Driving Pharmaceutical Excellence Across Manufacturing, Quality, and Compliance
ALTEN Technology helps pharmaceutical companies optimize manufacturing, quality, and compliance across critical operations. With expertise in automation, validation (CQV/CSV), and manufacturing systems—supported by global CRO capabilities—we enable faster, more efficient paths to market.
Automation
Automation enhances efficiency, accuracy, and reproducibility in Pharmaceuticals by streamlining manufacturing and quality processes.
- Conceptualization, design, build, and integration of automated systems
- Validation and installation of production lines for smooth startup
- Custom and off-the-shelf equipment integration
ALTEN Technology brings years of experience in automated production line development, ensuring optimized, compliant, and reliable operations.
Manufacturing
(Includes Design & Installation)
Manufacturing in Pharmaceuticals requires precision, compliance, and adherence to GMP standards. ALTEN Technology supports the entire process, from design and installation through production and packaging.
- Expertise in regulated production environments
- Full support for custom equipment design, integration, and installation
- Turn-key program management or targeted consulting support
Our engineers and quality teams ensure safe, effective, and high-quality output across facilities.
Quality Assurance
Compliance & Deviation Management
Quality Assurance safeguards consistency and compliance throughout product lifecycles.
- Development and oversight of QA systems and processes
- Support for compliance audits and deviation management
- Testing, validation, planning, and execution
Our Quality teams are experts in global regulatory standards, ensuring products meet safety, efficacy, and reliability requirements.
Validation
CQV & CSV Services
Validation is critical to maintaining GxP compliance and product integrity. ALTEN Technology provides end-to-end support across:
- Commissioning: Ensuring equipment meets design and user requirements
- Qualification: Verifying equipment, systems, and software meet specifications
- Validation: Documenting that processes consistently produce compliant products
- Computer System Validation (CSV): Ensuring IT systems are reliable, accurate, secure, and compliant
Our engineers and project managers provide expertise across worldwide regulatory requirements to ensure safe, validated operations.
Contract Research Organization (CRO)
Through our solution company Aixial, ALTEN Technology provides full CRO support to accelerate clinical development.
- Pre-clinical and clinical trial management
- Regulatory affairs and data management
- Seamless integration from CRO to manufacturing and commercialization
With Aixial, we enable parallel execution of CRO and production planning, reducing time-to-market and ensuring a unified, well-managed program.
Areas of Expertise
- CQV
- Deviation Management
- Automation
- Process Improvement
- Equipment Qualification
- FAT
- Technical Documentation
- Quality Assurance
- Engineering
- Validation
- GXP Compliance
- Reliability
Services
