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crystalchemicalsfzllc@gmail.com
We can supply the following API, Please contact
Crystal Chemicals FZ-LLC
FDRK-3517, PO Box # 10055, Ras-AL-Khaimah, United Arab Emirates
Mobile & (Whatsapp) +92-333-8484130
E: crystalchemicalsfzllc@gmail.com
W: www.crystalchemicals.com.pk`
bdevomaar@gmail.com
Dear
Please send the inquiry on below email.
We can support your requierment for the API injectable grade with CTD DMF.
bdevomaar@gmail.com
Kind regards
SALVAVIDAS PHARMACEUTICAL PVT.LTD
We are A Reputed Pharmaceutical Product manufacturer, Exporter, and Export of various types of Pharmaceutical Products throughout the world.
We are dealing in Active Pharmaceutical Ingredients (API’s), Veterinary APIs, Intermediates, Excipients & Chemicals… We deal with Branded Drugs along with all Related Documents and Certificates.
We have a wide range of Medicines like Antibiotics, Cardio diabetics, Anti-Cancer, Nutraceuticals & Many more.
We are always there to serve you with our best services
All Products are Manufactured in WHO, GMP, ISO 9001 certified manufacturing units.
Best Regard.
Rohan Patel
Business Development Executive
Email- rohan@salvavidaspharma.com
Whatsaap- +91-9313237877
Web: www.salvavidaspharmaceutical.com
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 APPROVE
pharmahouse@ymail.com
We will supply Beta-carotene food grade.please let me know powder form or oil form with % required.
Pharma House
Hyderabad, India
pharmahouse@ymail.com
+91 8143369525
harshad976@gmail.com
"Greetings for the day !
I take this opportunity to write to you with introduction of our Pharmaceuticals company same established in year 2007 and we have valid approval like US-FDA, UK-MHRA, Anvisa, TGA, WHO-GMP Etc.
We offer API, Intermediates and FDF products from Regulatory approved plant.
"
shplexim@sohanhealthcare.com
Hi,
Sohan Healthcare Pvt Ltd is engaged in manufacturing of Active Pharmaceuticals Ingredients, Semi Finished formulations. The facility is audited and approved by European Authority, Russian Authority, Korea MFDS. Our facility is also USFDA complied. We hold CEP for Metformin HCl API. SHPL exports products to more than 30 countries and has more than 100 satisfied customers.
Our product details as per below
Metformin HCL EP/BP/IP/USP/CEP
Metformin DC Granules 86.66% / 93.60% / 95% / 90% / 83.33%.
Gliclazide EP/BP/IP/CEP
Folic Acid- IP, USP
(TTBB) 3- tripheny1-methy1-5(4-bromo methy1)(1,1 bipheny1)-4y1-1 H-Tetrazole.
Best & Regards,
Ramnath Pachpind
Mo +91-8552057638
shplexim@sohanhealthcare.com
Sohan Healthcare Pvt Ltd
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
