Your Bespoke Firm For Translational and pre-Clinical Drug Development

At PreClinIQ we hold your hand and pave the next steps while you focus on optimizing your lead candidate profiles. Our custom tailored services lets you be as hands off or as involved in the process as you like.

Our Scientific Services include

Finding the right CRO or partner

We specialize in personalized matchmaking, and tailoring our services to fit the unique research requirements and objectives of our clients. What distinguishes us is our ability to align these needs with the strengths and capabilities of different CROs or partners.

We take pride in our expansive network of reputed leaders in research sites across the US, Canada, and Europe that encompass and have experience in many disease indications and animal models. We capitalize on networking opportunities, industry events, conferences, and collaborations to stay updated on potential partners to constantly expand our capabilities.

Literature Deep Dive

Employing scientific teams with strong research backgrounds in the relevant therapeutic area.

Conducting in-depth literature reviews to understand the current landscape of research and potential gaps.

Provide comprehensive reports, summaries and references to help you kickstart your journey

Optimal Animal Model

Therapeutic Area Expertise:

Our team of experts understand the nuances of different disease models and their relevance. As part of our comprehensive service, we will assess and identify the advantages and limitations of various animal models.

Consultation Services:

Recommending the most suitable animal model based on scientific literature and industry standards.

Study Design and Execution

Our strength lies in scientific design expertise, where we craft preclinical studies tailored precisely to research objectives. We integrate best practices for data reproducibility and regulatory compliance, ensuring top-quality outcomes.

On your behalf, we will actively engage in every phase of a study: managing the logistics, MTAs, contracts, approvals, timelines, budgets, shipping, and resource allocation.

We also take the lead in overseeing the study design, revisions in consultation of our client, protocol writing, initiation and supervising execution, ensuring compliance, conducting site visits, audits, managing shipping and receiving of samples, handling documentation, and performing results, stats and analytics.

Data Interpretation and Next Steps

Our team of experts can adeptly handle all the downstream analytics and data interpretation. PreclinIQ possesses uses advanced analytics tools to interpret data and extract valuable insights from complex datasets. We offer strategic recommendations based on study outcomes, collaborating closely with clients to develop actionable plans and roadmaps for further research and development.

Regulatory Expertise

We also assist our clients with regulatory submissions and ensuring studies adhere to FDA, EMA, or other regulatory standards. Our team offers continuous technical support, addressing any issues that may arise during experimentation and providing troubleshooting solutions.

What We Do best

Understand your business and scientific needs.
Hold your hand and pave the next steps while you focus on optimizing your lead candidate profiles. (You can be as hands off or as involved in the process as you like).
Our team will meet with you to learn about your research goals and identify gaps and strengths in your research approach.
Our experienced team of scientists, and leading experts in the field work tirelessly in finding the right Contract Research Organization (CRO) or partner that fit your research needs.
We will survey the competitor landscape, do any literature deep dives and recommend the optimal animal model (or alternative additional ex vivo approaches to validate your in vitro results.
Once agreed upon, we can also reach out, get quotes, set up contracts, do site visits, vet the teams and be present during the study period to ensure optimal execution.
Next, the team will assist in designing studies, assisting in running the study, interpreting data, and identifying next steps as it is crucial for the successful progression of drug discovery.

Our Core Strengths

Pharmacology

Pharmacology is the study of how drugs interact with biological systems. In the context of drug development, this involves understanding the effects of a drug candidate on the body, including its mechanism of action, efficacy, potency, and potential therapeutic uses.

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Pharmacokinetics/ADME

Pharmacokinetics (PK) focuses on how the body processes a drug, including absorption, distribution, metabolism, and excretion (ADME). Understanding PK is crucial for determining dosing regimens and predicting drug behavior in humans.

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Toxicology

Toxicology focuses on the study of adverse effects of drugs and chemicals on living organisms. In drug development, toxicology studies are crucial for assessing the safety profile of a drug candidate.

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CMC & Formulations

CMC (Chemistry, Manufacturing, and Controls) and formulations focus on the chemical composition of the drug, its manufacturing process, and the final dosage form.

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Tailored solutions for your research needs

Unlock the potential of your research with our tailored solutions. At PreclinIQ, we understand that every research endeavor is unique, and we’re here to provide customized strategies to address your specific needs. From concept to execution, we deliver personalized solutions that drive your research forward, ensuring optimal outcomes and scientific excellence. With our expertise and commitment to innovation, you can trust us to partner with you in optimizing your research efforts, bringing your vision to life, and achieving your scientific goals.

Pharmaceutical and Biotechnology Companies

Pharma and biotech firms trust PreClinIQ for end-to-end preclinical support, from regulatory strategy development to IND submissions. Our consultancy empowers these companies to navigate complex regulatory landscapes, accelerate drug development timelines, and bring innovative therapies to market.

Contract Research Organizations (CROs)

For CROs, PreClinIQ offers expert regulatory guidance and preclinical study design services to ensure compliance with regulatory standards and optimize study outcomes. Our tailored solutions streamline processes, enhance efficiency, and drive success in preclinical research projects.

Academic and Research Institutions

Academic and research institutions can benefit from PreClinIQ’s comprehensive preclinical consulting services, which include study design, data analysis, and regulatory support. Our expertise aids in advancing scientific discoveries, securing funding, and translating research findings into impactful solutions.

Startups and Emerging Biotech Ventures

Startups and emerging biotech ventures rely on PreClinIQ for strategic guidance and operational support during the preclinical phase. Our tailored solutions address unique challenges, optimize resource allocation, and pave the way for successful preclinical development, laying a solid foundation for future growth and investment.

Your Bespoke Firm For Translational and pre-Clinical Drug Development

Our Scientific Services include

Finding the right CRO or partner

Literature Deep Dive

Optimal Animal Model

Study Design and Execution

Data Interpretation and Next Steps

Regulatory Expertise

What We Do best

Our Core Strengths

Pharmacology

Pharmacokinetics/ADME

Toxicology

CMC & Formulations

Tailored solutions for your research needs

Pharmaceutical and Biotechnology Companies

Contract Research Organizations (CROs)

Academic and Research Institutions

Startups and Emerging Biotech Ventures

let's collaborate on turning your innovative ideas into impactful breakthroughs.

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Key Areas We Can Help

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