21 Dec 2022

Reply

Injectable Grade Methylergometrine (MOQ) API needed in India [ENA15876]
A company that deals in various pharmaceutical products like injections, syrups & hygiene products is looking for suppliers of Injectable Grade Methylergometrine (MOQ) API for commercial purposes. The suppliers must support this enquiry with CoA.

Comments :

bdevomaar@gmail.com

Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
Kind regards

14:29,  21 Dec 2022

info@eqpharma.com

METHYL ERGOMETRINE MALEATE USP/IP API with full support docs

20:56,  21 Dec 2022

sales@clearsynthlab.com

Reply: Injectable Grade Methylergometrine API

Clearsynth demonstrates the ability to consistently manufacture APIs, Intermediates, Chemical research… and services that meet customer and regulatory requirements. Kindly confirm your requirement by email so we can provide the Quotation, COA...

Regards

Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
www.clearsynthlab.com
Tel/WhatsApp: +91-9394436878
sales@clearsynthlab.com

05:03,  23 Dec 2022

hostrinlifesciences@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. 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.

3. Support for Impurity's, Reference standards and RLD's

4. Services for IPR & Regulatory compliance

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.

6. Custom synthesis and contract manufacturing services

7. Synthetic Resins technologies support.

8. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) 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

08:50,  23 Dec 2022
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