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To better assist you with your request, please choose a research area provided by VeNaV Consulting. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.

In Vitro Assay Development

Develop innovative assay and screening methods outside a living organism to enable a wide range of pre-clinical activities.
Publication Writing

Make clear and accurate presentations of scientific and technical data.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Site Selection

Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Small Molecule Drug Development Consulting

Request consulting services related to small molecule development.
Phase 1-3 Studies

Design phase 1-3 studies that seek to identify if a drug is safe, effective, and more efficient than other available treatments on the market.
Discovery Data Management

A process that includes acquiring, validating, storing, protecting, and processing required data to ensure the accessibility, reliability, and timeliness of the data for its users.
Portfolio Management

Manage a portfolio of projects in early-stage drug discovery and provide factors that determine the success of the proposed portfolio.
Target Validation Consulting

Help to demonstrate that modification of target activity has potential therapeutic benefits.
Target Product Profile (TPP)

A sponsor prepared document which summarizes the drug development program that is described in terms of the labelling concepts. This profile is a communication method used between the FDA and sponsor which can be used throughout all stages of the drug development process, from Pre-investigational, to NDA.
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