
Bridging Innovation and Regulatory Success
Navigating regulatory pathways can be one of the most challenging and time-consuming aspects of drug development.
Whether you're a university research team, an emerging biotech startup, or an established pharmaceutical manufacturer, ensuring regulatory compliance while accelerating drug development is critical to success.
Who We Support
How Parimer Helps
Regulatory Strategy & Compliance Support
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Comprehensive guidance on FDA, EMA, and global requirements
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Assistance with preclinical and clinical trial applications
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Risk assessment & regulatory gap analysis
Manufacturing & GMP Readiness
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Facility compliance audits & documentation
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GMP training & implementation strategies
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Vendor qualification & supply chain compliance
Submission & Approval Acceleration
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Preparing IND, NDA, BLA, and 510(k) filings
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Regulatory writing & dossier compilation
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FDA meeting preparation & response strategies