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1. USP Grade Cyclopentolate Hydrochloride API. The required quantity is 200 g in 3 lots and 500 g/ month or 2 months.
2. Sodium Nitrite API. The required quantity is 50 kg.
Crystalchemicalsfzllc@gmail.com
Dear Friend,
Please contact on the following emails for quotation.
Thanks and Regards,
Dr. Amna Nawaz
CRYSTAL CHEMICALS FZ-LLC - UAE -|- China -|- Pakistan
M: +92-321-8444610 (Whatsapp)
Skype: Crystalchemicals786
E: import@crystalchemicals.com.pk, Crystalchemicalsfzllc@gmail.com
W: www.crystalchemicals.com.pk
alicechan@huarizy.com
HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.
1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80
email address: alicechan@huarizy.com
phone number: +86 18820220687
himali.pawaskar@dksh.com
Hi, Please share this lead
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
snamarketing1@gmail.com
we are WHO GMP, Indian GMP and ISO certified factory for this product. Kindly email us at snamarketing1 @ gmail . com
snamarketing1@gmail.com
we are WHO GMP, Indian GMP and ISO certified factory for this product. Kindly email us at snamarketing1 @ gmail . com
snamarketing1@gmail.com
Hello,
We are WHO - GMP, Indian GMP and ISO certified manufacturer of API, Intermediates and Excipients.
We can offer Cyclopentolate Hcl IP / BP / USP / EP with DMF, GMP, WHO-GMP
Please email on snamarketing1@gmail.com
