory capabilities sheet to discover more about the processes, quality systems and industry-leading expertise that we have built into every project to help get your life-saving therapy to patients as fast as possible.
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