26 Aug 2022

Reply

Ivacaftor (1 kg) API needed in the United States [ENA14808]
A CDMO that focuses on the development, manufacturing and marketing of various pharmaceutical excipients, cosmetics & medical devices is looking for suppliers of Ivacaftor (1 kg) API for development purpose.

Comments :

sales6@iffect.com.cn

Greetings from Iffect Chemphar Co., Ltd!

We could supply Ivacaftor (873054-44-5) 98% at commercial quantity.
More information needed, please feel free to contact.

12:42,  26 Aug 2022

crystalchemicalsfzllc@gmail.com

We can supply the following API, Please contact

Crystal Chemicals FZ-LLC
(Pharmaceuticals API's Distributor in UAE)
FDRK-3517, PO Box # 10055, Ras-AL-Khaimah, United Arab Emirates
(Whatsapp) +92-333-8484130
crystalchemicalsfzllc@gmail.com
www.crystalchemicals.com.pk

12:45,  27 Aug 2022

Hi
We can provide the same as per your requirement. Please let us know if we can help you out.

12:46,  28 Aug 2022

sales@bozera.com

we can offer you Ivacaftor with good price. pls. kindly send us mail for more discussion. than you.
sales@bozera.com

06:36,  29 Aug 2022

hostrinlifesciences@gmail.com

Dear friend,

Greetings from Hostrin Life Sciences!!!

We have been supporting the following services.

1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA. DMF's for API's, 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 software, addressing post submission queries from all regulatory authorities and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.

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

4. Services for IPR & Regulatory compliance

5. 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.

6. Custom synthesis and contract manufacturing services

7. Synthetic Resins technologies support.

8. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.

9. Pharmacovigilance services.

Pls don't hesitate to send your inquiries. 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

09:33,  30 Aug 2022

sales@clearsynthlab.com

Re: Ivacaftor API

Clearsynth demonstrates the ability to consistently provide products and services that meet customer and regulatory requirements. Kindly confirm your requirement by email so we can provide the Quotation, COA within 24hrs Max from the inquiry date.

Regards

Mr. V. Ambati
International Sales & Business Development
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
+91-9394436878
sales@clearsynthlab.com
clearsynthlab.com

16:08,  02 Sep 2022
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