Our Services

General Consulting

VJO Canada offers comprehensive drug development consulting, supporting virtual, small, and mid-sized biotech companies with expert guidance from early-stage strategy to regulatory submission. Our multidisciplinary team brings decades of experience to every engagement—ensuring your development program is aligned, efficient, and built for success.


We provide tailored consulting across key areas:



  • Outsourcing, Project Management & Monitoring – Oversight of studies across continental and international regions, led by board-certified multidisciplinary Subject Matter Experts (SMEs)


  • Product Development & Registration Strategies – End-to-end planning to support regulatory approvals in key global markets


  • Scientific & Medical Writing – Protocols, regulatory documentation, and communications written by experienced professionals


  • Nonclinical & Clinical Development Support – Integrated planning and execution across both preclinical and clinical phases


  • Bioanalytical, Analytical & Immunological Expertise – Guidance in assay development, validation, and sample analysis


  • Chemistry & Manufacturing (CMC) – Strategic input on drug substance and drug product development, from formulation to scale-up


  • Investigator’s Brochures – Preparation and updates for regulatory and clinical stakeholders


  • Data Review & Gap Analyses – Critical assessment of existing data to identify deficiencies and define mitigation strategies


  • Scientific & Regulatory Due Diligence – Independent evaluations to support partnerships, licensing, and investor relations


  • Investment Strategy Support – Assistance with in-licensing, technology transfer, and funding strategies (dilutive and non-dilutive)


Whether you’re refining your development plan or preparing for agency engagement, VJO Canada acts as your strategic ally—providing focused insight, operational excellence, and trusted guidance every step of the way.