EVita Plus is formulated as a softgel capsule containing a synergistic blend of Vitamin E (400IU), Wheat Germ Oil (100mg), and Omega 3 Fatty Acid (30mg). The formulation leverages advanced excipient compatibility and emulsification techniques to ensure uniform dispersion of lipid-based ingredients within the gelatin matrix. Vitamin E, a fat-soluble antioxidant, is incorporated to enhance oxidative stability, while Wheat Germ Oil provides additional tocopherol content and contributes to the lipid matrix. Omega 3 Fatty Acid is encapsulated to maintain bioavailability and prevent degradation during storage. The softgel design ensures controlled release, protects sensitive ingredients from environmental exposure, and facilitates easy oral administration. The formulation adheres to pharmaceutical-grade standards for purity, homogeneity, and shelf-life stability, making it suitable for integration into bulk pharmaceutical supply chains.
Manufacturing Capability
EVita Plus is manufactured using state-of-the-art pharmaceutical infrastructure compliant with current Good Manufacturing Practices (cGMP). The production process employs sterile processing capabilities, including ISO Class 7 cleanroom environments, to ensure contamination-free handling of lipid-based ingredients. Advanced encapsulation technology is utilized to achieve consistent capsule filling, sealing, and coating, with precise control over fill weight and dimensional tolerances. The facility is equipped for large-scale production, with scalable manufacturing lines capable of handling bulk orders while maintaining quality consistency. Automated quality control systems, including in-process monitoring and real-time data analytics, ensure adherence to pharmacopeial standards. The manufacturing process also incorporates energy-efficient systems and waste-minimization protocols to align with sustainable pharmaceutical practices.
Available Strengths and Packaging
EVita Plus is available in a single strength formulation: Vitamin E 400IU + Wheat Germ Oil 100mg + Omega 3 Fatty Acid 30mg in softgel capsules. The product is packaged in 10x1x10Blister format, which provides optimal protection against moisture, light, and physical damage. The blister packaging ensures tamper-evidence, easy dispensing, and extended shelf-life, making it ideal for distribution in both domestic and international markets.
Contract Manufacturing / Third Party Manufacturing
As a leading pharmaceutical manufacturer, we offer comprehensive contract manufacturing and third-party production services tailored to meet the needs of global buyers. Our private label manufacturing capabilities enable clients to produce branded formulations under their own specifications, with full traceability and regulatory documentation. We support customization of dosage forms, excipient blends, and packaging formats, ensuring alignment with regional regulatory requirements. Our contract manufacturing division adheres to cGMP, ISO 9001, and WHO guidelines, providing end-to-end solutions for pharmaceutical suppliers, exporters, and distributors seeking reliable, scalable production.
Quality Assurance
EVita Plus undergoes rigorous quality control systems to ensure compliance with international pharmaceutical standards. Each batch is subjected to in-process testing for homogeneity, fill weight accuracy, and microbial contamination. Analytical validation is performed using High-Performance Liquid Chromatography (HPLC) and UV spectrophotometry to confirm active ingredient potency and purity. Finished products are tested for dissolution rates, disintegration time, and physical integrity to guarantee consistent performance. All quality control measures are documented in accordance with ICH and USP guidelines, ensuring transparency and traceability for regulatory submissions and supply chain audits.
Regulatory Compliance
EVita Plus is manufactured in full compliance with Good Manufacturing Practices (GMP), WHO guidelines, and ISO 9001:2015 standards. The product meets pharmacopeial requirements for active pharmaceutical ingredients (APIs) and excipients, with documentation supporting compliance with FDA, EMA, and PIC/S regulations. Our facility is certified under ISO 14001 for environmental management and ISO 22000 for food safety, reflecting a commitment to global regulatory excellence. All production processes, including raw material sourcing, formulation, and packaging, are validated to ensure adherence to international quality frameworks.
Global Supply Capability
Our global supply chain is designed to meet the demands of pharmaceutical exporters and distributors worldwide. With a robust international distribution network, we facilitate seamless export to over 50 countries, supported by logistics partners specializing in pharmaceutical freight. Bulk supply capacity is optimized through automated packaging lines and inventory management systems, ensuring timely delivery of orders. Supply chain reliability is maintained through real-time tracking, contingency planning, and compliance with customs regulations. Our ability to scale production and adapt to regional market needs makes us a trusted partner for bulk pharmaceutical supply.
Why Choose Us
Pharmaceutical distributors, exporters, and contract manufacturing partners select EVita Plus for its combination of technical excellence, regulatory compliance, and operational scalability. Our manufacturer’s expertise in lipid-based formulations ensures high-quality, stable products suitable for global markets. With a proven track record of meeting stringent quality and regulatory standards, we provide reliable bulk supply solutions that reduce time-to-market and minimize compliance risks. Our commitment to innovation, sustainability, and customer-centric service positions us as a strategic partner for businesses seeking to expand their pharmaceutical portfolio.
Bulk Supply Inquiry
For bulk supply inquiries, contact our sales team at info@delwishealthcare.com to discuss customization options, pricing, and logistics.
FAQs
What manufacturing standards does EVita Plus adhere to?
EVita Plus is manufactured in compliance with cGMP, ISO 9001, and WHO guidelines, ensuring adherence to international pharmaceutical quality standards.
Can EVita Plus be produced in different packaging formats?
While the standard packaging is 10x1x10Blister, we offer customization for alternative packaging formats upon request, subject to regulatory approval.
What is the shelf life of EVita Plus?
The product has a shelf life of 24 months when stored in controlled conditions (15–25°C, 45%–65% RH), with stability confirmed through accelerated testing.
Does EVita Plus require special storage conditions?
No, EVita Plus is stable under normal storage conditions. However, it should be protected from excessive heat and light to maintain potency.
Can EVita Plus be produced in bulk for export?
Yes, our facility is equipped for large-scale production, with bulk supply capabilities to meet international demand.
What quality control tests are performed on EVita Plus?
Each batch undergoes testing for homogeneity, microbial load, dissolution rate, and HPLC analysis to ensure potency and purity.
Is EVita Plus compliant with FDA and EMA regulations?
Yes, the product meets all regulatory requirements for export to the US, EU, and other global markets.
How does your company ensure supply chain reliability?
We maintain a robust logistics network, real-time tracking systems, and contingency plans to ensure timely and reliable delivery of bulk orders.
Can EVita Plus be customized for private label manufacturing?
Yes, our contract manufacturing services allow for private label production, with full documentation and regulatory support.
What certifications does your facility hold?
Our facility is certified under ISO 9001, ISO 14001, and ISO 22000, reflecting our commitment to quality, environmental management, and food safety standards.
