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bdevomaar@gmail.com
Dear
Please send the inquiry on below email.
We can support your requierment for the API.
bdevomaar@gmail.com
Best 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 looking forward to your early reply to establishing a business relationship with your company.
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
exim@maithililifesciences.com
We are a pharmaceutical manufacturing company in India into Api and advanced intermediates
www.maithililifesciences.com
Please reach us at exim@maithililifesciences.com
info@maithililifesciences.com
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
manickt@aamangeniushealthcare.co.in
HI
EPHIDRINE HCL needs import permit from your MOH as per quota allotted and updated in INCB followed woth your p.o with notification for e signed issued permit whoch takes 90 days followed by PEN by our CBN .If you are ready with the above , plz send me mail manickt@aamangeniushealthcare.co.in.
Thanks
Manick.T
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`
Hi,
We can supply Ephedrine HCL API at a good price and good quality. What documents you will need apart from COA.
Pharm4you@vip.163.com
We are professional on supplying the APIs from China, but since the time is long time passed, does your esteemed company still have the interests to the Ephedrine? Looking forward to your reply.
Zhejiang Syntech Pharm Co., Ltd.
Add: Xianghe Rd. 178, Anji, Huzhou City, Zhejiang, China
Wechat : Pharm4you
Email : Pharm4you@vip.163.com
Mobile : 008613857259937
