IPA Montreal

SGS will be at the IPA 22nd Annual GMP Update | BPF Mise à jour, October 6 to 7, 2026, in Montréal, Canada. Visit us at Booth 1004 to discuss GMP compliance, regulatory readiness, audits, validation, training, and quality systems with SGS specialists. 

GMP compliance is not just about preparing for the next inspection. Organizations need systems that work consistently, respond to changing regulatory expectations, and identify gaps before they become larger compliance issues. SGS provides tailored support for pharmaceutical, OTC, cosmetics, and personal care organizations, from immediate regulatory needs to long-term quality system development. 


Strengthen GMP and Regulatory Readiness with SGS 

Whether you are preparing for an inspection, addressing a compliance gap, strengthening an existing quality system, or expanding your capabilities, our team can help with: 

 

• Regulatory Readiness and Remediation: Prepare for regulatory scrutiny with FDA mock audits, FDA inspection readiness training, 483 response, warning letter response, FDA remediation, and support for Health Canada, EU, TGA, and other regulatory requirements. 
  
  
• GMP Audits and Assessments: Identify gaps and evaluate readiness through pre-audits, gap assessments, second-party audits, supplier qualification support, and customized audit programs. 
  
  
• Quality Systems: Develop and strengthen GxP-GMP-GLP-GCP-GDP systems and SOPs while addressing data integrity and broader quality management requirements. 
  
  
• Qualification and Validation: Support commissioning, equipment and utility qualification, process validation, cleaning validation, computer system validation, method validation and verification, and water system design and validation. 
  
  
• Training: Build internal knowledge through standards training, internal auditor training, customized programs, and other virtual or on-site training designed around organizational needs. 
  
  
• Certification and Compliance Programs: Explore support for standards and programs including ISO 15378, GMP, ICH Q7, ISO 9001, WHO GMP for Pharma with 21 CFR Parts 210 and 211, and Health Canada audits. 
  
  
• Supply Chain and Due Diligence: Strengthen supplier oversight through qualification, due diligence, assessments, and SGS Compass supply chain risk management and compliance solutions. 

From Immediate Compliance Needs to Long-Term Improvement 

SGS can support organizations at different stages of their compliance journey. For teams facing an upcoming inspection or regulatory issue, that can mean targeted readiness and remediation support. For organizations building for the future, SGS can assist with quality systems, technical transfer, validation programs, equipment life cycle planning, stability planning and protocols, and annual product quality review support. 

Our approach is designed to help organizations understand where gaps exist, determine what needs attention, and put practical systems in place to support ongoing compliance. 

Visit Booth 1004 at the IPA 22nd Annual GMP Update | BPF Mise à jour to meet the SGS team and discuss your GMP, audit, validation, training, and regulatory compliance needs. 

For further information, please contact:

Alok Soni
Marketing and Sales Support Specialist
t: +1-437-349-0765