Top Pharmaceutical Company in India | Tanishq Lifecare

Tanishq Lifecare has earned its reputation as one of the foremost OTC drug export companies in India through a combination of rigorous quality standards and proven export capabilities. Our manufacturing facilities are WHO-GMP certified, ensuring compliance with international quality benchmarks. We have a strong regulatory team that navigates complex export requirements seamlessly, enabling us to export to over 75 countries worldwide. Our commitment to maintaining transparency, consistency, and timely delivery further cements our position as a reliable partner for global OTC pharmaceutical needs.

We have invested heavily in cutting-edge manufacturing technology, including fully automated production lines and advanced quality control systems. Our quality assurance team implements stringent protocols to ensure that every batch meets international pharmacopeia standards. We prioritize innovation through continuous R&D, developing new formulations and improving existing ones to stay ahead in the dynamic OTC market. Additionally, our flexible manufacturing capabilities allow us to handle diverse product portfolios—from tablets and capsules to liquids and topical formulations—making us a preferred choice for many clients.

Our export footprint spans multiple continents, reflecting our global reach and expertise in international trade compliance. In Africa, we serve markets like Nigeria, Kenya, South Africa, and Tanzania. The Middle East includes the UAE, Saudi Arabia, Oman, and Qatar, while in the Commonwealth of Independent States (CIS) region, we cater to Russia, Kazakhstan, and Uzbekistan. We also export to Latin American countries such as Brazil, Mexico, and Colombia, and have a growing presence in Southeast Asia, including Vietnam, the Philippines, and Indonesia. Our broad geographical reach is supported by localized market knowledge and compliance with regional regulatory requirements.

Navigating export documentation can be complex, but our experienced export team provides comprehensive support to simplify the process. We prepare all essential documentation including Certificates of Analysis, which validate the quality and composition of the products, GMP Certificates that demonstrate compliance with manufacturing standards, and Free Sale Certificates to confirm product eligibility for sale in the importing country. We also develop detailed product dossiers tailored to the regulatory requirements of the destination country and ensure shipment-specific documentation such as customs declarations, packing lists, and bills of lading are complete and accurate to prevent any delays.

Absolutely. We offer end-to-end third-party manufacturing solutions for OTC drugs that encompass everything from initial formula optimization to final packaging and bulk production. Our expert formulation team works closely with clients to optimize product efficacy and stability. We ensure full regulatory compliance across markets, assist with packaging design that aligns with brand identity, and deliver large-scale manufacturing capabilities with consistent quality. This makes us a preferred contract manufacturing partner for both emerging and established pharmaceutical brands looking to expand their product lines.

Quality is at the core of our operations, reflected by multiple internationally recognized certifications. Our WHO-GMP certification affirms our adherence to global pharmaceutical manufacturing standards. We are also ISO 13485:2016 certified, underscoring our compliance with medical device quality management systems. Additionally, we maintain country-specific certifications as required by various regulatory agencies and undergo regular audits by authorities such as the US FDA and European Medicines Agency (EMA). These certifications not only validate our quality systems but also enhance our customers' confidence in our products.

Our manufacturing infrastructure is designed for high-volume, efficient production. We currently have the capacity to produce up to 5 million tablets per day, 2 million capsules per day, and approximately 50,000 liters of liquid formulations each month. This scale allows us to cater to large orders from global clients while maintaining product quality and meeting delivery deadlines. Our facilities are scalable, enabling us to ramp up production as per client demands or new contract requirements.

Handling temperature-sensitive products requires specialized logistics and packaging to maintain product integrity. We have climate-controlled warehouses that store temperature-sensitive items under optimal conditions. For shipments, we employ temperature-monitored transport solutions and utilize cold chain packaging materials designed to maintain consistent temperatures throughout transit. Our robust cold chain management system minimizes the risk of degradation due to heat or humidity, ensuring that sensitive OTC drugs reach customers in perfect condition regardless of destination.