01 Mar 2024

Reply

Pipotiazine Palmitate (12 kg) API needed in Ecuador [ENA19121]
A company that focuses on distribution & manufacturing of various pharmaceutical products is looking for suppliers of Pipotiazine Palmitate (12 kg) API for commercial purposes. The suppliers must support this enquiry with DMF, GMP & CoA.

Comments :

gauravkumar4368@gmail.com

Dear Sir / Madam,

We can offer APIs along with the supporting documents.Kindly let us know your email id so that we can send you the email and we can give you the best price.

Best Regards,
Gaurav Kumar
gauravkumar4368@gmail.com
Indo Pharm
INDIA

15:21,  01 Mar 2024

info@crystalchemicals.ae

Crystal Chemicals FZ LLC is an Importer, Exporter & Distributor of Active Pharmaceutical Ingredients (API’s) in Dubai, United Arab Emirates (UAE)

We can supply the following API, please contact

CRYSTAL CHEMICALS FZ-LLC
(Pharmaceuticals API's Distribution House in UAE)
Mobile & (Whatsapp) +971542360830
www.crystalchemicals.ae
info@crystalchemicals.ae, crystalchemicalsfzllc@gmail.com,

18:56,  05 Mar 2024

Cristonelifecare@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

23:31,  05 Mar 2024

sam.d@micoson.com

we are Micoson Biopharm Co,.Ltd company from China. We will provide quotation and document support, please send an email to sam.d@micoson.com, we will reply in time. Thank you.

19:47,  14 Mar 2024

contact@clearsynthlabs.com

Reply: Pipotiazine Palmitate API
Clearsynth Labs is Manufacture/Wholesale Supplier of WHO cGMP, ISO, and GMP quality APIs, Intermediates, Excipients… with CoA, Chemical research… and services from India, UAE, Europe, Canada, US that meet customer and regulatory requirements (USDMF/CEP) compliance at a competitive price. Kindly contact us for your requirement.

Regards
17, Lotus Business Park
Andheri West
Mumbai - 400 053
Maharashtra State
Tel/WhatsApp: +91-8074411410
contact@clearsynthlabs.com

05:46,  02 May 2024
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