04 Mar 2024

Reply

Various Excipient needed in Mexico [ENA19135]
A MNC which focuses on manufacturing and distribution of various health, hygiene & nutrition products is looking for suppliers of various excipient for commercial purposes. The supplier must support this enquiry with GMP & CoA.
1. Sodium Edetate (2,700 kg) Excipient
2. Xanthan gum (8,050 kg) Excipient

Comments :

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, 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.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

15:19,  04 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

22:54,  04 Mar 2024

Cristonelifecare@gmail.com

Dear Friend,

Greetings from Hostrin Life Sciences!!!

Hostrin offers the following services:

1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.

Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/FDA with 5 modules including BA and BE studies /Clinical studies/trials for finished formulation's in Pharmaceutical, ayurveda, Biotech, Biosimilar, vitamins , Peptides and Transdermal patches too.

2. eCTD publishing with potential softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.

3. Support for Impurity's, Reference standards and RLD's

4. Services for IPR & Regulatory compliance with all risk assessments.

5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.

6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.

7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.

8. Synthetic Resin technologies support.

9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.

10. Pharmacovigilance services.

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

For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com

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

23:28,  05 Mar 2024

sales@raycepharma.com

Greeetings from RAYCE PHARMA!
We can provide the required api along with documention and at best and competitive prices.

Kindly send your inquiry on sales@raycepharma.com

Thank You!

12:08,  07 Mar 2024

gauravkumar4368@gmail.com

Dear Sir / Madam,

We can offer variuos 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

15:41,  12 Mar 2024

vikash@sugamts.com

Hii. We have earlier supplied Paracetamol in large 60 Tons batch to Mexico. Well aware of local requirement and processes. We have facilities making best class excipients and can meet both your requirements. And the facility is WHOGMP approved. You can write to us with exact requirement, timeline and we will get back within 24 hrs.

17:12,  21 Mar 2024

ethan@unipolymer.com

Hello Sir, we are manufacturer of Povidone excipients, also we can supply many other API and Excipients, please feel free to contact me for any new inquiry.

11:41,  31 Mar 2024

albert@sybiochem.com

we can support

11:08,  06 Apr 2024

Pur3@sigachi.com

We can supply all Excipients and API required for your formulation

17:46,  24 Apr 2024

ethan@unipolymer.com

Hello we are Povidone manufacturer from China, and we also supply many other excipients, please feel free to contact me by email. Or WhatsApp

17:53,  24 Apr 2024

exports@krishkan.com

Dear Sir,

We are pleased to introduced as reputed India based API & Excipient exporters and partners to a large number of Pharma companies across many countries.

Kindly write to us for any Excipients or APIs to exports@krishkan.com

Thanks and regards,
SMITHA

17:58,  26 Apr 2024

contact@clearsynthlabs.com

Reply:
1. Sodium Edetate Excipient
2. Xanthan gum Excipient

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

05:37,  02 May 2024
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