01 1Cambridge Isotope Laboratories, Inc.
01 1urea(13C)
01 1U.S.A
Registration Number : 221MF10045
Registrant's Address : 3 Highwood Drive, Tewksbury, MA 01876, USA
Initial Date of Registration : 2009-02-25
Latest Date of Registration : 2018-11-16
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PharmaCompass offers a list of Urea C13 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 Urea C13 manufacturer or Urea C13 supplier for your needs.
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PharmaCompass also assists you with knowing the Urea C13 API Price utilized in the formulation of products. Urea C13 API Price is not always fixed or binding as the Urea C13 Price is obtained through a variety of data sources. The Urea C13 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MERETEK UBT KIT (W/ PRANACTIN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MERETEK UBT KIT (W/ PRANACTIN), including repackagers and relabelers. The FDA regulates MERETEK UBT KIT (W/ PRANACTIN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MERETEK UBT KIT (W/ PRANACTIN) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A MERETEK UBT KIT (W/ PRANACTIN) supplier is an individual or a company that provides MERETEK UBT KIT (W/ PRANACTIN) active pharmaceutical ingredient (API) or MERETEK UBT KIT (W/ PRANACTIN) finished formulations upon request. The MERETEK UBT KIT (W/ PRANACTIN) suppliers may include MERETEK UBT KIT (W/ PRANACTIN) API manufacturers, exporters, distributors and traders.
click here to find a list of MERETEK UBT KIT (W/ PRANACTIN) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The MERETEK UBT KIT (W/ PRANACTIN) Drug Master File in Japan (MERETEK UBT KIT (W/ PRANACTIN) JDMF) empowers MERETEK UBT KIT (W/ PRANACTIN) API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the MERETEK UBT KIT (W/ PRANACTIN) JDMF during the approval evaluation for pharmaceutical products. At the time of MERETEK UBT KIT (W/ PRANACTIN) JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of MERETEK UBT KIT (W/ PRANACTIN) suppliers with JDMF on PharmaCompass.
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