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Analytical testing

Rooted in long-standing expertise, we deliver precise, consistent results and guidance at speed.
Analytical testing

Comprehensive GMP testing expertise

Our lab infrastructure and data systems are engineered for speed and precision, enabling more considered, confident, and compelling decisions.

Multifaceted molecular expertise

  • Small Molecules
  • Biologics
  • Nucleic acids
  • Novel products

Small Molecules

Despite the rise of biologics, gene therapies and cell-based medicines, small molecules remain one of the most important therapeutic modalities in drug development. Our teams have decades of experience in the development of these cost-effective and stable therapies for any number of indications including oncology, cardiovascular, neurology, immunology, and rare diseases.

Biologics

Biologics, which include any number of large molecules, such as recombinant proteins, monoclonal antibodies, ADCs, and gene/cell therapies, have become one of the most significant classes of drugs in modern medicine. Our scientists are experienced in the development and commercialization of this important, ever-evolving area to take advantage of their high target specificity, ability to treat previously untreatable diseases, and often long duration of action.

Nucleic acids

Nucleic acids, which are the building blocks of DNA and RNA, have become one of the most transformative therapeutic modalities in modern pharma. Unlike small molecules or biologics that interact with proteins, nucleic acid–based drugs can modulate gene expression directly, enabling entirely new ways to treat or even cure disease.

Our diverse experience spans chemically synthesized oligonucleotides (e.g., ASO, siRNA, aptamer, sgRNA, PMO/PPMO, etc.) as well as larger nucleic acid polymers produced by biological processes, such as in vitro transcription (e.g., mRNA, tRNA, circular RNA, etc.) or bacterial expression (e.g., plasmid DNA).

Novel products

Push the boundaries of what’s possible in drug development with our forward-looking partnership to help navigate uncertainty. We apply diverse molecular experience with proven processes and emerging technologies to advance your product toward clinical phases.

Our team specialized numerous carriers to safeguard your API from environmental influences while optimizing pathways to the targeted cell and tissue types. Some of these include virus like particles (VLPs), viral vectors, adeno-associated virus (AAV), lipid nanoparticles (LNPs), and antibody-drug conjugates (ADCs).

CDMO services built for progress

From early development through to regulatory approval, our capabilities are designed to keep you moving with clarity and confidence. We combine analytical strength, thoughtful problem-solving and practical manufacturing expertise to support your path from discovery to delivery.

The safe and the smart choice

Pace® Life Sciences offers the reliability of a respected, established operation, with the flexibility of a mid-sized CDMO. Our teams provide practical insight, scientific precision, and dependable oversight, supported by a connected network of GMP-compliant facilities.

  • A significant U.S. footprint with specialized capabilities
  • Experienced teams who stay engaged and accessible
  • Scientific rigor paired with dependable delivery
  • A consultative culture focused on collaboration

Get in touch

Whether you’re shaping early plans or preparing to scale, our teams are here to help you move forward with clarity and confidence. Start the conversation and we’ll get back to you quickly.