15 Sep 2023

Reply

Tender// Various Finished Dosage Formulations needed in Moldova [ENA18040]
Center for Centralized Public Procurement in Health is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 11-October-2023.
1. Valproic Acid (300 mg) Tablets. The required quantity is 126,440 units.
2. Amisulpride (200 mg) Tablets. The required quantity is 77,870 units.

Comments :

sales@royalbiotech.co.in

We shall provide Sodium Valproic acid tablet and Amisulpride tablet from EUGMP approved site. Contact us at sales@royalbiotech.co.in

17:45,  15 Sep 2023

sam.d@micoson.com

Please send an email to sam.d@micoson.com and we will provide quotation and document.
Thank you.

19:40,  16 Sep 2023

hostrinlifesciences@gmail.com

Dear Friend,

Greetings from Hostrin Life Sciences!!!

Hostrin offers the following services:

1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.

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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.

3. Support for Impurity's, Reference standards and RLD's

4. Services for IPR & Regulatory compliance with all risk assessments.

5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.

6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.

7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.

8. Synthetic Resin technologies support.

9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.

10. 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
www.hostringlobal.com

19:56,  16 Sep 2023

kunder@bio-synth.co

INTRODUCTION - API & INTERMEDIATES
Me
Wed, 10 Apr 2024 3:33:37 PM +0530
"makpharma4"
Dear sir/Madam,

Greetings from Bio-synth!

We, Biochemical and Synthetic Products Private Limited, INDIA introduce ourselves as one of the leading manufacturers and exporters of various API & Intermediates. Our Plant is accredited with an ISO Certified and also cGMP Compliant with an Installed Capacity of 500 MT per annum.

We are manufacturing below API in our GMP plant

?
1. AMISULPRIDE IP/BP

2. CARVEDILOL IP/BP/USP/EP

3. METOCLOPRAMIDE HCL IP/BP/EP/USP

4. RIVAROXABAN

5. SODIUM AMINO SALICYLATE

6. 4-AMINO SALICYLIC ACID USP(PAS ACID USP)

7. ETHOPABATE BP VET

8. BILASTINE

9. BEDAQUILINE?
?

Presently, we have supplying our API & Intermediates to our domestic and International customers for the past several years.

We enclose herewith our updated API & Intermediates list which we are currently manufacturing in our GMP Plant.

Now we request you to please let us know your requirements to enable us to offer our competitive price



Thanks and regards,

Purushotham Kunder
Dy. Manager
Biochemical and Synthetic Products Pvt. Ltd
Mumbai /Hyderabad
Ph. No./Whatsapp no. +91-9869455944
Email: kunder@bio-synth.com

16:18,  10 Apr 2024
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