Why Choose Us
At SURARK, we pride ourselves on delivering excellence in pharmaceutical packaging solutions, focusing on transparency, precision, and customer satisfaction. Our commitment to quality and efficiency is evident in every aspect of our operations.
Quality Management
To guarantee that all electronic data is handled precisely, avoiding mismanagement and improving documentation transparency, we make use of a electronic Quality Management System (QMS). At SURARK, we utilize an Electronic Data Management System (EDMS) to monitor in-process and finished product quality. This system captures real-time data from electronic measurements during production, ensuring accuracy and compliance with industry standards. The EDMS enhances traceability, enables secure data storage, and streamlines quality control, allowing us to deliver consistently quality packaging solutions.
To ensure compliance and the highest quality standards, our QMS follows FDA 21 CFR Part 11 and ICH Q10 by integrating quality and compliance management processes, complaint handling, document control, change control, audit procedures and training management, and with customer web portal that links corrective actions, nonconforming products, engineering change requests, documents and surveys directly to customers in quality management system.
Inhouse Transportation
Our in-house transportation system enables us to cut down delivery times. We offer flexible shipping options within New Jersey to meet urgent needs swiftly. This capability minimizes inventory costs and streamlines operations, ensuring that our clients receive their products promptly.
Innovation
Regulatory Compliance
With extensive knowledge of pharmaceutical packaging regulations, we ensure that all our products comply with relevant industry standards. This attention to regulatory detail guarantees that your packaging is safe, secure, and compliant, giving you confidence in your choice of supplier. At SURARK Bottles and Closures ensures compliance with FDA regulations by maintaining a Drug Master File (DMF). Our adherence to Current Good Manufacturing Practices (CGMP) ensures that all products meet the highest quality and safety standards.
Raw Materials
All the raw materials used in the manufacture of bottles and closure are procured from qualified suppliers who meet stringent FDA requirements. Our vendor qualification program includes regular audits to ensure ongoing reliability and compliance with established specifications. Each batch is verified for identity, quality, and purity before use.
Quality
Customer Support
We pride ourselves on offering top-notch customer service. Our technical support team is always available to assist with any product-related inquiries. Our approach ensures that customers have direct access to human support for seamless service experience.
Our dedicated team is here to support you throughout the entire process, from product selection to after-sales support. We value strong client relationships and strive to make your experience with us seamless, efficient, and satisfying. Your success is our priority, and we are committed to providing personalized support every step of the way.
Calibrations
All equipment& instrument used in the manufacturing and quality control testing are routinely calibrated according to FDA guidelines to ensure precision and accuracy. Calibration is performed using standards traceable to the National Institute of Standards and Technology (NIST), minimizing measurement uncertainties and ensuring reliable results.