26 Aug 2022

Reply

Tender// Various Finished Dosage Formulations needed in Poland [ENA14812]
National Institute of Oncology named after Marii Sklodowskiej-Curie - National Research Institute is looking for supplies of Various Finished Dosage Formulations for commercial purpose. The deadline is 19-Sep-2022.
1. Human Albumin (20% in 100 ml) Injections. The required quantity is 7,000 units.
2. Lactobacillus Rhamnosus (10 MLD CFU) Capsules. The required quantity is 6,000 units.

Comments :

overseasales2@yongstandards.com

Youngxin Pharm is a listed supplier of TEVA, Gedeon Richter, KRKA, etc, specialized in reference standards and drug impurity standards field. We've got more than 600,000 different kinds of products in the catalog. Kindly reach me at overseasales2@yongstandards.com. Hope we can do something for you.

11:29,  26 Aug 2022

drniral@medwiseoverseas.com

Dear Sir/Madam,
Greetings of the day!!
We can surely provide required product. Kindly let us know how we can proceed further for the same.

Thanks & Regards

11:39,  26 Aug 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

09:31,  30 Aug 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 kindly contact us for the mentioned requirement.

Thanks,

Jay
Health Biotech Limited
+91 987-688-2973
enquiry@healthbiotech.in
www.healthbiotech.in

18:09,  07 Sep 2022
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