19 Jul 2022

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Various Finished Dosage Formulations needed in Myanmar [ENA14398]
A large pharmaceutical company based in India that focuses in various segments such as gynaecology, cardiovascular, diabetology, asthma, paediatric, CNS, GI and NSAIDs is looking for suppliers of Various Finished Dosage Formulations for commercial purpose. The suppliers must support this enquiry with ACTD dossier & WHO-GMP/ PICs.
1. Acotiamide (300 mg) + Rabeprazole (20 mg) Tablets
2. Acotiamide (100 mg) Tablets
3. Flupirtine Maleate (400 mg) SR Tablets
4. Rifaximin (200 mg, 400 mg & 550 mg) Tablets
5. Tirofiban (5 mg/ 100 ml) Injections

Comments :

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
Whatsapp +91 9033215377
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVE

17:47,  19 Jul 2022

sidpatel6389@gmail.com

SIDDHA PHARMACY is presently one of India’s leading stockiest, Branded Pharmaceutical Exporter and Pharma Merchant Exporter for Private Label Pharma Manufacturing. Being a Branded Pharma Exporter we provide 100% original and are manufactured by well-known pharmaceutical manufacturers like Pfizer Inc, Novartis, GlaxoSmithKline Plc, Sanofi, Bayer AG, Eli Lilly and Co, Roche... We have our biggest market in EMEA as Branded Pharma Exporter and Branded Medicine Exporter owing to our quality service and best prices provided to our customer. We also work with clusters of manufacturers for White Label Manufacturing having the following certification: WHO GMP, EU-GMP, PIC/s, UKMHRA etc.

SIDDHA PHARMACY

SIDPATEL6389@GMAIL.COM

WWW.SIDDHAPHARMA.COM
WWW.SIDDHAGLOBAL.COM
GSTIN – 24ACWFS1209B1ZB
IEC CODE – ACWFS1209B

CONTACT NO. / WHATSAPP NO. - +91-8866 86 2020

11:44,  20 Jul 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 currently export to more than 51 countries.


Kindly contact us +91 987-688-2973 or send email enquiry@healthbiotech.in


Thanks,

Health Biotech Limited
Phone : +91 987 688 2973
Email : enquiry@healthbiotech.in
Website : www.healthbiotech.in

17:50,  20 Jul 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

07:09,  24 Jul 2022
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