Reply
1. Osimertinib API. The required quantity is 26 kg/ annum & later 37 kg/ annum.
2. Niraparib API. The required quantity is 36 kg/ annum & later 41.8 kg/ annum
3. Ixazomib API. The required quantity is 0.6 g/ annum & later 0.068 kg/ annum.
gauravkumar4368@gmail.com
Dear Sir / Madam,
We can offer all various APIs 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
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
Whatsapp +91 9033215377
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVE
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
554127759
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
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
bd@pharminterface.com
Dear Sir/Madam,
We can provide all APIs with their supporting documents. We can provide you with the best price. Plz go through our below website
Regards
Priya Patil
priya.p@pharminterface.com
https://pharminterface.com/
info@shreechemicalsimpex.com
Hello,
We, "SHREE CHEMICALS IMPEX " are contract manufacturer, supplier and exporter of active pharmaceutical ingredient, pharmaceutical intermediate and agrochemicals.
We can fulfill your requirements.
Please contact on following details.
E-mail : info@shreechemicalsimpex.com
Mo-no : (+91) 8000239721
pranavvaidya@farmson.com
Greetings!!
As you are aware Farmson Pharmaceutical, is the world leader manufacturer of Paracetamol / Acetaminophen API & DC Granules, with various regulatory approvals / certifications like ISO 9001: 2008, ISO 14001: 2004, ISO 18001: 2007, WHO GMP, TGA, CEP from EDQM, EU GMP, ENVISA etc. & DMF / Registrations in Japan, Korea, Russia, Ukraine, Uzbekistan etc.
Please share your requirements on pranavvaidya@farmson.com
smit@salvavidaspharma.com
Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers of pharmaceutical products.
can we connect for some business?
Please, contact
smit@salvavidaspharma.com
Mo: +91 74359 19702 (Whatsapp : https://wa.link/8hjiee )
(Telegram : https://t.me/smit_slavavidas )
info@aeqpharma.com
we sell all API with full support docs.
info@aeqpharma.com
sales@clearsynthlab.com
Reply:
1. Osimertinib API
2. Niraparib API
3. Ixazomib API
Clearsynth demonstrates the ability to consistently manufacture APIs, Intermediates, Chemical research… 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
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
Tel/WhatsApp : +91-9394436878
sales@clearsynthlab.com
pharm4you@vip.163.com
Hi, we can offer you these pointed APIs, but wondering if the GMP and EDMF are also mandatory for your client?
Zhejiang Syntech Pharm Co., Ltd.
Add: Xianghe Road 178, Dipu Town, Anji, Huzhou City, Zhejiang, China
Wechat: Pharm4you Kakao talk: Pharm4you Mobile: 008613857259937
Email: pharm4you@vip.163.com
