Scientific, Regulatory & Quality

Discovery Sciences

Scientific rigor to drive molecule optimization and clinical readiness.

Advance your molecule with speed and precision.

Candidate selection is the most important discovery milestone—it marks the end of molecule optimization and the foundation for clinical success.

Syner-G helps innovators overcome barriers in molecule optimization and lead development. Our focus is on enabling data-driven, scientific decisions that accelerate the advancement of compounds into successful clinical candidates.

Challenges we can help solve:

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Client Return Rate

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Assets Supported

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INDs Filed

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 NDAs / BLAs Filed

Trusted partner with hundreds of INDs filed.

We help clients ensure a seamless transition between discovery and development—enabling quicker IND filings and clinical success.
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Our Approach

Driving discovery programs forward.

Our goal is to fast-track discovery, improve quality, mitigate development risks, and prepare candidates for clinical success.

By uniting deep scientific expertise, proven methodologies, and a trusted partner network, we help programs move faster, with stronger foundations.

  • Small Molecule Expertise: small molecule design and synthesis to ensure each candidate is optimized for both science and speed
  • Large Molecule Expertise: we help you address key challenges early to strengthen your program’s success, from design and engineering to manufacturability assessment
  • A Complete, Integrated Path: from small molecules to biologics, from discovery through preclinical, our integrated support increases the probability of advancing the right candidates with confidence

A complete, fully-integrated solution.

Our integrated approach connects discovery, CMC, regulatory, medical writing, and quality from early development through approval—reducing handoffs, aligning teams, and helping you avoid costly delays.
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CMC Strategy & Development

An integrated approach that ensures phase-appropriate control strategies and sets your asset on the most efficient course toward approval.

Regulatory Strategy

From IND and CTA submissions through pivotal trials, approval, and beyond—we help you avoid rework and keep momentum throughout your program’s lifecycle.

Medical Writing

Every protocol, clinical study report, and submission module is crafted with regulatory reviewers in mind—communicating complex data with precision, consistency, and credibility.

Quality & Compliance

Scalable quality systems that match the pace of innovation, support regulatory compliance, and enable smooth program advancement.

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Let's move from science to success.

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