Veranova: A CDMO that manages complexity with confidence.
01 1Macfarlan Smith Limited
01 1Methylphenidate Hydrochloride
01 1U.S.A
Veranova: A CDMO that manages complexity with confidence.
Registration Number : 302MF10009
Registrant's Address : 10 Wheatfield Road, Edinburgh EH11 2QA, United Kingdom
Initial Date of Registration : 2020-01-17
Latest Date of Registration : 2020-01-17
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PharmaCompass offers a list of Methylphenidate Hydrochloride 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 Methylphenidate Hydrochloride manufacturer or Methylphenidate Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methylphenidate Hydrochloride manufacturer or Methylphenidate Hydrochloride supplier.
PharmaCompass also assists you with knowing the Methylphenidate Hydrochloride API Price utilized in the formulation of products. Methylphenidate Hydrochloride API Price is not always fixed or binding as the Methylphenidate Hydrochloride Price is obtained through a variety of data sources. The Methylphenidate Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Quillivant xr (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quillivant xr (TN), including repackagers and relabelers. The FDA regulates Quillivant xr (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quillivant xr (TN) 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 Quillivant xr (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quillivant xr (TN) supplier is an individual or a company that provides Quillivant xr (TN) active pharmaceutical ingredient (API) or Quillivant xr (TN) finished formulations upon request. The Quillivant xr (TN) suppliers may include Quillivant xr (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Quillivant xr (TN) 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 Quillivant xr (TN) Drug Master File in Japan (Quillivant xr (TN) JDMF) empowers Quillivant xr (TN) 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 Quillivant xr (TN) JDMF during the approval evaluation for pharmaceutical products. At the time of Quillivant xr (TN) 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 Quillivant xr (TN) suppliers with JDMF on PharmaCompass.
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