GMPriority Pharma facility achieves GMP status
We are proud to announce that GMPriority Pharma has achieved the prestigious Good Manufacturing Practice (GMP) status, certified by NQA. This significant milestone underscores our continued commitment to maintaining the highest standards of quality and safety in the research and manufacturing of innovative liposomal products.
What is GMP and Why is it Important?
Good Manufacturing Practice (GMP) is a system that ensures products are consistently produced and controlled according to quality standards. It is designed to minimise the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. Achieving GMP certification is a testament to a company’s dedication to quality management, rigorous process control, and continual improvement.
GMP covers all aspects of production, from the starting materials, premises, and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process.
At GMPriority Pharma, our journey to GMP certification began with a vision to set new benchmarks in the liposomal manufacturing industry. Our team embarked on this mission with a singular mindset for quality, innovation, and customer satisfaction.
Here are just some key steps we undertook to achieve this milestone:
1. Comprehensive Quality Management System (QMS):
We implemented a robust Quality Management System (QMS) that aligns with GMP requirements. This system ensures that every aspect of our manufacturing process is monitored, controlled, and continuously improved.
2. Rigorous Process Controls:
Our manufacturing processes are constantly reviewed and optimised to ensure consistency and reliability. We established stringent process controls to minimise variability and ensure the highest quality of our products.
3. Staff Training and Development:
Our employees underwent extensive training to understand and implement GMP guidelines. Continuous professional development ensures that our team stays updated with the latest industry standards and practices.
4. State-of-the-Art Facilities:
We invested in cutting-edge technology and state-of-the-art facilities to support our manufacturing processes. Our facilities are designed not only to meet but exceed GMP standards, providing a safe and controlled environment for product development.
5. Documentation and Traceability:
Detailed documentation and traceability underpin all our operations. We mandate every step of the manufacturing process is documented, providing transparency and accountability.
6. Regular Audits and Inspections:
Our commitment to quality is further reinforced by spot check internal audits and “surprise” inspections. These audits help us identify areas for improvement and guarantee continued compliance with GMP standards.
The Role of NQA in GMP Certification
NQA, a globally recognised certification body, played a pivotal role in our journey to GMP certification. NQA’s rigorous assessment process involved a thorough evaluation of our quality management systems, manufacturing processes, and compliance with GMP guidelines. Their certification is confirmation of our adherence to the highest standards of quality and safety.
What This Means for Our Customers and Partners
Achieving GMP status is not just an internal milestone; it directly benefits our customers by ensuring that every product manufactured by GMPriority Pharma meets the highest standards of quality, safety, and efficacy.
Our customers can have complete confidence in the consistency and reliability of our products, knowing that they are produced in a GMP-certified facility.
