Nonclinical Development & CMC

PPD® Laboratories offers specialized nonclinical pharmacology/toxicology and chemistry, manufacturing and controls (CMC) consulting services globally, which can be provided separately or as part of a fully integrated development program. Our dedicated nonclinical and CMC teams work with you to develop the strategy for your product and to design and execute a CMC/nonclinical program that is optimized to support your clinical development and regulatory plans.

Our expert pharmacology/toxicology and CMC consultants provide a wide range of services across the pharmaceutical development spectrum, including:

  • Small molecules
  • Biologic products, including biosimilars
  • Vaccines
  • Generic drugs
  • Over-the-counter (OTC) and consumer health products
  • Medical devices
  • Advanced therapy medicinal products, including genetically modified organisms

Through close collaboration with PPD’s clinical pharmacology team and GMP, bioanalytical and discovery pharmacology labs, we provide complete support for your product throughout global development, from product discovery through post-approval lifecycle management.

CMC Regulatory

PPD® Laboratories chemistry, manufacturing and controls (CMC) group provides scientific and regulatory expertise in all areas of CMC development.


PPD® Laboratories Pharmacology/toxicology consultants work closely with pharmacokineticists to design and implement comprehensive nonclinical plans to enable successful product development.

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