A Peek into Our Consultation Process

How AniLocus Collaborates

At AniLocus, we measure our success by the success of our clients. Whether your team is initiating preclinical studies, navigating clinical trials, or seeking regulatory guidance, we are committed to being your dedicated partner in achieving results.

Initial Assessment

We start by understanding your organization, project goals, and current challenges, ensuring a thorough grasp of your unique requirements.

Strategic Plans

Leveraging our experience, we collaboratively develop a strategic plan tailored to your project's needs, identifying key milestones and timelines.

Scientific Support

Our team of experts actively engages in providing scientific and technical support, ensuring that your research benefits from the depth of our knowledge.


Open lines of communication are essential. We maintain transparency throughout the process, keeping you informed and involved in decision-making.

Contact Us

Ready to elevate your research to new heights? Contact us today: 

    Primary Contact/Sponsor


    Full Name*:


    Position Title*:



    Sponsor Organization/Institution*:

    Sponsor Website:

    Project Details

    Type of Study*:

    Other (Specify):

    Drug Development Phase*:

    Specific Objectives/Outcomes*:

    Study Requirements

    Animal Model*:

    Other (Specify):

    Number of Groups*:

    Sample Size (Per Group)*:

    Study Duration/Timeline*:

    Budget Constraints (if any) *:

    Additional Information

    Any Specific Assays or Tests Required*:

    Regulatory Requirements*:

    Terms and Conditions

    Terms of Service and Agreement*:

    Learn More About Our Services

    Therapeutic Areas

    Preclinical Plans

    Scientific Writing

    Medical and Scientific Communications

    • Abstracts
    • Blog Content Marketing
    • Manuscript Submission Management
    • Manuscripts Writing & Editing
    • Posters
    • Press Releases
    • Scientific Presentations
    • Webinar Content Marketing
    • White Paper Content Marketing

    IND Preparation

    • Pre-IND FDA Meetings
    • IND Writing & Submission
    • Management of IND Enabling Studies
    • Pharmacology Data Analysis (TK, PK, PK/PD)
    • Pharmacology Modeling & Simulation

    GLP Compliance

    • Master Study Schedule Planning
    • Quality Assurance
    • Standards/Guidances Adherence
    • Test/Control Article Characterization
    • Equipment Standardization & Maintenance 


    • DEA License Application Preparations (Controlled Substances Use in R&D)
    • Partial Tax Exemption Certificates for R&D
    • Grant Review (CIRM, SBIR)