02 Sep 2022

Reply

Methandienone API needed in Georgia [ENA14892]
A company that deals in various pharmaceutical products is looking for suppliers of Methandienone (MOQ) API for commercial purpose. The suppliers must support this enquiry with GMP & CoA.

Comments :

bdevomaar@gmail.com

Dear Sir,
Please send the inquiry on below email.
We can support your requierment for the API with all documents
bdevomaar@gmail.com
Kind regards

12:33,  02 Sep 2022

crystalchemicalsfzllc@gmail.com

We can supply the following API, Please contact

Crystal Chemicals FZ-LLC
(Pharmaceuticals API's Distributor in UAE)
FDRK-3517, PO Box # 10055, Ras-AL-Khaimah, United Arab Emirates
(Whatsapp) +92-333-8484130
crystalchemicalsfzllc@gmail.com
www.crystalchemicals.com.pk

13:33,  02 Sep 2022

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

14:16,  02 Sep 2022

sales@clearsynthlab.com

Reply: Methandienone API

Clearsynth demonstrates the ability to consistently provide products 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
International Sales & Business Development
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
+91-9394436878
sales@clearsynthlab.com

18:31,  02 Sep 2022

Dear Sir / Madam,

We can offer Captioned API. Can you pelase share your email id so that we can send us COA, price and other terms.

Thanks & Regards,
Mishu

16:34,  03 Sep 2022

sam.d@micoson.com

we will provide quotations and documents immediately. Please send email to sam.d@micoson.com. Thank you.

20:10,  03 Sep 2022

smit@salvavidaspharma.com

Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers and it can be available with us.
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 )

14:28,  10 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

01:57,  11 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

01:57,  11 Sep 2022

shplexim@sohanhealthcare.com

Greeting from Sohan Healthcare..The facility is audited and approved by European Authority, Russian Authority, Korea MFDS. Our facility is also USFDA complied. We hold CEP for Metformin HCl API. SHPL exports products to more than 30 countries and has more than 100 satisfied customers.
Our product details as per below
Metformin HCL EP/BP/IP/USP/CEP
Metformin DC Granules 86.66% / 93.60% / 95% / 90% / 83.33%.
Gliclazide EP/BP/IP/CEP
Folic Acid- IP, USP
Thanks
Ramnath

13:31,  24 Sep 2022
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