Reply
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
chowdary@carbontree.in
Dear Sir,
We are producing Tramadol hcl from our GMP facility. We have all narcotic approvals and NOC
info@aeqpharma.com
Tramadol API is our mainly products.
Large quantity support with full docs.
mkp2723@outlook.com
Please mail me, I have good Source
sales@clearsynthlab.com
Reply: Tramadol 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
clearsynthlab.com
+91-9394436878
sales@clearsynthlab.com
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 )
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
lijiajing@sinobrightpharma.com
Hello~ This is Chenny, I studied Arabic in Yunnan Normal University, and after graduation I worked in medicine. Now, I'm a Sales clerk from Sinobright Pharma, an APIs supplier in China for more than 18 years.
Our partner is one of biggest manufactures which can ensure good quality and stable supplying at good price , we support with full documentaries GMP/CEP/LOA for registration.
Tel: +0086 755 86180219-8210
Mobile / WeChat/whatsapp: +86 18213475020
Mail: lijiajing@sinobrightpharma.com
crystalchemicalsfzllc@gmail.com
We are leading Exporter of TRAMADOL HCL USP API with USDMF & FDA Approved Plant. please contact
CRYSTAL CHEMICALS FZ-LLC
(Pharmaceuticals API's Distribution House in UAE)
Mobile & (Whatsapp) +971542360830
Email: crystalchemicalsfzllc@gmail.com
Website: www.crystalchemicals.ae
