Reply
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
sidpatel6389@gmail.com
SIDDHA PHARMACY is presently one of India’s leading stockiest, Branded Pharmaceutical Exporter and Pharma Merchant Exporter for Private Label Pharma Manufacturing. Being a Branded Pharma Exporter we provide 100% original and are manufactured by well-known pharmaceutical manufacturers like Pfizer Inc, Novartis, GlaxoSmithKline Plc, Sanofi, Bayer AG, Eli Lilly and Co, Roche... We have our biggest market in EMEA as Branded Pharma Exporter and Branded Medicine Exporter owing to our quality service and best prices provided to our customer. We also work with clusters of manufacturers for White Label Manufacturing having the following certification: WHO GMP, EU-GMP, PIC/s, UKMHRA etc.
SIDDHA PHARMACY
SIDPATEL6389@GMAIL.COM
WWW.SIDDHAPHARMA.COM
WWW.SIDDHAGLOBAL.COM
GSTIN – 24ACWFS1209B1ZB
IEC CODE – ACWFS1209B
CONTACT NO. / WHATSAPP NO. - +91-8866 86 2020
enquiry@healthbiotech.in
Hello There,
Greetings from Health Biotech Limited!
We are one of the leading Indian Pharmaceutical Manufacturer & Exporter of finished formulations. Our state-of-the-art, WHO-GMP certified manufacturing
facilities are located in the industrial town of Baddi, in the State of Himachal Pradesh, India.We are a global exporter and currently export to more than 51 countries.
Kindly contact us +91 987-688-2973 or send email enquiry@healthbiotech.in
Thanks,
Health Biotech Limited
Phone : +91 987 688 2973
Email : enquiry@healthbiotech.in
Website : www.healthbiotech.in
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
pooja.arane@zenvisionpharma.com
I am Pooja Arane working with Zenvision Pharma LLP .
Please contact :pooja.arane@zenvisionpharma.com
Mob.no-9137027167
As a capability we can support the development for all formulation dosages forms (Liquid, Sterile form
Injectables, Otic & Ophthalmic Preparations, Oral Solids,LiquidsTopical & NDDS) up to Tech Transfer.
Zenvision Pharma LLP is a contract research & development organization based in Navi Mumbai, India; offering full range of custom designed formulation development services with professional standards. We offer turnkey product development services for Generic and Specialty pharmaceuticals.
ivyding@drughk.com
We can provide AVATROMBOPAG API , also we have finished validated pilot production , if you have the requirement ,pls contact with me .
