Oridin Group
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Regulatory consulting and strategic guidance

Expert Consulting in Clinical and Regulatory Strategy

Oridin Group specializes in guiding pharmaceutical and biotech organizations through the complexities of clinical development, regulatory submission, and quality systems. From pre-IND strategy to post-market compliance, we bring hands-on expertise and a track record of success across government-funded and commercial engagements.


- Consulting Services

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  • Clinical
  • Regulatory
  • Manufacturing
  • Strategy
  • Quality
  • Compliance
Clinical Trial Operations Clinical Trial Operations End-to-end clinical trial execution, including protocol development, site management, and data collection.
Regulatory Submissions Regulatory Submissions Preparation and submission of IND, NDA, and BLA filings in alignment with FDA requirements.
Tech Transfer & Scale-Up Tech Transfer & Scale-Up Support for process development, tech transfer, and scale-up to cGMP manufacturing.
Federal Market Access Strategy Federal Market Access Strategy Market planning for public-sector channels including VA, DoD, and national stockpiles.
cGMP Quality Systems cGMP Quality Systems Design and implementation of quality management systems for regulated environments.
Federal Contract Compliance Federal Contract Compliance Support for FAR, DFARS, Section 889, and other federal contracting requirements.

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Reach out for scientifically sound, market-ready guidance—delivered with precision and ingenuity.

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Email info@oridingroup.com

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