Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.
01 1Shandong Loncom Pharmaceutical Co. Ltd.
02 2M/s Alembic Pharmaceuticals limited
03 1M/s Cipla Ltd
04 1M/s Hetero Labs Ltd
05 1M/s MSN Pharmachem Private Limited
06 1M/s Megafine Pharma P Limited
07 1M/s Morepen laboratories limited
08 1M/s Piramal Pharma Limited
09 1M/s RL Fine Chem Pvt Ltd
10 1M/s Symed Labs Ltd
11 1M/s Unichem Laboratories Limited
12 1M/s. Morepen Laboratories Limited
13 1M/sZydus Lifesciences Limited
Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.
Date of Issue : 2023-06-28
Valid Till : 2026-09-12
Written Confirmation Number : SD230059
Address of the Firm : No. 127, Qizhong Avenue, Qihe County, Dezhou City, Shandong Province, China
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A TRINTELLIX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TRINTELLIX, including repackagers and relabelers. The FDA regulates TRINTELLIX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TRINTELLIX API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A TRINTELLIX supplier is an individual or a company that provides TRINTELLIX active pharmaceutical ingredient (API) or TRINTELLIX finished formulations upon request. The TRINTELLIX suppliers may include TRINTELLIX API manufacturers, exporters, distributors and traders.
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A TRINTELLIX written confirmation (TRINTELLIX WC) is an official document issued by a regulatory agency to a TRINTELLIX manufacturer, verifying that the manufacturing facility of a TRINTELLIX active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting TRINTELLIX APIs or TRINTELLIX finished pharmaceutical products to another nation, regulatory agencies frequently require a TRINTELLIX WC (written confirmation) as part of the regulatory process.
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