KEY ASPECTS OF OUR GLP STUDY SERVICES
Compliance with GLP Standards
We ensure that all aspects of our GLP studies adhere to international GLP standards. This includes proper study planning, execution, monitoring, recording, archiving, and reporting.
Study Design and Protocol Development
Our experts assist in designing studies and developing detailed protocols that meet specific research objectives while ensuring GLP compliance. This includes identifying the appropriate study model, methods, and controls.
Quality Control and Assurance
We implement stringent quality control and assurance procedures throughout the study to ensure data accuracy and reliability. This involves regular monitoring and audits of the study process and documentation.
Data Management and Reporting
Our services include comprehensive data management, from collection and analysis to reporting. We ensure that data is accurately recorded, analyzed, and reported in a manner consistent with GLP requirements.
Facility and Equipment Management
We maintain high standards in facility management and equipment calibration, ensuring that the laboratory environment and tools are conducive to GLP-compliant studies.
Staff Training and Expertise
Our team comprises well-trained and experienced professionals knowledgeable in GLP principles and practices. Continuous training is provided to keep our staff updated on the latest GLP standards and techniques.
WHY CHOOSE MDS FINLAND FOR GLP STUDIES?
Expertise in GLP Compliance
Our team’s expertise in GLP ensures that your studies meet all necessary regulatory and quality standards.
Tailored Study Designs
We customize study designs to meet your specific research needs while ensuring compliance with GLP standards.
Comprehensive Service Offering
From study design to data reporting, our comprehensive GLP study services cover every aspect of your pre-clinical research needs.
ENSURING RELIABLE AND COMPLIANT PRE-CLINICAL STUDIES
MDS Finland’s GLP study services are essential for achieving reliable, high-quality pre-clinical data. Our adherence to GLP standards plays a critical role in the successful progression of medical devices and pharmaceuticals through the development pipeline
