Diamine Fort is a precision-formulated pharmaceutical tablet combining three active ingredients: Diacerein (50mg), Glucosamine Sulphate Potassium Chloride (750mg), and Methyl Sulfonyl Methane (250mg). The formulation is designed to ensure optimal bioavailability, stability, and uniformity through advanced excipient selection and controlled manufacturing processes. Diacerein, a synthetic compound, is incorporated to modulate inflammatory responses, while Glucosamine Sulphate Potassium Chloride provides chondroprotective benefits. Methyl Sulfonyl Methane (MSM) is included for its anti-inflammatory and antioxidant properties. The tablet is manufactured using direct compression techniques, ensuring consistent disintegration and dissolution profiles. The formulation is stabilized through controlled pH buffering and moisture-resistant excipients, maintaining product integrity under varied storage conditions. The combination of these components is engineered to meet stringent pharmaceutical specifications for potency, purity, and uniformity.
Manufacturing Capability
Our manufacturing infrastructure is equipped with state-of-the-art facilities compliant with current Good Manufacturing Practices (cGMP) and ISO 9001:2015 standards. The facility includes advanced tablet compression machines, high-precision blending systems, and automated packaging lines capable of handling complex formulations like Diamine Fort. Sterile processing capabilities are available for critical components, ensuring contamination-free production. The facility adheres to strict quality control protocols, including real-time monitoring of critical parameters such as particle size, moisture content, and tablet hardness. Production scalability is achieved through modular manufacturing units, enabling seamless transitions from small-scale trials to large-volume commercial batches. Comprehensive quality systems, including validation of equipment and processes, ensure consistent product quality and regulatory compliance.
Available Strengths and Packaging
Diamine Fort is available in a single strength: Diacerein 50mg + Glucosamine Sulphate Potassium Chloride 750mg + Methyl Sulfonyl Methane 250mg. The product is packaged in 10x10 Alu Alu blister packs, ensuring tamper-evident sealing, moisture resistance, and compliance with pharmaceutical packaging standards. The aluminum-aluminum blister format provides optimal protection against light, humidity, and physical damage, ensuring product stability during storage and transportation.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer end-to-end contract manufacturing, private label production, and third-party manufacturing services tailored to pharmaceutical buyers. Our capabilities include formulation development, API integration, and finished dosage form production, with flexibility to meet specific regulatory and quality requirements. We support private label manufacturing for branded products, ensuring full customization of packaging, labeling, and compliance documentation. Third-party manufacturing services are available for global clients, with dedicated project management teams to oversee production timelines, quality assurance, and regulatory submissions. Our scalable infrastructure ensures adherence to international standards while maintaining cost-efficiency and supply chain reliability.
Quality Assurance
Our quality assurance framework is built on rigorous analytical validation, batch testing, and adherence to pharmaceutical quality standards. Each batch of Diamine Fort undergoes comprehensive testing, including high-performance liquid chromatography (HPLC) for active ingredient quantification, dissolution testing to ensure bioavailability, and microbial limit testing for contamination control. In-process quality checks are performed at critical stages of manufacturing, such as blending, compression, and packaging. Analytical validation protocols ensure method accuracy, precision, and reproducibility, while documentation compliance meets FDA, EMA, and WHO requirements. Continuous improvement initiatives and root-cause analysis frameworks ensure timely resolution of quality deviations.
Regulatory Compliance
Diamine Fort is manufactured in full compliance with Good Manufacturing Practices (GMP), World Health Organization (WHO) guidelines, and ISO 9001:2015 quality management standards. Our facility is registered with global regulatory authorities, including the FDA, EMA, and MHRA, ensuring alignment with international pharmacopeia requirements. Compliance with ISO 17025 standards for laboratory accreditation guarantees the reliability of analytical testing. We maintain detailed documentation for regulatory submissions, including batch records, stability data, and deviation reports. Our commitment to regulatory compliance ensures seamless market access in over 50 countries, with adherence to local import/export regulations and labeling requirements.
Global Supply Capability
Our global supply chain is designed to meet the demands of international pharmaceutical markets, with robust export capabilities and a comprehensive distribution network. We provide bulk supply options for large-scale distributors and exporters, ensuring consistent delivery timelines and competitive pricing. Our logistics partners facilitate seamless cross-border shipments, with compliance to international shipping regulations and pharma-specific handling protocols. Bulk supply capacity is supported by scalable production lines and inventory management systems, ensuring supply chain reliability even during peak demand. We prioritize sustainability in logistics, employing eco-friendly packaging and carbon-neutral shipping options to meet global environmental standards.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners select us for our unwavering commitment to quality, regulatory compliance, and operational excellence. Our expertise in complex formulation development and scalable manufacturing ensures timely delivery of high-standard products. We offer end-to-end solutions, from raw material sourcing to finished product packaging, with full transparency in production processes. Our global regulatory expertise and localized compliance support enable seamless market entry, while our dedicated customer service team ensures tailored solutions for diverse client needs. Partnering with us guarantees access to a reliable, compliant, and innovative pharmaceutical supply chain.
Bulk Supply Inquiry
We offer competitive bulk supply options for Diamine Fort. For inquiries regarding large-scale procurement, please contact our sales team at info@delwishealthcare.com.
FAQs
What manufacturing standards does Diamine Fort comply with?
Diamine Fort is manufactured in compliance with cGMP, WHO guidelines, ISO 9001:2015, and regional regulatory frameworks, ensuring global market access.
Can Diamine Fort be customized for private label manufacturing?
Yes, we offer private label manufacturing services, allowing full customization of packaging, labeling, and regulatory documentation.
What is the shelf life of Diamine Fort?
The product has a shelf life of 24 months when stored under recommended conditions (cool, dry, and protected from light).
Does Diamine Fort require special storage conditions?
No, Diamine Fort is stable under standard pharmaceutical storage conditions and does not require refrigeration.
What certifications does your facility hold?
Our facility is certified under ISO 9001:2015, GMP, and ISO 17025 for analytical testing, ensuring compliance with international standards.
Can you supply Diamine Fort in bulk for export?
Yes, we provide bulk supply options for global exporters, with scalable production capacity and logistics support for international shipments.
How do you ensure product consistency during large-scale manufacturing?
We use advanced quality control systems, including real-time monitoring and batch testing, to ensure consistency across all production runs.
What is the minimum order quantity for Diamine Fort?
Minimum order quantities are flexible and can be tailored to meet the specific needs of pharmaceutical buyers.
Can you accommodate regulatory submissions for different markets?
Yes, our team supports regulatory submissions for global markets, including FDA, EMA, and local regulatory authorities.
How do you handle supply chain disruptions?
We maintain a diversified supply chain and inventory management system to ensure uninterrupted supply, even during unforeseen disruptions.
