09 Jun 2022

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Tender// Various Finished Dosage Formulations needed in Poland [ENA13912]
Szpital Powiatowy w Zambrowie Sp. z o. o is looking for supplies of Various Finished Dosage Formulations for commercial purpose. The deadline is 14-Jul-2022.
1. Cefuroxime (1.5 g) Injections. The required quantity is 20,000 units.
2. Omeprazole (40 mg) Injections. The required quantity is 6,000 units.

Comments :

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), 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

16:32,  09 Jun 2022

marketing.neion@gmail.com

Hello
Please share your contact details to discuss further.

13:14,  10 Jun 2022

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

14:44,  13 Jun 2022

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. We frequently export to regions like CIS, LATAM, Middle East, Africa, South Asia and many more.


Our Product Range :
Dry & Liquid Injectables, Pre-Filled Syringes, Betalactum Injectables, Tablets, Capsules, Soft Gelatin Capsules, Dry Syrups, Liquid Orals,
Eye/Ear Drops, Effervescent & Mouth Dissolving Tablets, Ointments, Dental Cartridges, Suppositories, IV Fluids

Our Product Category :
Anti Covid19, Anti Retro Virals, Anti Biotics, Anti Fungal, Cardiovascular, Gastrointestinal, Hormones, Oncology, Veterinary

Our Services
PCD Pharma Franchise, CRAMS / Contract Manufacturing, Loan Licensing, Institutional sale, Technology Transfer etc.


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

10:50,  15 Jun 2022

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

18:37,  20 Jun 2022
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