25 Aug 2022

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Tender// Capecitabine (500 mg) Tablets needed in Poland [ENA14801]
Swietokrzyskie Cancer Center Independent Public Healthcare is looking for supplies of Capecitabine (500 mg) Tablets for commercial purpose. The required quantity is 1,300 units. The deadline is 20-Sep-2022.

Comments :

chowdary@carbontree.in

Dear Sir,
We have ready stocks Capacitabine 500mg from our EUGMP certified facility.
Please send your enquiry bd@spaccurelabs.com
www.spaccurelabs.com
Hyderabad, India

11:07,  25 Aug 2022

tianranbiotechz@gmail.com

Our company is located in Uganda, Africa. The factory directly supplies medical bovine skin gelatin, which is suitable for capsules, soft gel, etc. welcome to negotiate and cooperate.
We are a manufacturer with many international certifications, including FDA, ISO 22000, FSSC22000, Halal, GMP, BRC and other certifications.

tianranbiotechz@gmail.com

13:29,  25 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

11:40,  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

18:10,  07 Sep 2022
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