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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
Available in English only
Implement a quality system tailored for you
Available in English only
We can help you build a quality system that is right for you and will allow you to effectively navigate the ever-changing world of quality compliance.
Available in English only
