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IP International Pharmaceuticals production facilities are WHO certified. GMP standards vary from country to country. The United Nations WHO provides stringent requirements for certification of plants to the global standards of the WHO. This certification is known at WHO-GMP and is a mark of quality similar to the USFDA inspection standards.

IP International Pharmaceuticals uses only the highest quality raw material manufactured to United States Pharmacopoeia (USP) or British Pharmacopoeia (BP) standards. From procurement of raw materials to packaging of finished product, our Quality Control (QC) team oversees every step of the manufacturing process.

All products are manufactured according to Good Manufacturing Practices (GMP) facility to ensure optimal quality. Our compliance with ISO 9001 regulations ensures that all aspects of our operations adhere to the highest quality standards.

All products are also analyzed by an independent third-party laboratory for verification of both potency and purity as per GMP and the pharmacopoeia standards.

Related focus includes facilities specializing in:
• BE Studies & eCTD/CIS Dossier Development
• Analytical Laboratories with Biological Support
• Synthetic Organic / Custom API Development
• Medical Device Manufacturing
• Custom Recombinant Work
IP International Pharmaceuticals does not ship to countries, which classify these pharmaceuticals as special controlled or scheduled substances, including but not limited to the United States, Australia, Canada. We are not directly or indirectly associated with any websites that may engage in selling same or similar products. Information contained within this website is not a prescription to use and is intended for information purposes only. We are based in Asia and follow local laws accordingly. All manufacturing is in accordance with USP or BP Guidelines.