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What Role Does Regulatory Affairs Play? | Pharmaceutical Science

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They are responsible for preparing and submitting <a href="">regulatory documents</a> to agencies like the FDA or EMA, and for ensuring that any clinical trials or manufacturing processes meet stringent regulatory standards. Their work is crucial for obtaining approval to market new drugs.</div></div> </div> <hr /> <h3 class="rq-heading">Frequently asked queries:</h3> <div class="qa-container"> <div class="qa-item"> <a href="https://thepharma.net/knowledgebase/what-is-pharmaceutical-science" title="What is Pharmaceutical Science?">What is Pharmaceutical Science?</a> </div> <div class="qa-item"> <a href="https://thepharma.net/knowledgebase/how-are-new-drugs-discovered" title="How are New Drugs Discovered?">How are New Drugs Discovered?</a> </div> <div class="qa-item"> <a href="https://thepharma.net/knowledgebase/what-role-does-regulatory-affairs-play" title="What Role Does Regulatory Affairs Play?">What Role Does Regulatory Affairs Play?</a> </div> <div class="qa-item"> <a href="https://thepharma.net/knowledgebase/why-are-clinical-trials-important" title="Why Are Clinical Trials Important?">Why Are Clinical Trials Important?</a> </div> <div class="qa-item"> <a 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