CANARITECH is a leading Contract Research Organization (CRO) focused on delivering high-quality clinical research and regulatory solutions across Latin America. We combine global standards with deep regional expertise to support pharmaceutical, biotechnology, and medical device companies at every stage of development.

Our team works closely with clients to ensure clarity, compliance, and efficient execution—transforming scientific challenges into actionable results.

Use the form below to contact our team and start a conversation about your project.

    CALL US 1-677-124-44227
     

    Services

    Comprehensive clinical, regulatory, and biotechnology solutions designed to support innovation and ensure compliance across Latin America.

    • Clinical Trial Management

    • End-to-end management of Phase I–IV clinical trials, including protocol design, site selection, patient recruitment, monitoring, and study closeout.
All operations follow Good Clinical Practice (GCP) and international standards.

    • Pharmacovigilance

    • Comprehensive safety monitoring during clinical and post-marketing phases:

      • Adverse event reporting
      • Safety risk management plans
      • Regulatory submissions (COFEPRIS, FDA, EMA)
      • Support during audits and inspections

    • Biostatistics

    • Robust statistical study design, advanced data analysis, and ICH-compliant reporting to support strong scientific conclusions.

    • Data Management

    • Secure, GCP- and GDPR-compliant systems for:

      • Database creation
      • Data cleaning
      • Data validation
      • Integration and preparation for analysis

      Ensuring accuracy, traceability, and data integrity.

    • Regulatory Affairs

    • Strategic regulatory planning and execution for:

      • Medicines
      • Biologics and advanced therapies
      • Medical devices
      • Food supplements
      • Cosmetics

      Support includes classification, dossier preparation, submission, regulatory interactions, and post-approval requirements.

    • International Trade (Foreign Trade)

    • Solutions for companies engaging in cross-border operations:

      • Customs compliance
      • Free Trade Agreements (USMCA, ALADI, Pacific Alliance, and more)
      • MIMMEX, PROSEC, AEO certification
      • Logistics regulatory consulting
      • Tariff classification and tax optimization

    • Intellectual Property

    • Protection of scientific and commercial innovation:

      • Trademarks
      • Industrial designs
      • International patents (PCT)

    • Technical Consulting

    • Expert support for:

      • GMP/GxP compliance
      • Biotechnology process development
      • Facility and clean room design (ISO 14644)
      • Machinery acquisition
      • Supplier evaluation and qualification

    • Startups

    • Support for health-sector startups:

      • Strategic guidance
      • Technical feasibility evaluations
      • Investor preparation and capital-raising support

    REGIONAL COVERAGE

    CANARITECH operates across the entire Latin American region, with expertise in navigating country-specific regulatory frameworks.
    Our operations comply with:

    • Good Clinical Practice (GCP)

    • International Council for Harmonisation (ICH)

    • Helsinki Declaration (2013)

    • National regulatory authorities (COFEPRIS, ANVISA, INVIMA, ANMAT, ISP, MINSA, DIGEMID, FDA alignment)

    We leverage regional diversity and strong investigator networks to accelerate recruitment and deliver high-quality results.