20 Aug 2022

Reply

Tender// Various Finished Dosage Formulations needed in Poland [ENA14747]
Mazowiecka Instytucja Gospodarki Budzetowej Mazovia is looking for supplies of Various Finished Dosage Formulations for commercial purpose. The deadline is 22-Sep-2022.
1. Ibuprofen (200 mg) Tablets. The required quantity is 3,840 units.
2. Ascorbic Acid (200 mg) Tablets. The required quantity is 2,400 units.
3. Paracetamol (500 mg) + Diphenhydramine Hydrochloride (25 mg) Tablets. The required quantity is 3,240 units.

Comments :

sam.d@micoson.com

Micoson Biopharma can provide it, please send mail to sam.d@micoson.com. We will provide documents and quotations promptly.

20:02,  20 Aug 2022

temad@temad.com

Dear Sir, We are able to supply Finished dosage forms.Please inform us your email address to have more negotiation.

12:36,  21 Aug 2022

muming@jemincare.com

dear friend, we may provide you with the required products. please contact muming@jemincare.com

08:20,  22 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

14:46,  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 +91 987-688-2973 or send email enquiry@healthbiotech.in

Thanks,

Jay
Health Biotech Limited
www.healthbiotech.in

17:04,  07 Sep 2022

NouryonChemltd@gmail.com

We can supply quality Ascorbic acid from the USA at a competitive market price with fast delivery. Feel free to contact us for your order inquiry Nouryonchemltd AT gmail DOT com
Skype ID: NouryonChemltd

17:16,  15 Dec 2022
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