What consulting services do you offer for radiopharmaceutical development?

RPT Labworks provides strategic consulting for method development, experimental design optimization, data analysis and interpretation, and preclinical IND support. Our experts help navigate regulatory requirements and optimize your development pathway to accelerate time to clinic.

When should I engage a radiopharmaceutical consultant?

Engaging a consultant early in development helps avoid costly mistakes and optimize your pathway. Key moments include: selecting between targeting vectors, designing preclinical study packages, preparing for IND submission, or when encountering unexpected results that require expert interpretation.

What is included in IND support services?

IND support includes guidance on preclinical study design to meet FDA requirements, data package organization, dosimetry calculations for human dose projection, and review of chemistry, manufacturing, and controls (CMC) documentation for radiopharmaceuticals.

Can you help with study design for novel targeting vectors?

Yes, we specialize in designing studies for novel radiopharmaceuticals including small molecules, peptides, antibodies, and emerging modalities. Our team has experience across dozens of target-ligand combinations and can recommend optimal study designs based on your vector's properties.

Consulting

Strategic guidance for navigating the complex landscape of radiopharmaceutical development. From early-stage method development to IND-enabling studies, our experts help you make informed decisions that accelerate your path to the clinic.

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