Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG
01 1Hiple Co., Ltd.
01 1Gonadorelin acetate
01 1Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registrant Name : Hiple Co., Ltd.
Registration Date : 2022-02-15
Registration Number : 20220215-210-J-1148
Manufacturer Name : Bachem AG
Manufacturer Address : Hauptstrasse 144, 4416 Bubendorf, Switzerland
95
PharmaCompass offers a list of Gonadorelin Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Gonadorelin Acetate manufacturer or Gonadorelin Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Gonadorelin Acetate API Price utilized in the formulation of products. Gonadorelin Acetate API Price is not always fixed or binding as the Gonadorelin Acetate Price is obtained through a variety of data sources. The Gonadorelin Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gonadorelin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gonadorelin Acetate, including repackagers and relabelers. The FDA regulates Gonadorelin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gonadorelin Acetate 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 Gonadorelin Acetate supplier is an individual or a company that provides Gonadorelin Acetate active pharmaceutical ingredient (API) or Gonadorelin Acetate finished formulations upon request. The Gonadorelin Acetate suppliers may include Gonadorelin Acetate API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Gonadorelin Acetate Drug Master File in Korea (Gonadorelin Acetate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Gonadorelin Acetate. The MFDS reviews the Gonadorelin Acetate KDMF as part of the drug registration process and uses the information provided in the Gonadorelin Acetate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Gonadorelin Acetate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Gonadorelin Acetate API can apply through the Korea Drug Master File (KDMF).
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