Our commitment to excellence is reflected in our robust Quality Management Systems (QMS) frameworks, designed to ensure the highest standards of quality and compliance across your pharmaceutical development projects. At Syner-G, we understand the critical importance of quality management in the pharmaceutical industry, and we are dedicated to providing systems that not only meet but exceed global regulatory standards.
What is a Quality Management System?
A QMS is a formalized system that documents the structure, responsibilities, and procedures required to achieve effective quality management. At Syner-G, the QMS is the backbone of our operation, ensuring consistency and improvement in all aspects of our services. The system comprises various key components including the Quality Manual, Quality Policies, and Standard Operating Procedures (SOPs), which are tailored to meet the specific needs of our clients and regulatory requirements.
Core Components of Our QMS
Quality Manual
Our Quality Manual serves as the cornerstone of our QMS. It outlines our quality philosophy, the organizational structure, and the specific responsibilities of each position in relation to quality. This document acts as a guide for our employees and clients, providing a clear path to compliance and excellence. Additionally, it is dynamically tailored to align with the specific phase and complexity of each client’s program, ensuring a bespoke approach to quality management.
Quality Policies
The Quality Policies at Syner-G establish the fundamental principles that all our processes and operations adhere to. These policies support our mission to deliver high-quality pharmaceutical services and are regularly reviewed and updated to incorporate the latest regulatory changes and industry best practices. Our flexibility allows us to adapt these policies to better suit the varying needs of our clients’ diverse projects.
Standard Operating Procedures (SOPs)
Our SOPs provide detailed, step-by-step instructions designed to carry out operations that are consistent and efficient. They ensure that all personnel perform tasks uniformly and are crucial in maintaining high standards of quality and regulatory compliance. We develop these procedures with scalability in mind, customizing them to cater to the unique requirements of different phases of clinical and manufacturing processes.
Implementation and Training
Successful implementation of our QMS is achieved through comprehensive training programs that are designed to thoroughly acquaint staff with the QMS components and are customized based on the specific needs of the project and the team involved. Our GMP (Good Manufacturing Practice) training ensures that all team members are up-to-date on the latest industry standards and procedures, and are well-prepared to address the unique challenges of each project.
Continuous Improvement and Compliance
At Syner-G, continuous improvement is embedded in our QMS. We employ periodic reviews and revisions of our systems and procedures to adapt to new challenges and changes in the regulatory landscape. Our proactive approach includes regular internal and external audits, which help to identify areas for improvement and ensure compliance with all applicable laws and regulations. This commitment to ongoing enhancement is critical as we tailor our services to meet the evolving needs of our clients throughout the lifecycle of their programs.
Benefits of Our QMS
Consistency
Our QMS ensures that all project activities are conducted in a consistent manner, leading to reliable and predictable results.
Compliance
With our comprehensive understanding of regulatory requirements, our QMS is designed to ensure that all operations are compliant with international quality standards.
Efficiency
By standardizing operations, our QMS minimizes errors and increases efficiency, reducing costs and speeding up time to market for pharmaceutical products.
Client Confidence
Our robust QMS frameworks build client trust and confidence, demonstrating our commitment to quality and compliance.
At Syner-G, we are proud
to offer a QMS
That is not only compliant with international standards but also a step ahead in promoting quality assurance and regulatory compliance. Partner with us to ensure that your pharmaceutical projects are managed under the highest standards of quality and professionalism.