21 Oct 2025

Reply

Adenosine API needed in Japan [ENA24359]
A company that focuses on the development and manufacturing of various pharmaceutical products is looking for suppliers of Adenosine API for development purposes. The suppliers must support this enquiry with CoA.

Comments :

bd@saimanchemsynth.com

Dear Business Team:
Please contact us for this product at bd@saimanchemsynth.com. Thank you.
From:
Dr. Haldar, PhD
SAIMAN ChemSynth Pvt. Ltd. India

17:57,  21 Oct 2025

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.
* Impurity's and RLD's
* Vaccines

For export orders,
connect with us at www.cristoneglobal.com. Send your inquiries to cristonelifecare@gmail.com; marketing@cristoneglobal.com. #Pharmaceuticals #Biosimilars #ExportOrders

20:53,  21 Oct 2025

bd@saimanchemsynth.com

API Supply Support – From Gram to Metric Ton Scale

Dear Business Team,

We would be pleased to support your requirements for Active Pharmaceutical Ingredients (APIs). SAIMAN ChemSynth Pvt. Ltd. can supply materials ranging from gram to metric ton scale, complete with DMF and COA documentation.

Please feel free to contact us for your specific needs.

Kind regards,
Dr. Animesh Chandra Haldar, Ph.D.
Managing Director
SAIMAN ChemSynth Pvt. Ltd.
?? Email: bd@saimanchemsynth.com
???? Website: www.saimanchemsynth.com

07:48,  22 Oct 2025

luisa.goglia@fischer-group.ch

Dear Al,

Kindly contact Fischer Chemicals AG in Switzerland.
We can help with this product.
Thank you.

12:41,  22 Oct 2025

hostrinlifesciences@gmail.com

Hostrin Life Sciences
*One Stop For Pharmaceutical and Biosimilar Regulatory Solutions.

Hostrin offers the following services:

1.In and out licensing Dossiers
2.Dossiers in CTD/ACTD/eCTD formats with e-softwares.
3.BE & Clinical studies Studies
4.CDMO (Contract Research & Development)
5.Tech transfer support and registration of dossiers in all markets.
6.Computer System Validations (CSV) as per GAMP 5 Guidelines, PLC/SCADA/HMI Validation, and Documentation.
7.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 visit our website www.hostringlobal.com

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
Mobile/
WhatsApp: +919949930343

23:10,  23 Oct 2025
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