Reply
sales@neochempharma.com
We can supply Cyanocobalamin please contact us for your requirement of API & EXICIPIENTS.
Dr Madhavi patel
Email : sales@neochempharma.com
Mobile : +91 8320528643
dimasromi@yangzijiang.com
We are able to supply this product. Please feel free to contact us for your API and excipient requirements from China.
Dimas Romi
Email: dimasromi@yangzijiang.com
Mobile: +86 18602523687
sibi.gopalsamy@nhgpharma.com
We New Horizon Pharma are Manufacturers of APIs, supplying to global regulatory markets, including the US, EU, LATAM & MENA. With strategic sales offices in 7 locations worldwide, we supply niche and orphan drug APIs,We are equipped with a diversified portfolio of APIs with USDMFs & CEPs manufactured in USFDA/EU GMP compliant facilities. In addition to this, we represent 7 Indian Partner Sites with their portfolio of over 400 APIs.
marketing@hengkangpharm.cn
Zhejiang Hengkang group is FDA, EUGMP, PMDA, ANVISA, MFDS, NMPA approved company. Specialized on manufacturing & supplying various intermediates, APIs, FDFs with high quality and documentaiton.
bhargavshubham7017@gmail.com
bhargavshubham7017@gmail.com
Hello
I can help you connect with verified suppliers of API and Excipient for commercial use. I work with suppliers who can provide CoA and standard specifications, and can assist in negotiating the best terms.
If you are interested, I can share details and help you arrange a smooth transaction.
Contact: [Shubham/ bhargavshubham7017@gmail.com/ 7017059928]
Looking forward to assisting you.
Best regards,
[Shubham
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
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
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
