27 Sep 2022

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Tender// Anakinra (100 mg/ 0.67 ml) Injections needed in Poland [ENA15135]
Provincial Specialist Children's Hospital st. Ludwika w Krakowie is looking for supplies of Anakinra (100 mg/ 0.67 ml) Injections for commercial purpose. The required quantity is 120 units. The deadline is 7-Oct-2022.

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sales@clearsynthlab.com

Reply: Anakinra (100 mg/ 0.67 ml) Injections

Clearsynth demonstrates the ability to consistently manufacture APIs, Intermediates, Chemical research… and services that meet customer and regulatory requirements. Kindly confirm your requirement by email so we can provide the Quotation, COA within 24hrs Max from the inquiry date.

Regards

Mr. V. Ambati
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
Tel/WhatsApp : +91-9394436878
sales@clearsynthlab.com

15:44,  28 Sep 2022

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 )

17:52,  28 Sep 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

19:16,  29 Sep 2022

indiastar2210@gmail.com

Dear Sir/Madam
We, the undersigned, offer to provide the technical consulting services for formulation and development of sterile injection, ophthalmic formulation (solution and suspension), Liquid oral solution and suspension products including finalisation of formula composition and finalisation of manufacturing process with reproducibility. support in trouble shooting activities during development and commercial projects.

12:08,  03 Nov 2022
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