Holds one valid CEP for crospovidone, filing since 2015. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one valid CEP for crospovidone, filing since 2023.
Holds one valid CEP for crospovidone, filing since 2023.
Holds one valid CEP for crospovidone, filing since 2021.
Holds one valid CEP for crospovidone, filing since 2021.
Holds one valid CEP for crospovidone, filing since 2019.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
Contract manufacturers make to order rather than holding their own filing for this molecule.
The order is set by active filings weighted by regulator, inspection outcomes and their recency, breadth of GMP recognition, and evidence of real exports, less any open risk flags. Every factor appears on the card it produced. Read the full method.
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