11 Nov 2024

Reply

USP Grade Sodium Picosulfate (2 kg) API needed in U.A.E [ENA21080]
A company that focuses on distribution of various pharmaceutical products is looking for suppliers of USP Grade Sodium Picosulfate (2 kg) API for commercial purposes. The suppliers must support this enquiry with DMF & CoA.

Comments :

foramjjani@gmail.com

Hello,
Greetings of the day. Can contact +919819435009 for dmf, dossier & regulatory/QA documents.

17:48,  11 Nov 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

19:34,  11 Nov 2024

hostrinlifesciences@gmail.com

Dear Friends,

Greetings from Hostrin Life Sciences!!!

Hostrin offers the following services:

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

CDMO (Contract research, development and manufacturing organisation) activity and growing rapidly. Offering drug product development services from Active pharmaceutical ingredient to Formulation development and manufacturing for all the markets with relevant regulatory requirements.

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

02:02,  12 Nov 2024

kawtarettayri@zintellec.com

Dear Sir/Madam,
I hope this message finds you well.
ZIntellec Chemical is a reliable Chinese supplier of high-quality APIs and pharmaceutical intermediates, catering to the global pharmaceutical and compounding industries. We are dedicated to delivering premium products, backed by full documentation to ensure both quality and compliance.

We would be delighted to explore how we can meet your business needs and collaborate on future projects.

Best regards,
Kawtar

06:47,  12 Nov 2024

kawtarettayri@zintellec.com

Dear Sir/Madam,
I hope this message finds you well.
ZIntellec Chemical is a reliable Chinese supplier of high-quality APIs and pharmaceutical intermediates, catering to the global pharmaceutical and compounding industries. We are dedicated to delivering premium products, backed by full documentation to ensure both quality and compliance.

We would be delighted to explore how we can meet your business needs and collaborate on future projects.

Best regards,
Kawtar

06:53,  12 Nov 2024

info@biopharmancetrum.com

Hi,
We can supply this product, having cost effective and quality & regulatory complied. Please send your inquiry for any products at "info@biopharmacentrum.com" or Whatspp +91 89514 33372
Thanks.

09:54,  12 Nov 2024

contact@clearsynthlabs.com

Reply: USP Grade Sodium Picosulfate 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 inquiries.

Regards
17, Lotus Business Park
Andheri West
Mumbai - 400 053
Maharashtra State
Tel/WhatsApp: +91-9233671546
contact@clearsynthlabs.

14:30,  16 Nov 2024
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