Quality, reliability, growth – all for your health
SPS Pharma commits to the international standards in pharmaceutical quality, ensuring patients receive safe and effective medicines.
Our Quality Management System is founded on the quality principles of ISO 9001
This approach allows us to ensure that our medicines align with the highest standards of safety and efficacy, building trust and satisfaction among our clients while supporting patient health.
We ensure alignment with all regulatory requirements, including GxP standards and ISO 9001. This guarantees that every step of our operations, from procurement to transportation, meets international quality standards.
Our Quality Management System (QMS) is a set of interrelated management elements that direct and control the company’s activities. This system extends to all departments, processes that may affect the quality of medicinal products.
We conduct thorough validation and verification of our processes and equipment to ensure their reliability and compliance with standards. This includes testing equipment, quality control systems, and IT infrastructure.
The risk management process comprises systematic actions aimed at coordinating, facilitating, and making informed decisions concerning quality. We perform hazard identification, risk analysis and evaluation of their impact, and implement risk mitigation measures.
Our employees participate in ongoing training and workshops to remain informed about the latest standards and technologies in pharmaceutical quality. We support the professional growth of our staff to uphold high standards.
We continuously work on improving our processes and Quality Management System. Through regular internal audits, data analysis, and the implementation of innovations, we aim to consistently improve the quality of our services.
Ensuring information security and data integrity is an integral part of our system. We use advanced technologies to protect the information and data of our partners and patients.
We highlight the importance of proper documentation practices
We ensure the reliability and security of our services due to our systematic approach to documentation, which form the foundation of our reputation and successful cooperation with international partners.
Proper documentation practices are critically important for ensuring the quality and safety of medicines at all stages of supply chain.
We conduct continuous monitoring of temperature conditions during the storage and transportation of medicines. Our automatic temperature reading systems provide continuous data recording, allowing for the immediate detection of any deviations from the established limits. Our automated temperature and humidity control system guarantees data retention and archiving, and issues alerts for deviations from predetermined storage conditions.
Any incidents that arise during the storage or transportation of medicines are documented in accordance with GxP standards. We conduct thorough investigations to determine the causes of incidents, including the collection of all necessary data, testimonies, and situation analysis. The investigation documentation includes all stages, from the detection of the incident to the implementation of corrective actions.
Our quality management system ensures proper documentation of all corrective and preventive actions (CAPA). Each incident investigation is concluded with the development and implementation of corrective actions to prevent repetition in the future. All CAPA measures are documented with a detailed description of the issue, the actions taken, and the results.
Wide range of services for efficient supply chain management
We offer a variety of services for pharmaceuticals and medical products supply. By using advanced technologies and transparent partnership terms, we ensure safe, timely, and high-quality delivery. Our goal is to support your business with reliability and professionalism at every stage.
Our logistics services are developed to maintain the quality and safety of pharmaceutical products.
We offer our customers a wide range of clinical materials intended to support clinical studies throughout the entire trial process.
We address patient needs with customized solutions to improve effectiveness throughout the entire clinical trial process.
