Reply
infocnpharma@gmail.com
please contact on 9896446440 or infocnpharma@gmail.com
venkataskodi@gmail.com
Hi Sir/Madam
We are from RangSubbs Pharms(India) PVT Ltd, and interested in your Inquiry, We request you kindly provide a detailed inquiry. We are capable of providing requested API as per your requirement.
Thanks with best regards
Venkata S Kodi
venkataskodi@gmail.com
RangSubbs Pharma(India) PVT Ltd
Hyderabad, India
effepi@effepipharm.it
Dear Sir,
we can supply Nystatin usp/ep
Regards
effepi@effepipharm.it
luisa.goglia@fischer-group.ch
Please contact Fischer Chemicals AG
Thank you
heliantus@heliantus-milano.it
Hi,
We are Heliantus SRL, a global supplier of APIs and excipients, based in Milan, Italy.
We noticed your interest in this product and would be glad to offer our support as a trusted and efficient sourcing partner.
Feel free to contact us at heliantus@heliantus-milano.it or call us directly at +39 329 205 8269.
We look forward to hearing from you!
Best regards,
The Heliantus Team
Cristonelifecare@gmail.com
Cristone Life Care is globally connected, offering efficient quality products from EU-GMP, UK-MHRA, USFDA, PICS, and WHO-GMP approved facilities as follows:
* Pharmaceutical and Biosimilar APIs, and finished formulations.
* Oncology Exclusivity
* Antibody Drug Conjugates.
* Nutraceutical/Food Suppliments
* Critical Care and Life Savings drugs.
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* Vaccines
For export orders,
connect with us at www.cristoneglobal.com. Send your inquiries to cristonelifecare@gmail.com; marketing@cristoneglobal.com. #Pharmaceuticals #Biosimilars #ExportOrders
hostrinlifesciences@gmail.com
Hostrin Life Sciences
*One Stop For Pharmaceutical and Biosimilar Regulatory Solutions.
Hostrin offers the following services:
1.Out-licensing Dossiers
2.Dossiers in CTD/ACTD/eCTD formats
3.CDMO (Contract Research & Development)
4.Tech transfer support and Registration of Dossiers in all markets.
5.eCTD publishing with potential softwares and addressing post submission queries from all regulatory authorities.
6.Computer System Validations (CSV) as per GAMP 5 Guidelines, PLC/SCADA/HMI Validation and Documentation.
7.BE studies and clinical studies from US-FDA, EU-GMP, UK-MHRA, TGA-Australia/GCC/ANVISA approved CRO's/BE Study Centers.
8.Synthetic Resin technologies support.
9.Cleaning validation/ toxicology study reports (PDE/ADE I OEL) values for API's & FDF's
10.Pharmacovigilance
11.QBD & QMS_Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP Assessment Audits
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
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WhatsApp: +91 9949930343
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