Advancing Drugs

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   Preclinical Consulting?   Preclinical Project Management?

                         Contact us today to discuss your requirements

         Professional Services

  • Vendor Selection/Quotation Service
  • Project Management - GLP Toxicology
  • IND Submission Package Development
  • eCTD Filings

Preclinical services

We provide a variety of professional services to our clients at flat rate fees:  Vendor Selection and  Project Management Services (Up to complete end-to-end service for IND-enabling programs) and professional preclinical consulting for GLP toxicology studies in additional to Pre-IND meeting advisory & support, Preclinical Regulatory Assessments and Preclinical Study Design.   Our IND-enabling Gantt Chart for project management has over 2,800 individual tasks that need to be executed and coordinated with CROs & CMOs.

We have over 20 years of experience navigating the regulatory process for IND submission with the FDA. 

Call today to see if we offer a good fit for your goals.

 Call for a consultation  202-780-4988