28 Jun 2022

Reply

Various Excipients needed in Italy [ENA14118]
A pharmaceutical company that focuses on the development and manufacturing of various finished dosage formulations is looking for suppliers of Various Excipients for commercial purpose. The suppliers must support this enquiry with GMP & CoA.
1. Sucrose RFS (13 MT/ annum) Excipient
2. Tartaric Acid (2.2 MT/ annum) Excipient
3. Essence of Lemon (3 kg/ annum) Excipient
4. Essence of Raspberry (3 kg/ annum) Excipient

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
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVE

11:32,  28 Jun 2022

SALVAVIDAS PHARMACEUTICAL PVT.LTD

We are A Reputed Pharmaceutical Product manufacturer, Exporter, and Export of various types of Pharmaceutical Products throughout the world.

We are dealing in Active Pharmaceutical Ingredients (API’s), Veterinary APIs, Intermediates, Excipients & Chemicals… We deal with Branded Drugs along with all Related Documents and Certificates.

We have a wide range of Medicines like Antibiotics, Cardio diabetics, Anti-Cancer, Nutraceuticals & Many more.

We are always there to serve you with our best services

All Products are Manufactured in WHO, GMP, ISO 9001 certified manufacturing units.

Best Regard.
Rohan Patel
Business Development Executive
Email- rohan@salvavidaspharma.com
Whatsaap- +91-9313237877
Web: www.salvavidaspharmaceutical.com

13:54,  28 Jun 2022

kps@knowellpharma.com

We have ready stock of the mentioned excipients . We Supply the GMP certificate along. with the COA .

22:42,  28 Jun 2022

kps@knowellpharma.com

We have ready stock of the mentioned excipients . We Supply the GMP certificate along. with the COA .

22:42,  28 Jun 2022

srcglbl@gmail.com

Contact us for best offer

22:46,  28 Jun 2022

a.izadi@pharmanova.ae

Dear Sir/Madam,

I hope everything is well on your side.

PharmaNova is a wholesaler pharmaceutical raw material company and located in Dubai UAE with branches in Turkey, India and Hong Kong. We are providing top quality pharmaceutical raw material worldwide. We have very good network within China, India and Europe to support our customers worldwide from certified and regulated API and Excipients manufacturers, audited by international MOHs.

We are able to support you with this inquiry from certified source.

Best regards,

Ashkan Izadi
Business Development Specialist
Cell: +971 52350 0672
Tel: +971 4 409 6859
FAX: +971 4 409 6850
www.pharmanova.ae

11:32,  29 Jun 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

23:07,  29 Jun 2022

muming@gemincare.com

API manufacturing, customized synthesis, CDMO services please contact email or whatsapp: +8615240249432

07:10,  02 Jul 2022

heliantus@heliantus-milano.it

Buonasera

Abbiamo Tartaric Acid a magazzino. Se vi serve contattateci a:

heliantus@heliantus-milano.it

Un saluto

Marco

00:16,  16 Jul 2022
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