Bringing OTC drugs and Natural Health Products (NHPs) to market comes with constant pressure—tight timelines, evolving regulations, and the need to ensure consistent product quality. Any gap in testing or compliance can delay approvals, disrupt supply, and impact consumer trust. Our team of experts in Toronto provide end-to-end GMP testing solutions for OTC and NHP products—accelerating the development to commercialisation journey with confidence.

Reliable data. Regulatory confidence. Scalable support.

From raw materials to finished products, we deliver comprehensive analytical services designed to verify identity, potency, purity, and safety under strict GMP conditions. Our team works with you to streamline testing strategies and documentation, ensuring your program remains efficient, compliant, and audit-ready.

Full lifecycle support for diverse product types We support a broad range of materials and formulations, including:

• Substances and raw materials
  • Active pharmaceutical ingredients (APIs)
  • Medicinal ingredients for NHPs
  • Excipients and inactive components
  • Botanical and naturally-sourced materials
  • Incoming material qualification and release testing
• Finished products
  • OTC drug products and NHPs
  • Solid, semi-solid, and liquid dosage forms (capsules, tablets, syrups, suspensions)
  • Non-sterile formulations
  • Stability and shelf-life programs

Testing designed to meet your timelines and requirements

Our laboratories operate with high capacity and flexible scheduling, enabling us to support both large-scale release programs and smaller development projects without compromising turnaround times.

We deliver a full range of analytical and microbiological testing services, including:

• Identity, potency, and purity testing
• Assay and content uniformity
• Dissolution and disintegration
• Impurity and degradation profiling
• Microbiological evaluation
• Stability studies (long-term, accelerated, intermediate)
• Method verification, transfer, and validation 

Stay aligned with complex regulatory requirements 

Navigating OTC and NHP regulations requires precision and expertise. Our services are designed to support compliance with:

• Health Canada requirements for OTC drugs and NHPs
• Good Manufacturing Practices (GMP)
• Product and site licensing requirements
• Lifecycle management from development through post-market support 

A testing partner that adapts to your needs

You need a partner who understands your production pressures and regulatory challenges. Our experienced teams combine scientific expertise with operational flexibility to:

• Maintain consistent product quality across batches
• Scale testing as your program grows
• Meet aggressive timelines without compromising compliance
• Generate accurate, defensible data for regulatory submission

Get in touch

With deep experience across OTC and NHP product categories, we reduce risk, streamline approvals, and deliver safe, high-quality products to market faster.

Contact us