03 Jan 2024

Reply

Polymyxin B Sulfate API needed in Russia [ENA18851]
A CRO that focuses on providing a full package of services for drug registration, pharmacovigilance, preclinical studies and all phases (I-IV) of clinical trials is looking for suppliers of Polymyxin B Sulfate API for development purposes. The required quantity is 500 grams for development and 10 kg/ annum for commercial purposes. The suppliers must support this enquiry with GMP, DMF & CoA.

Comments :

gauravkumar4368@gmail.com

Dear Sir / Madam,

We can offer APIs along with the supporting documents.Kindly let us know your email id so that we can send you the email and we can give you the best price.

Best Regards,
Gaurav Kumar
gauravkumar4368@gmail.com
Indo Pharm
INDIA

11:20,  03 Jan 2024

luisa.goglia@fischer-group.ch

Dear All,

We can offer you polymixyin b with documentation.
Kindly contact us. Fischer chemicals AG in Zürich

13:55,  03 Jan 2024

sam.d@micoson.com

We will provide quotation and document support, please send an email to sam.d@micoson.com, we will reply in time. Thank you.

14:26,  03 Jan 2024

service5@dragonpharm.com.cn

Hangzhou Dragonpharm can supply this API

07:43,  04 Jan 2024

luisa.goglia@fischer-group.ch

Please contact me
We have DMF and GMP for this API!
Thank you Luisa Goglia

18:06,  04 Jan 2024

bdevomaar@gmail.com

Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents for registration.
bdevomaar@gmail.com
Kind regards

14:19,  06 Jan 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

21:55,  08 Jan 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

21:56,  08 Jan 2024

export3@zealmp.com

Dear Sir, Greetings from Zeal Medipharma Export India.
We are Government of India Recognized Star Export House based in Mumbai India, currently exporting wide range of APIs to more than 40 countries.
Please send your valuable purchase inquiry on export3@zealmp.com. We will be glad to submit our best offer.

Best Regards,
Ashvi Panchal
Business Development
Zeal Medipharma
(EXPORT) PRIVATE LIMITED
Mumbai, India
Tel: +91-22-25836688
Mobile : +91 9867166055
E-mail : export3@zealmp.com

11:31,  23 Jan 2024

contact@clearsynthlabs.com

Reply: Polymyxin B Sulfate 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

04:51,  02 Feb 2024
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