11 Feb 2021

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USP Grade Ciprofloxacin (1.2 MT/ annum) API needed in Brazil [ENA09713]
A pharmaceutical manufacturing company that specializes in injectables is looking for suppliers of USP Grade Ciprofloxacin (1.2 MT/ annum) API for development purposes. The suppliers must support this enquiry with CoA and GMP.

Comments :

info@indeximinternational.com

Indexim international, are one of the leading supplier, exporter and importer of Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard,, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements. Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian countries and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India . Also most of the products are from WHO cGMP , ISO , GMP manufacturers.

Indexim International
sales.indeximinternational@gmail.com
info@indeximinternational.com
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407

13:59,  11 Feb 2021

We are a Pharmaceutical Company from UAE and we can supply you.

Contact us: ph@alnamatalalamy.com

14:41,  11 Feb 2021

info@aeqpharma.com

HI,
pleasecontact usfor get our best quote for CMO.

16:23,  11 Feb 2021

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

22:24,  11 Feb 2021

support@carense.com

At Carense we see the ability to provide creative and innovative solutions to regulatory challenges as an integral part of our offering in providing custom solutions to innovative companies. We’ve used our extensive regulatory experience to work with our customers and to develop effective ways to manage multi-filings in multiple territories for example. It’s all part of providing a holistic service offering that’s designed to broadly support customers for their CMC requirements.
There is increasing demand for broad-based service providers who can provide customers with an extensive range of offerings. As such, Carense now provides an integral API service for sourcing and development, by bringing these capabilities together with our existing expertise in this space and our process development capabilities, we can provide customers with a more simplified and complete offering.

=================================
Carense Ltd
71-75 Shelton Street
London,
WC2H 9JQ
United Kingdom
Company No. 12378533
Telephone: 0208 945 3443
Email: support@carense.com
=================================

19:26,  12 Feb 2021

marketing@giapharma.in

Dear Sir/Madam,
Greeting..
Please write us.

07:42,  13 Feb 2021

waghelakpd@gmail.com

WE CAN PROVIDE

14:15,  15 Feb 2021

jgq@yangzijiang.com

jgq@yangzijiang.com

I am Justin from Yangtze River Pharmaceutical Group in China

APIs and FDF can be manufactured by our company.

We can also CMO

If you need them, please contact me by Tel., WhatsApp and Wechat: +86 15261051195
Email: jgq@yangzijiang.com

07:39,  19 Feb 2021

sam.d@micoson.com

we would like to participate in the quotation and Please send your email to sam.d@micoson.com. We will reply to the quotation within 7 hours,

Thanks for your support.

20:17,  19 Feb 2021

alicechan@huarizy.com

HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.

1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80

email address: alicechan@huarizy.com
phone number: +86 18820220687

07:56,  22 Feb 2021

hostrinlifesciences@gmail.com

Dear Friend,

Greetings from Hostrin Life sciences!!!

We have been supporting the following services.

1.We do support DMF for API, Tech transfer support and Registration of Dossiers in ROW/MOH /MHRA/EMEA/USA support in CTD, ACTD, eCTD and ANDA's formats with 5 modules including BA and BE studies /Clinical studies/trials for API's & Formulations in Pharmaceutical, Ayurveda, Biotech, Biosimilar, vitamins , Peptides and recently Transdermal patches too.

2. Impurity's & Reference standards support for API's

3. Services for IPR & Regulatory compliance

4. Services for QMS & supporting of QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars companies who are willing to enter into the Regulatory market which is mandatory to show for FDA.

5. Custom synthesis & Contract manufacturing services

6. Synthetic Resins technologies support

Pls don't hesitate to send your enquiry's. For your reference please go through our website www.hostringlobal.com

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343  

22:24,  01 Mar 2021
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