07 Mar 2024

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Cannabidiol (25 g - 50 g) API needed in India [ENA19161]
A research-driven company that focuses on custom synthesis of pharmacopeial & non-pharmacopeial reference standards is looking for suppliers of Cannabidiol (25 g - 50 g) API for development purposes. The suppliers must support this enquiry with CoA.

Comments :

vssahu77741@gmail.com

we can provide

01:07,  08 Mar 2024

vssahu77741@gmail.com

we can provide

01:07,  08 Mar 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

23:42,  10 Mar 2024

AAmbrosi@Noramco.com

With more than 300 commercial reference standards in stock, Purisys provides structural elucidation and comprehensive characterization data for your development and commercial requirements in support of regulatory filings and drug product releases.

Purisys has a specialized process to support rapid development and qualification of standards. We can support you by providing custom synthesis of degradation products, metabolites, and other unique impurities.
Anthony Ambrosini
2153509795

19:20,  25 Apr 2024

contact@clearsynthlabs.com

Reply: Cannabidiol API

Clearsynth Labs is Manufacture/Wholesale Supplier of WHO cGMP, ISO, and GMP quality APIs, Intermediates, Excipients… with CoA, Chemical research… and services from India, UAE, Europe, Canada, US that meet customer and regulatory requirements (USDMF/CEP) compliance at a competitive price. Kindly contact us for your requirement.

Regards
17, Lotus Business Park
Andheri West
Mumbai - 400 053
Maharashtra State
Tel/WhatsApp: +91-8074411410
contact@clearsynthlabs.com

05:19,  02 May 2024
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