Our Pharmaceutical
Capabilities
Sortis Pharma provides integrated pharmaceutical capabilities focused on formulation development, manufacturing support,
quality systems, regulatory documentation, and global supply coordination. Our work supports partners across
different stages of the pharmaceutical product lifecycle.
Structured pharmaceutical development services
supporting quality and compliance
Finished Dosage Manufacturing Support at CMO site
Sortis Pharma supports finished dosage manufacturing through coordinated operations and quality-aligned processes. Activities are focused on maintaining consistency, reproducibility, and compliance across manufacturing stages.
Quality Assurance & Quality Control
We operate structured quality systems that support:
- Quality assurance frameworks
- Quality control testing coordination
- Documentation accuracy and traceability
- Compliance with applicable regulatory standards
Quality activities are integrated across development, manufacturing, and supply operations.
Regulatory Documentation & Compliance Support
We provide regulatory documentation support aligned with product development and manufacturing activities. This includes preparation and organization of documentation required to support regulatory review and market-specific requirements.
Global Supply & Distribution Coordination
Sortis Pharma supports global supply and distribution coordination through structured planning, partner alignment, and adherence to applicable regulatory and quality requirements. Our approach focuses on maintaining consistency across markets while accommodating regional regulatory, logistical, and documentation needs.
We work closely with distribution partners to support reliable supply across international markets. Our focus remains on consistent quality, clear coordination, and long-term supply continuity.
Looking for a Trusted Pharmaceutical Partner?
Let’s discuss how our pharmaceutical capabilities can support your requirements.