Thank you for writing to us. One of our executive will reach back to you through your submitted medium. In case there’s an urgency, feel free to connect over WhatsApp for faster response.
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Yes, in most countries. We recommend appointing a licensed local technical representative or distributor who can submit the dossier, handle communications with the NMRA, and manage post-registration pharmacovigilance. We provide full support and Power of Attorney documents.
We are a WHO-GMP certified manufacturer committed to supplying high-quality, affordable generic medicines. Our products meet international standards (including those recognized by African NMRAs) and we provide full regulatory support, including CTD dossiers, CoPP, and stability data tailored to African climatic zones (Zone IV). We focus on essential medicines, anti-infectives, chronic disease treatments, and more
Yes. All our manufacturing facilities hold valid WHO-GMP certification. We provide complete documentation packages including: Certificate of Pharmaceutical Product (CoPP) Certificate of Analysis (CoA) Free Sale Certificate Stability studies (real-time and accelerated) Bioequivalence data where required
We have NUmber of Suppliemnt good quality Product for Africa market more than 20 Countries we are Exporting our product and after VItabiotics we are the Leading market
Price competitively while factoring in registration costs, duties, and logistics. also we have UAE office there we can accept the CAsh Payment againts Invoice
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