Tendocover C2 Plus is a meticulously designed multivitamin formulation integrating bioactive compounds and essential micronutrients to address joint and metabolic health. The product’s composition includes Rose Hip Extract (50mg), Collagen Type II complex (250mg), and Glucosamine Sulphate KCL (750mg), which are combined with Vitamin D3 (1000 IU), Ginger Extract (40mg), and a comprehensive array of vitamins (C, B12, B12), minerals (Iron, Zinc, Manganese, Copper), and trace elements (Folic acid, Selenium). The formulation is engineered to ensure optimal solubility, stability, and bioavailability through advanced excipient selection and controlled-release technology. Each tablet is designed to maintain structural integrity during storage and transit while ensuring uniform active ingredient distribution. The combination of hydrophilic and hydrophobic components is balanced to prevent phase separation, ensuring consistent dosing and product performance. The formulation adheres to pharmaceutical-grade specifications for disintegration time, dissolution rate, and microbial limits, ensuring compliance with regulatory standards for over-the-counter supplements.
Manufacturing Capability
Our manufacturing infrastructure is equipped with state-of-the-art facilities compliant with current Good Manufacturing Practices (cGMP) and ISO 9001 standards. The production process employs advanced tablet compression technology, including high-speed tabletting machines and precision dosing systems, to ensure uniformity in tablet weight, hardness, and content uniformity. Sterile processing capabilities are maintained through dedicated cleanroom environments (Class 10,000–100,000) for critical components, minimizing contamination risks. The facility supports scalable production, enabling seamless transitions from small batch trials to large-scale commercial manufacturing. Quality systems include real-time monitoring of critical process parameters, such as compression force and tablet disintegration, to ensure consistency. Raw material sourcing is rigorously validated, with suppliers meeting ISO 22000 and GMP requirements. The production line is designed for flexibility, accommodating custom formulations and packaging modifications to meet specific client needs.
Available Strengths and Packaging
Tendocover C2 Plus is available in a single dosage strength, formulated to deliver the specified composition per tablet. The product is packaged in 10x1x10 Alu Alu blister packs, ensuring tamper-evident sealing, moisture resistance, and light protection. The packaging design is optimized for stability during transportation and storage, with aluminum foil providing a barrier against environmental contaminants. The blister format supports efficient inventory management and retail display, while the 10x1x10 configuration ensures cost-effective bulk supply for distributors and retailers.
Contract Manufacturing / Third Party Manufacturing
As a trusted pharmaceutical manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to meet the needs of global buyers. Our facility supports private label manufacturing, enabling clients to brand products under their own trademarks while leveraging our expertise in formulation development and regulatory compliance. We provide end-to-end solutions, including raw material sourcing, formulation design, quality control, and packaging, ensuring full traceability and adherence to international standards. Our team collaborates closely with clients to customize production parameters, such as dosage strengths, excipient types, and packaging formats, to align with specific market requirements. Whether for domestic or international markets, we ensure scalable production capabilities, flexible lead times, and compliance with local and global regulatory frameworks.
Quality Assurance
Our quality assurance systems are built on rigorous analytical validation and continuous process monitoring to ensure product consistency and safety. Each batch undergoes comprehensive testing, including high-performance liquid chromatography (HPLC) for active ingredient quantification, microbial limit testing, and dissolution profiling to confirm bioavailability. Raw materials are subjected to incoming inspection, with specifications verified against pharmacopeial standards (e.g., USP, EP, BP). Finished products are tested for physical attributes (e.g., disintegration time, tablet hardness) and chemical purity to meet pharmaceutical-grade requirements. We maintain detailed batch records and employ statistical process control (SPC) to monitor deviations and ensure compliance with cGMP. All quality control procedures are validated to ensure reproducibility, and our laboratory is accredited for ISO 17025 standards, guaranteeing the reliability of analytical results.
Regulatory Compliance
Tendocover C2 Plus is manufactured in full compliance with global regulatory frameworks, including cGMP, WHO guidelines, and ISO 9001/14001 standards. Our facility adheres to the requirements of the U.S. FDA, EU GMP, and ICH guidelines, ensuring products meet the specifications for pharmaceutical quality and safety. We maintain documentation for regulatory submissions, including batch records, stability data, and validation reports, to support compliance with local and international authorities. The product is formulated to meet the pharmacopeial standards for excipients and active ingredients, ensuring compatibility with global market requirements. Our team provides regulatory support, including dossier preparation and compliance audits, to facilitate market entry in diverse regions.
Global Supply Capability
With a robust international distribution network, we ensure reliable bulk supply and export capabilities to over 50 countries. Our logistics partners specialize in temperature-controlled shipping and customs compliance, enabling seamless delivery to remote and challenging markets. The facility is equipped for large-scale production, supporting bulk supply orders ranging from 10,000 to 500,000 tablets per batch, with flexibility to accommodate seasonal demand fluctuations. Our supply chain is designed for resilience, with redundant inventory management systems and contingency planning to mitigate disruptions. We offer customized export solutions, including documentation for FDA, EMA, and local regulatory bodies, ensuring smooth clearance and timely delivery.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners benefit from our expertise in high-quality formulation, regulatory compliance, and scalable production. Our commitment to cGMP and ISO standards ensures product reliability, while our flexible manufacturing capabilities allow customization to meet diverse market needs. We provide end-to-end support, from raw material sourcing to global distribution, reducing time-to-market and operational risks. Our team’s deep knowledge of regulatory frameworks and supply chain logistics enables clients to achieve compliance and competitive advantage in international markets.
Bulk Supply Inquiry
For bulk supply inquiries, please contact our sales team at info@delwishealthcare.com to discuss customization options, pricing, and delivery schedules.
FAQs
Is Tendocover C2 Plus manufactured under cGMP standards?
Yes, all production processes adhere to current Good Manufacturing Practices (cGMP) and ISO 9001 standards.
Can the product be customized for different packaging formats?
Yes, we offer flexible packaging solutions, including blister packs, bottles, and cartons, to meet specific market requirements.
What regulatory approvals are required for exporting Tendocover C2 Plus?
The product complies with FDA, EU GMP, and WHO guidelines, ensuring approval for export to over 50 countries.
How is the stability of Tendocover C2 Plus ensured?
The formulation is tested for stability under accelerated conditions, with a shelf life of 24 months when stored properly.
Can Tendocover C2 Plus be produced in bulk quantities?
Yes, our facility supports bulk production ranging from 10,000 to 500,000 tablets per batch.
What quality control measures are in place for raw materials?
All raw materials undergo rigorous testing for purity, potency, and microbial limits, with supplier audits conducted annually.
How does your company ensure compliance with international regulations?
We maintain full documentation for regulatory submissions and provide support for audits by local authorities.
What is the lead time for bulk orders?
Lead times vary based on order size, but we offer expedited production for urgent requirements.
Can you assist with export documentation and customs clearance?
Yes, our team provides complete documentation, including COA, batch certificates, and export compliance files.
How do you handle supply chain disruptions?
We implement redundant inventory systems and contingency planning to ensure uninterrupted supply, even during global disruptions.
