Comprehensive Clinical Quality Assurance Support
Audits
Gap Analysis
Training
Ensure your clinical trials and pharmacovigilance processes are fully compliant with global regulations.
- GCP Audits: Evaluate the quality and compliance of your clinical trials with ICH GCP guidelines.
- PV Audits: Assess the safety monitoring systems and processes in place to meet pharmacovigilance requirements.
- Vendor Audits: Verify that thi
Ensure your clinical trials and pharmacovigilance processes are fully compliant with global regulations.
- GCP Audits: Evaluate the quality and compliance of your clinical trials with ICH GCP guidelines.
- PV Audits: Assess the safety monitoring systems and processes in place to meet pharmacovigilance requirements.
- Vendor Audits: Verify that third-party service providers meet your quality and compliance standards.
Training
Gap Analysis
Training
Empower your team with expert-led, practical training tailored to your organization’s needs.
- GCP and PV Training: Equip your staff with the knowledge to maintain compliance and excel in audits.
- Inspection Readiness Training: Prepare your team to handle regulatory inspections with confidence and professionalism.
Gap Analysis
Gap Analysis
Inspection Preparation
Identify compliance gaps and improve your processes with our thorough assessments.
- Our gap analysis services provide a clear roadmap to address weaknesses in your clinical operations, SOPs, and quality management systems.
- Receive actionable recommendations to align with global regulatory standards.
Inspection Preparation
Inspection Preparation
Inspection Preparation
Navigate the complexities of regulatory inspections with our expert guidance.
- We assist with mock inspections, documentation reviews, and interview preparation to ensure you’re fully ready for regulatory authorities like the MHRA, EMA, and FDA, Gulf Health Council (GHC) Qatar Ministry of Public Health (MOPH) and Saudi Food and Drug Authority (SFDA)
Technical Writing
Inspection Preparation
Technical Writing
Ensure your documentation is clear, precise, and compliant with industry standards.
- SOP Development: We write and revise standard operating procedures (SOPs) to reflect current regulatory expectations and operational best practices.
- Regulatory Documentation: Support for clinical trial protocols, investigator brochures, and other essential documents.
Why Choose MSAQS?
- Tailored Solutions: Every organization is different. We adapt our services to fit your goals and challenges.
- Industry Expertise: With in-depth knowledge of ICH guidelines, GCP, and PV requirements, we deliver the highest standards of service.
- Comprehensive Support: From audits to training, we provide end-to-end solutions to ensure your success.
Partner with MSAQS
Whether you’re launching your first clinical trial, expanding your operations, or optimizing your quality systems, MSAQS is here to help.
Contact us today to discuss how our services can support your clinical quality assurance needs. Together, we’ll ensure compliance, improve efficiency, and enhance your organization’s success.