Pharma and Health
Our experience in document management in highly regulated environments allows us to address the challenges of the sector with solvency, providing knowledge, methodology and technology to ensure compliance and efficiency.
From data to compliance,
with traceability and control
Documentum for LifeSciences
Unlock the potential of your OpenText environment with expert support.
We help organizations in the Pharma and Life Sciences sector to optimize the use of Documentum for Life Sciences, ensuring that their document processes comply with the most demanding regulations and integrate with their workflows efficiently and securely.
- Compliance with FDA 21 CFR Part 11
- Improved traceability and productivity
- Seamless integration with quality and manufacturing processes
- Continued support and evolution of the environment
Clinical
Documentum for eTMF
We help you eliminate complexity and risk in the management of clinical trial documentation, ensuring traceability and regulatory compliance from study design to study closure.
Regulatory
Documentum for Research and Development
We facilitate the review, approval and control of regulatory documentation, speeding up processes and reducing errors in highly auditable environments.
Medical
Documentum for Quality and Manufacturing
Acompañamos a los equipos de calidad y producción en la gestión automatizada de la documentación crítica, mejorando la eficiencia, la agilidad y el cumplimiento.
Documentum for HealthCare
We connect clinical information for more agile and secure care.
We support hospitals and healthcare organizations in the implementation and evolution of Documentum for HealthCare, helping them to centralize critical information, digitize processes and improve patient data traceability in complex and regulated environments.
We automate the capture, organization and archiving of healthcare documentation, ensuring secure access, regulatory compliance and continuity of care.
Clinical archive
We securely manage different types of medical information, ensuring traceability, fast access, regulatory compliance and long-term data integrity.
Digital records
We transform physical and unstructured records into accessible digital information ready to be integrated with existing clinical systems.
Patient's vision
We facilitate a complete and integrated view of the patient, connecting dispersed data between clinical, administrative and diagnostic systems.
Interoperability
We implement standards such as HL7, FHIR and DICOM to ensure seamless communication between clinical, administrative and medical imaging systems.
Flow automation
We design automated processes that streamline information exchange, reduce errors and improve decision making in complex and highly regulated healthcare environments.