26 Oct 2024

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USP Grade Semaglutide API needed in the U.S.A [ENA20968]
A compounding pharmacy specializing in the preparation of various health and nutrition finished formulations is looking for suppliers of USP Grade Semaglutide API for commercial purposes. The suppliers must support this enquiry with USDMF & CoA.

Comments :

haoran.tse@gmail.com

Chengdu Pukang is the largest manufacturer of side chain intermediates for long-acting polypeptide drugs such as semaglutide & tirzepatide in China. We can supply api along with all the docs for you.

22:31,  26 Oct 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

23:15,  26 Oct 2024

foramjjani@gmail.com

Hello,

Greetings for the day!

My name is Foram Jani.

Regulatory: I provide end to end product registration services like compiling a dossier ECTD format based on country-specific requirements as well as query resolution. I can also prepare DMF, PV, COA, FPS and all pharma technical documents.

Looking forward for a positive response.

Warm Regards,

Ms. Foram Jani

Regulatory affairs specialist

Mumbai, Andheri, India
WhtsApp: +919819435009
Email: foramjjani@gmail.com

14:07,  27 Oct 2024

emanuel@cainepharma.com

Hi,
We are located in Florida. We can provide Semaglutide for you. What is the minimum order quantity? We have a lead time of greater than 6 days .We can also provide COA and other accreditation. Email me: emanuel@cainepharma.com

20:41,  30 Oct 2024
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