Network
Our network comprises a carefully selected group of pharmaceutical manufacturing plants that hold all required regulatory approvals—such as WHO-GMP, EU-GMP, USFDA, MHRA, and other international certifications—ensuring global compliance and quality standards. Each facility within our network is equipped with the technical expertise and infrastructure to support diverse dosage forms, including tablets, capsules, injectables, ointments, and nutraceuticals. Additionally, we maintain a comprehensive library of product dossiers (CTD/ACTD formats) to facilitate smooth registration and market entry in various countries. This integrated network enables us to efficiently cater to both private market supply and government tenders, offering our partners reliable, compliant, and ready-to-register pharmaceutical solutions.
Large capacity
Our large-capacity manufacturing network is strategically designed to meet high-volume pharmaceutical export demands while maintaining shorter delivery timelines. With multiple production facilities operating across key therapeutic segments, we have the flexibility and scale to handle bulk orders for both finished formulations and raw materials. Advanced manufacturing lines, automated packaging units, and robust supply chain management systems enable us to ensure consistent output without compromising on quality or compliance. This extensive capacity allows us to support our global partners—whether for tender supplies, institutional procurement, or private market distribution—with reliable, timely, and cost-effective pharmaceutical products.
Cost effective
We offer cost-effective pharmaceutical solutions by optimizing our sourcing, manufacturing, and logistics processes to deliver the best value per dose without compromising on quality or compliance. Our strong partnerships with accredited manufacturers and suppliers enable us to achieve economies of scale, ensuring competitive pricing for global markets. Moreover, we provide customization as per client specifications, including formulation strength, packaging design, labeling, and regulatory documentation, to meet diverse market and registration requirements. This combination of affordability, flexibility, and compliance makes us a preferred partner for pharma exports across both private and institutional sectors.
Latest technology
As a globally focused pharma export company, we ensure quick adaptation to the latest technologies in pharmaceutical manufacturing and quality assurance. Our international exposure allows us to stay aligned with evolving global standards, regulatory updates, and technological advancements across the industry. By collaborating with manufacturing partners equipped with state-of-the-art facilities, automated systems, and advanced analytical tools, we enhance product quality, efficiency, and consistency. This proactive approach enables us to deliver world-class pharmaceutical products that meet the expectations of our partners across diverse international markets.
CGMP Level Plants
Our network comprises CGMP (Current Good Manufacturing Practice)–compliant manufacturing plants, ensuring that all production facilities meet the highest international quality and safety standards as mandated by global regulatory authorities. While selecting our network partners, we prioritize plants that possess the necessary regulatory approvals such as USFDA, EU-GMP, MHRA, TGA, WHO-GMP, and other country-specific certifications.
Each selected facility maintains a comprehensive set of product dossiers (CTD/ACTD formats), enabling swift regulatory submissions and product registrations across global markets. This robust network allows us to efficiently cater to pharmaceutical exports by offering products that are already approved or dossier-ready, reducing lead time for market entry and ensuring seamless compliance with destination country regulations.
In essence, our approach guarantees that every product sourced or manufactured within our network adheres to stringent international regulatory requirements, ensuring quality, safety, and global acceptability.
Due Diligence
As a responsible pharmaceutical exporter, we conduct comprehensive due diligence before finalizing any business partnership or supply agreement. Our senior management team personally oversees this process to ensure that every collaboration meets the highest standards of regulatory compliance, financial integrity, and ethical business practices.
This includes thorough verification of the partner’s manufacturing licenses, GMP certifications, regulatory approvals, quality systems, and product dossiers, as well as an evaluation of their market reputation and operational capabilities. Financial and legal checks are also performed to confirm reliability and long-term sustainability.
By performing such detailed due diligence, we ensure that all our partnerships are transparent, compliant, and aligned with global pharmaceutical standards, thereby safeguarding product quality and maintaining our commitment to trust, safety, and excellence in international trade.
Future Expansion
Cost-Effective Supply per Dose and Customization as per Client Specifications
As part of our future expansion strategy, we aim to strengthen our manufacturing and sourcing capabilities to ensure a cost-effective supply per dose without compromising on quality. By optimizing production processes, leveraging economies of scale, and maintaining strategic partnerships with efficient CGMP-certified plants, we are able to offer competitive pricing that meets the cost expectations of global clients and government tenders.
In addition, we emphasize customization as per client specifications, offering flexibility in formulations, packaging, labeling, and regulatory documentation to suit the specific requirements of each market. Whether it’s adapting to local regulatory needs, pack sizes, or branding guidelines, our team ensures that every product delivered is tailor-made to fit the client’s market and distribution model.
This dual focus on cost efficiency and customization positions us as a trusted global pharma exporter capable of delivering high-quality, affordable, and market-ready healthcare solutions to our international partners.
Regulatory
Comprehensive Technical, Regulatory & Commercial Support with Compliance and Quality
At SEVDA Pharma, we offer end-to-end technical, regulatory, and commercial support to our global partners, ensuring that every product meets the highest standards of compliance and quality. Our dedicated regulatory team assists clients with dossier preparation (CTD/ACTD formats), product registration, variation filings, and renewals in accordance with the specific requirements of each country.
We also provide complete technical documentation, including product specifications, stability data, GMP certifications, and analytical method validations to support smooth regulatory submissions. On the commercial side, we ensure transparent communication, competitive pricing, and efficient logistics coordination, enabling timely delivery and seamless market entry.
By combining regulatory expertise with strict adherence to international quality norms, SEVDA Pharma ensures that all our products and operations align with the global regulatory landscape, reinforcing our commitment to excellence, compliance, and customer satisfaction.
❮
❯
