Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
01 1M/s. Synthokem Labs Pvt, Ltd.,
01 1IMCD Korea Co., Ltd.
01 1Chlorphenesin carbamate
01 1India
Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
Registrant Name : IMCD Korea Co., Ltd.
Registration Date : 2022-01-10
Registration Number : 20220110-209-J-1134
Manufacturer Name : M/s. Synthokem Labs Pvt, Ltd...
Manufacturer Address : Unit-II, Plot No. 222 to 224 & 235 to 237, Phase-II, IDA, Pashamylaram, Patancheru Ma...
A Chlorphenesin Carbamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorphenesin Carbamate, including repackagers and relabelers. The FDA regulates Chlorphenesin Carbamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorphenesin Carbamate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Chlorphenesin Carbamate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorphenesin Carbamate supplier is an individual or a company that provides Chlorphenesin Carbamate active pharmaceutical ingredient (API) or Chlorphenesin Carbamate finished formulations upon request. The Chlorphenesin Carbamate suppliers may include Chlorphenesin Carbamate API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorphenesin Carbamate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Chlorphenesin Carbamate Drug Master File in Korea (Chlorphenesin Carbamate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Chlorphenesin Carbamate. The MFDS reviews the Chlorphenesin Carbamate KDMF as part of the drug registration process and uses the information provided in the Chlorphenesin Carbamate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Chlorphenesin Carbamate 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 Chlorphenesin Carbamate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Chlorphenesin Carbamate suppliers with KDMF on PharmaCompass.
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