02 Sep 2022

Reply

Various APIs needed in Pakistan [ENA14886]
A pharmaceutical company that focuses on the manufacturing of various finished formulations is looking for suppliers of Various APIs for development purpose. The suppliers must support this enquiry with CoA.
1. Atogepant API
2. Difamilast API
3. Estetrol API
4. Bazedoxifene API
5. Segesterone Acetate API

Comments :

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

13:32,  02 Sep 2022

sales@clearsynthlab.com

Reply:
1. Atogepant API
2. Difamilast API
3. Estetrol API
4. Bazedoxifene API
5. Segesterone Acetate API

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

17:35,  02 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

02:09,  11 Sep 2022
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