Bal Pharma, leading manufacturer of niche & specialty API, Intermediates and Finished Formulations.
01 1M/s Bal Pharma Limited
02 1M/s Glenmark Life Sciences Limited
03 1M/s Jubilant Pharmova Limited
04 1M/s MSN Laboratories Private Limited
05 1M/s Megafine Pharma (P) Limited
06 1M/s. Alkem Laboratories Ltd.
07 1M/s. Cadila Pharmaceuticals Ltd.,
08 1M/s. Cipla Limited
09 1M/s. Mylan Laboratories Ltd.,
10 1M/s. Unimark Remedies Limited
Bal Pharma, leading manufacturer of niche & specialty API, Intermediates and Finished Formulations.
Date of Issue : 2022-08-25
Valid Till : 2025-07-02
Written Confirmation Number : WC-0156
Address of the Firm : 61-B, Bommasandra Industrial Area, Bengaluru-560 099, India
99
PharmaCompass offers a list of Paliperidone 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 Paliperidone manufacturer or Paliperidone supplier for your needs.
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A Invega Sustenna manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Invega Sustenna, including repackagers and relabelers. The FDA regulates Invega Sustenna manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Invega Sustenna 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 Invega Sustenna supplier is an individual or a company that provides Invega Sustenna active pharmaceutical ingredient (API) or Invega Sustenna finished formulations upon request. The Invega Sustenna suppliers may include Invega Sustenna API manufacturers, exporters, distributors and traders.
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A Invega Sustenna written confirmation (Invega Sustenna WC) is an official document issued by a regulatory agency to a Invega Sustenna manufacturer, verifying that the manufacturing facility of a Invega Sustenna active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Invega Sustenna APIs or Invega Sustenna finished pharmaceutical products to another nation, regulatory agencies frequently require a Invega Sustenna WC (written confirmation) as part of the regulatory process.
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