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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
gauravkumar4368@gmail.com
Dear Sir / Madam,
We can offer Naproxen Sadium API. Kindly let us know your email id so that we can send you the email and we can give you the best price.
Please sent the email following email address.
gauravkumar4368@gmail.com
Best Regards,
Gaurav Kumar
Indo Pharm
INDIA
bdevomaar@gmail.com
Dear
Please send your inquiry on below email.
We can support your requierment for the API with all documents for registration.
bdevomaar@gmail.com.
Kind regards
bdevomaar@gmail.com
Dear
Please send your inquiry on below email.
We can support your requierment for the API with all documents for registration.
bdevomaar@gmail.com.
Kind regards
sr@nikolospharma.com
We are interested to supply
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
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.
"
heliantus@heliantus-milano.it
Dear Sirs,
We have this API in stock in Italy for pormpt shipment. Can you contact HELIANTUS SRL, in Italy.
Our mail are:
marco_sgaravatti@hotmail.com
heliantus@heliantus-milano.it
Thank you & bst regards
Marco
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