14 Nov 2024

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Sodium Carboxymethylcellulose (5 MT) API needed in Russia [ENA21118]
A company that focuses on the distribution of various pharmaceutical products is looking for suppliers of Sodium Carboxymethylcellulose (5 MT) API for commercial purposes. The suppliers must support this enquiry with CoA.

Comments :

luisa.goglia@fischer-group.ch

Plase contact Fischer Chemicals AG in Switzerland.
Thank you.

16:41,  14 Nov 2024

info@aeqpharma.com

We have Carboxymethylcellulose API along full support docs
info@aeqpharma.com

17:12,  14 Nov 2024

avinash@dvsrlifesciences.com

Dear Sir/Madam

We can Supply Sodium Carboxymethylcellulose with the proper Documentation can we connect and discuss this further?

Thank you,

Avinash Devireddy
E: avinash@dvsrlifesciences.com
Mobile/WhatsApp: +91 9121391234.

19:58,  14 Nov 2024

kawtarettayri@zintellec.com

Dear Sir/Madam,
I hope this message finds you well.
ZIntellec Chemical is a reliable Chinese supplier of high-quality APIs and pharmaceutical intermediates, catering to the global pharmaceutical and compounding industries. We are dedicated to delivering premium products, backed by full documentation to ensure both quality and compliance.

We would be delighted to explore how we can meet your business needs and collaborate on future projects.

Best regards,
Kawtar
http://www.zzhxchem.com

09:42,  15 Nov 2024

marketing@hengkangpharm.cn

zhejiang hengkang group can supply.

15:30,  15 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

08:29,  16 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

08:30,  16 Nov 2024

sam.d@micoson.com

We are Micoson Biopharm Co,.Ltd company from China. We will provide quotation and document support, please send an email to sam.d@micoson.com, we will reply in time. Thank you.

20:56,  17 Nov 2024
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