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EU GMP & ICH Certified

Patient Support Programs & Research Solutions

Compliance-Driven Patient Support & Regulatory Operations Across EU & MENA

  • 15+ Years in Regulatory & Market Access
  • ISO 27001 Certified Data Infrastructure
  • CNDP-Approved PSP Operator in Morocco

99.8%
Patient Satisfaction
5+
EUROPE & MENA Countries
15K+
Patients Supported
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Trusted Partners

Partnering with Industry Leaders

  • Collaborating with Global pharmaceutical manufacturers, Biotech companies, Medical Device firms, CROs seeking local execution partner.


Boehringer Ingelheim logo
Cipla logo
Partner logo
Pharmaprom logo
Amgen logo
Pierre Fabre logo
Boehringer Ingelheim logo
Cipla logo
Partner logo
Pharmaprom logo
Amgen logo
Pierre Fabre logo
Our Services

Comprehensive Healthcare Solutions

From regulatory strategy to patient safety, we provide end-to-end pharmaceutical and medical device support 

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Patient Support Programs

Design, implementation, and governance of branded and non-branded PSPs fully aligned with:

  • Local pharmacovigilance obligations
  • Data protection laws (GDPR, CNDP)
  • Sponsor SOPs
  • 24/7 Support Hotline
Science, teamwork and scientist with tablet in laboratory for communication, pharmaceutical review or planning.

Clinical Research

Operational Support for Interventional & Non-Interventional Studies

  • Phase I-IV trial Monitoring
  • Site feasibility & start-up
  • Data Management & Analysis
  • NTA (Non-Trial Activity) management
A diverse group of professionals in a modern office setting engaged in a collaborative business meeting.

Regulatory Consulting

Expert guidance for navigating regulatory requirements across MENA markets, from strategy to approval.

  • Market Authorization Strategy
  • Product Submission & Registration
  • Health Authority Liaison (MENA)
  • Lifecycle & Compliance Management
15+ Years of Excellence

MEA STUDIES HEALTH

Diverse healthcare professionals in uniforms and lab coats showcase teamwork and unity within a bright contemporary setting, symbolizing cooperation, professionalism, and a positive work atmosphere.
15K+
Patients
99.8%
Satisfaction
25+
Studies
8+
Countries

Certifications & Recognition

ISO 27001
GCP Compliant
CNDP Approved
GDPR Compliant

MSHEALTH is a Morocco-based regulatory and health operations company supporting pharmaceutical and MedTech manufacturers across EU and MENA

Founded by professionals with 15+ years of experience in regulatory affairs, pharmacovigilance, and patient engagement, MSHEALTH operates under a structured Quality Management System aligned with EU GMP and ICH standards.

Research Excellence

Advanced clinical research methodologies with proven track record

Regulatory Mastery

Deep expertise in MENA healthcare regulations and compliance

Patient-Centric Approach

Every solution designed with patient outcomes as the primary focus

Global Standards

International best practices adapted for regional healthcare needs

Regulatory Excellence

Safety & Regulatory Affairs in MENA

Deep local expertise combined with international standards to navigate complex regulatory landscapes.

Regulatory Strategy

Comprehensive regulatory pathway planning and market authorization support across MENA markets.

  • Market authorization dossiers
  • Regulatory intelligence & gap analysis
  • Product labeling & artwork review
  • Post-approval variations management

Safety & Pharmacovigilance

End-to-end pharmacovigilance services ensuring patient safety and regulatory compliance.

  • QPPV & local safety representatives
  • Adverse event reporting & case processing
  • PSUR, RMP & signal detection
  • Safety audits & inspections readiness

Regional Partnership Network

Strategic local partners across MENA ensuring seamless regulatory execution.

  • Local regulatory representatives
  • Authority liaisons & submissions
  • Country-specific compliance support
  • Market access strategy & execution
15+
Years of experience
15k
Lives Impacted
50+
Regional Consultants
24/7
Regional Support
Quality & Compliance

Governance & Quality Framework

Our governance structure ensures the highest standards of quality, safety, and regulatory compliance across all operations.

Internal SOP System

Standardized operating procedures ensuring consistent quality and compliance across all departments and processes.

CAPA Management

Comprehensive Corrective and Preventive Action system to address deviations and implement lasting solutions.

Risk Assessment Process

Systematic identification, analysis, and mitigation of risks to ensure patient safety and product quality.

Data Hosting & Encryption

Secure, encrypted data storage with HIPAA-compliant hosting ensuring maximum protection of sensitive information.

Vendor Qualification

Rigorous vendor assessment and qualification process ensuring all partners meet our strict quality standards.

Audit & Inspection Readiness

Continuous readiness for regulatory inspections with comprehensive documentation and self-audit programs.

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Get in Touch

Contact MS Health

Let's discuss how our solutions can revolutionize your healthcare delivery and improve patient outcomes across the MENA region.

Send Us a Message

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