Paris Susp is a ready-to-use paracetamol suspension designed for pharmaceutical manufacturers requiring consistent quality and stability. The formulation incorporates paracetamol as the active pharmaceutical ingredient (API), suspended in a stable aqueous base with excipients such as sodium benzoate (preservative), potassium sorbate (antioxidant), and flavoring agents to ensure palatability and shelf-life. The suspension is formulated to maintain a uniform particle dispersion, ensuring consistent API release and ease of dosing. The DPCO (Dose Pack Controlled) designation indicates precise dosing control, critical for pharmaceutical applications requiring accurate delivery. The product’s formulation is optimized for stability under standard storage conditions (15–30°C, 60% RH), with a shelf life of 24 months when stored properly. The suspension’s low viscosity and fine particle dispersion enhance mixing efficiency during manufacturing and ensure homogeneity across batches.
Manufacturing Capability
Our manufacturing infrastructure is designed to meet the stringent demands of pharmaceutical production, with a focus on scalability, sterility, and compliance. The facility is equipped with state-of-the-art equipment, including high-speed mixers, homogenizers, and sterile filtration systems, enabling efficient production of suspensions like Paris Susp. Sterile processing is achieved through ISO 8 cleanroom environments, ensuring contamination-free manufacturing. The facility adheres to current Good Manufacturing Practices (cGMP) and is certified under ISO 9001 for quality management, ensuring consistent product quality. Production scalability is supported by modular manufacturing lines capable of handling bulk orders, with the ability to adjust output based on client requirements. Advanced quality systems, including real-time monitoring and automated data collection, ensure traceability and process control.
Available Strengths and Packaging
Paris Susp is available in a standardized strength of 250mg paracetamol per 5ml of suspension. The product is packaged in a 60ml container, designed for convenient storage and distribution. This packaging format ensures minimal product waste and ease of handling during bulk supply.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing and private label services to pharmaceutical buyers. Our facility is equipped to produce custom formulations under third-party branding, ensuring full compliance with regulatory standards. Clients can leverage our expertise in suspension manufacturing to develop products tailored to specific market needs, including variations in strength, packaging, and labeling. Our team provides end-to-end support, from formulation development to packaging and quality assurance, enabling seamless integration into global supply chains.
Quality Assurance
Quality assurance is a cornerstone of our manufacturing process, with rigorous testing protocols ensuring compliance with international standards. Each batch undergoes comprehensive analytical validation, including testing for API potency, impurity profiling, and dissolution rate. Advanced spectroscopic and chromatographic techniques are employed to verify consistency and purity. Microbial limit testing, pH measurement, and particulate matter analysis are conducted to ensure product safety and stability. Our quality control systems are aligned with USP, EP, and BP guidelines, with documented batch records and traceability protocols to support regulatory audits.
Regulatory Compliance
Our manufacturing processes are fully compliant with global regulatory frameworks, including cGMP, WHO guidelines, and ISO 9001/14001 standards. The facility is registered with major regulatory authorities, such as the FDA, EMA, and MHRA, ensuring adherence to quality and safety benchmarks. Products are manufactured in accordance with WHO’s Prequalification Programme (PQP) requirements, making them suitable for export to developing markets. Environmental management systems are in place to meet ISO 14001 standards, reflecting our commitment to sustainable manufacturing practices.
Global Supply Capability
We provide reliable bulk supply capabilities to meet the demands of international markets. Our export-ready products are distributed through a well-established global network, with logistics partners covering key regions including Asia, Africa, Latin America, and Europe. The 60ml packaging format is ideal for bulk supply, with scalable options to accommodate large orders. Our supply chain is designed for resilience, featuring redundant storage facilities and real-time tracking systems to ensure timely delivery. We maintain inventory for critical components to minimize production downtime and guarantee uninterrupted supply.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our combination of expertise, compliance, and scalability. Our cGMP-certified facility ensures high-quality output, while our flexible manufacturing capabilities allow customization to meet diverse market needs. As a trusted supplier, we offer competitive pricing, rapid turnaround times, and dedicated support to streamline procurement processes. Our commitment to regulatory compliance and sustainability positions us as a reliable partner for global pharmaceutical operations.
Bulk Supply Inquiry
We offer robust bulk supply capabilities to meet the demands of large-scale pharmaceutical operations. For inquiries regarding bulk orders, please contact our sales team at info@delwishealthcare.com.
FAQs
What manufacturing standards does Paris Susp comply with?
Paris Susp is manufactured in accordance with cGMP, WHO guidelines, and ISO 9001 standards, ensuring compliance with global regulatory requirements.
Can Paris Susp be produced in different packaging formats?
While the standard packaging is 60ml, we offer customization options for bulk supply, including alternative container sizes and labeling requirements.
What is the shelf life of Paris Susp?
Paris Susp has a shelf life of 24 months when stored under recommended conditions (15–30°C, 60% RH).
Does the product require special storage conditions?
No, Paris Susp is stable under standard storage conditions and does not require refrigeration.
Can your facility produce private-label versions of Paris Susp?
Yes, we offer private-label manufacturing services, allowing clients to brand the product under their own name.
What quality control measures are in place for batch testing?
Each batch undergoes rigorous testing for API potency, microbial limits, pH, and dissolution rate, ensuring compliance with USP, EP, and BP standards.
Are your products suitable for export to developing markets?
Yes, our products meet WHO PQP requirements, making them ideal for export to regions with stringent quality standards.
How do you ensure supply chain reliability?
Our supply chain is supported by redundant storage facilities, real-time tracking systems, and partnerships with global logistics providers to ensure timely delivery.
Can you accommodate custom formulation requests?
Yes, we provide formulation development services to tailor products to specific market needs, including variations in strength and excipient composition.
What is the minimum order quantity for bulk supply?
Minimum order quantities are flexible and can be customized based on client requirements, with options for small to large-scale production.
