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Confidently go to market with ongoing quality and compliance support
We can help you go to market with the
highest quality products that meet the
regulatory and compliance requirements
of your local communities, while also
being prepared for growth and sustained
success.
Use our risk assessment tool with audit
trail functionality and visibility to
gain actionable insights related to
updating and scaling up your
manufacturing processes, enhancing your
inspection readiness, and planning for
an impactful, continuous quality risk
management strategy.
- Commercial readiness: Leverage our deep understanding of global regulatory requirements, our robust quality assurance systems, and tried-and-true risk management strategies to give you the confidence to launch products and sustain them throughout the product lifecycle.
- Compliance and remediation: Tailor remediation plans designed to address your specific challenges, correct deficiencies, and prevent recurrence. Our training programs are focused on compliance and remediation practices to improve processes going forward.
Features and services
- Active pharmaceutical ingredients (APIs)
- Pharmaceuticals
- Biologics
- Medical devices - ISO 13485 / Medical Device Single Audit Program (MDSAP)
- Natural health products
- Cosmetics
- Compliance
- Audits
- Supply chain
- Validation
- Good manufacturing practice (GMP) fundamentals
- Medical device fundamentals
- ISO 13485:2016 / Medical Device Single Audit Program (MDSAP)
- Annual GMP training
- Preparing for a regulatory inspection
- Quality auditing
- Good documentation practices
- Supply chain and establishment licensing
