11 Nov 2024

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Silymarin (1.2 MT - 1.4 MT/ annum) API needed in India [ENA21083]
A company that focuses on the development and manufacturing of various nutraceutical products is looking for suppliers of Silymarin (1.2 MT - 1.4 MT/ annum) API for commercial purposes. The suppliers must support this enquiry with CEP, GMP & CoA.

Comments :

foramjjani@gmail.com

Hello,
Greetings of the day. Can contact +919819435009 for dmf, dossier & regulatory/QA documents.

17:47,  11 Nov 2024

vishvesh.shaishav@gmail.com

We are focussed on developing new manufacturing technologies, including custom synthesis of new moleculepharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, pharmaceutical pellets,additives, contract manufacturing, chemicals. We began in the field of specialty intermediates for pharmaceutical applications and developed our own purification technologies for manufacturing highly pure intermediates. And Pharmaceutical API At a later stage, we integrated forward to manufacture finished formulations for both veterinary and human consumption. Due to our completely integrated operations in the pharmaceutical sector, we continuously learn about the quality parameters for an API based on the performance of the finished formulation in order to quality their Bioequivalence Studies.?We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.?Our focus lies in developing new production technologies with a keen interest in frugal innovation in order to gain a competitive edge over others. We specialize in the custom synthesis of molecules and work with many reputed companies around the world on an OEM basis.pharmaceutical pellets,Intermidiates ?Our finished formulations from WHO-GMP and EU-GMP units are registered/being registered in 26 countries within Asia, Europe, North America, Latin America and Africa continents including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad, Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.?vishvesh.shaishav@gmail.com
+919725487108
+919726387108

19:33,  11 Nov 2024

info@biopharmacentrum.com

Hi,
We can supply this product, having cost effective and quality & regulatory complied. Please send your inquiry for any products at "info@biopharmacentrum.com" or Whatspp +91 89514 33372
Thanks.

09:53,  12 Nov 2024
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