21 Oct 2022

Reply

Tender// Various Finished Dosage Formulations needed in Sweden [ENA15389]
Region Jonkoping County is looking for supplies of Various Finished Dosage Formulations for commercial purpose. The deadline is 15-Nov-2022.
1. Fidaxomicin (200 mg) Tablets. The required quantity is 2,920 units.
2. Clonidine (150 mcg/ ml) Injections. The required quantity is 11,330 units.
3. Rifampicin (300 mg) Capsules. The required quantity is 24,200 units.
4. Mepivacaine (10 mg/ ml) Injections. The required quantity is 13,600 units.

Comments :

smit@salvavidaspharma.com

Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers of pharmaceutical products.
can we connect for some business?

Please, contact
smit@salvavidaspharma.com
Mo: +91 74359 19702 (Whatsapp : https://wa.link/8hjiee )
(Telegram : https://t.me/smit_slavavidas )

11:07,  21 Oct 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

For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343

12:15,  22 Oct 2022

sales03@jnchsd.com

We are leading pharmaceutical manufacturer from China on APIs and intermediates, Mepivacaine is availiable with good quality and nice price. Please reach at sales03@jnchsd.com for any enquiry.
Best regards

10:59,  09 Dec 2022

sales03@jnchsd.com

We are leading pharmaceutical manufacturer from China on APIs and intermediates, Mepivacaine is availiable with good quality and nice price. Please reach at sales03@jnchsd.com for any enquiry.
Best regards

10:59,  09 Dec 2022
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