Vitend C2 fort is a precision-formulated tablet designed for pharmaceutical manufacturers seeking high-quality, stable, and bioavailable active ingredients. The formulation integrates Undenatured Collagen Type II (40mg), Boswellia Serrata Extract (100mg), Curcumin (100mg), Sodium Hyaluronate (50mg), and Rosehip Extract (500mg) into a cohesive matrix optimized for uniformity, disintegration, and dissolution. The excipients and binding agents are selected to ensure compatibility with the active compounds, maintaining chemical stability during storage and processing. The tablet’s formulation adheres to pharmaceutical-grade standards, with controlled particle size, moisture content, and compression force to ensure consistent dosing. The manufacturing process employs advanced tableting technology to achieve high-density, uniform tablets with minimal friability, ensuring product integrity during handling and distribution.
Manufacturing Capability
Our manufacturing infrastructure is equipped with state-of-the-art facilities designed to meet stringent pharmaceutical standards. The facility includes a dedicated tablet compression line, high-speed tablet machines, and a controlled environment for blending and granulation. Sterile processing capabilities are available for sensitive ingredients, ensuring contamination-free production. All manufacturing processes comply with current Good Manufacturing Practices (cGMP), with continuous monitoring of critical parameters such as temperature, humidity, and particle size. The production line is scalable to accommodate bulk supply requirements, with the ability to produce large quantities while maintaining consistency in quality and potency. Quality systems are integrated throughout the manufacturing process, including in-process testing, final product inspection, and documentation of all production parameters to ensure compliance with regulatory requirements.
Available Strengths and Packaging
Vitend C2 fort is available in a single strength formulation, with each tablet containing 40mg of Undenatured Collagen Type II, 100mg of Boswellia Serrata Extract, 100mg of Curcumin, 50mg of Sodium Hyaluronate, and 500mg of Rosehip Extract. The product is packaged in 10x1x10 Alu Alu blister packs, ensuring protection against moisture, light, and physical damage. The blister pack design facilitates easy handling, storage, and distribution, making it ideal for pharmaceutical buyers requiring reliable packaging solutions.
Contract Manufacturing / Third Party Manufacturing
As a trusted manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to pharmaceutical buyers’ needs. Our capabilities include private label manufacturing, where we produce finished products under a client’s brand name, and contract manufacturing for raw material-based formulations. We support customization of dosage forms, excipients, and packaging to meet specific regulatory and market requirements. Our team collaborates closely with clients to ensure alignment with quality standards, production timelines, and cost-efficiency. Whether sourcing bulk raw materials or requiring end-to-end manufacturing, we provide flexible solutions that prioritize compliance, scalability, and innovation.
Quality Assurance
Our quality assurance framework is built on rigorous analytical validation, batch testing, and adherence to pharmaceutical quality standards. Each production batch undergoes in-process testing for critical parameters such as weight variation, disintegration time, and dissolution rate. Finished products are subjected to final quality control checks, including HPLC analysis for active ingredient quantification and microbial testing to ensure safety. We maintain detailed documentation of all quality control measures, ensuring traceability and compliance with international standards. Our quality systems are validated to meet USP, EP, and BP requirements, with regular audits and calibration of analytical instruments to maintain precision and accuracy.
Regulatory Compliance
Vitend C2 fort is manufactured in full compliance with Good Manufacturing Practices (GMP), World Health Organization (WHO) guidelines, and international ISO standards. Our facility is certified under ISO 9001 for quality management and ISO 14001 for environmental management, ensuring sustainable and compliant production. We adhere to regulatory frameworks such as the FDA’s Current Good Manufacturing Practice (CGMP) and the European Medicines Agency (EMA) guidelines, enabling seamless export to global markets. All documentation, including batch records, stability data, and certificates of analysis, is prepared to meet the requirements of regulatory authorities worldwide.
Global Supply Capability
We provide reliable global supply capabilities, with a well-established international distribution network and bulk supply capacity to meet large-scale demand. Our export logistics are supported by partnerships with trusted freight forwarders and customs brokers, ensuring timely delivery to destinations across Asia, Europe, Africa, and the Americas. The 10x1x10 Alu Alu packaging is designed for efficient storage and transportation, reducing the risk of damage during transit. Our supply chain is optimized for consistency, with inventory management systems in place to ensure uninterrupted delivery. We prioritize supply chain reliability through strategic sourcing, contingency planning, and real-time tracking of shipments.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners select us for our expertise in high-quality formulation, regulatory compliance, and scalable production. Our commitment to cGMP standards, advanced manufacturing technology, and global regulatory alignment ensures that Vitend C2 fort meets the demands of diverse markets. We offer competitive pricing, timely delivery, and dedicated support to enhance client satisfaction. With a focus on innovation and sustainability, we provide end-to-end solutions that align with the evolving needs of the pharmaceutical industry.
Bulk Supply Inquiry
For bulk supply inquiries, please contact us at info@delwishealthcare.com. Our team is ready to assist with customized solutions, including large-scale production, packaging requirements, and export logistics.
FAQs
What is the shelf life of Vitend C2 fort?
The product has a shelf life of 24 months when stored in its original packaging under controlled conditions.
Can Vitend C2 fort be customized for different dosage forms?
Yes, we offer customization options for dosage forms, including tablets, capsules, and soft gel capsules, based on client specifications.
Does the manufacturing process ensure sterility for sensitive ingredients?
Yes, our facility includes sterile processing capabilities to ensure contamination-free production of sensitive ingredients.
What certifications does your facility hold?
Our facility is certified under ISO 9001, ISO 14001, and complies with GMP, WHO, and FDA regulations.
Can you provide documentation for regulatory approvals?
Yes, we supply complete documentation, including batch records, stability data, and certificates of analysis, to meet global regulatory requirements.
What is the minimum order quantity for bulk supply?
Minimum order quantities are flexible and can be customized based on production capacity and client requirements.
How do you ensure the bioavailability of the active ingredients?
The formulation is optimized for enhanced bioavailability through advanced excipient selection, controlled release technology, and rigorous stability testing.
Can you support private label manufacturing?
Yes, we provide private label manufacturing services, allowing clients to brand the product under their own name.
What is the packaging material’s compliance status?
The 10x1x10 Alu Alu packaging is compliant with pharmaceutical standards for moisture, light, and physical protection.
How do you handle supply chain disruptions?
We implement contingency planning, including diversified supplier networks and inventory management systems, to ensure uninterrupted supply.
