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1. COA, MSDS copy
2. Local GMP, International GMP
3. DMF status
4. Price for R&D and Commercial, CIP AIR MEXICO
5. Product transportation temperature
6. U.S. FDA inspection history for this product
Comments :
keysales@sina.com
Please send the details to my email, and I will calculate and reply asap.
Thank you.
Mr.Key T
marketing@baschamlifesciences.com
Greetings from Bascham Life Sciences
We are pleased to inform you that we can support this requirement. Kindly share your contact details on our email to proceed further
Regards
Bascham Team, India
jgq@yangzijiang.com
hello, I am Justin from Yangtze River Pharmaceutical Group in China, we are the APIs manufacturer.
We will work on your inquiry, please send inquiry to my email
jgq@yangzijiang.com
Tel., WhatsApp and Wechat: +86 15261051195
Skype: jiaguanqun@hotmail.com
QQ: 348196586
joy@chemsphere.com.tw
Hi Madam/Sir,
Our Doxorubicin is already filed US DMF and will be inspected by US FDA soon.
Could you please let me know your customer's name and his forecast?
BR & Thank you.
shiqx@jymed.cn
shiqx@jymed.cn
Hello this is Claier from JYMed.
1.FDA approved & cGMP manufacturing facilities
2.Large production capacity with an annual production over 1,000kgs
3.Wide range of quality peptide products for different applications/Full service including CRO/CMO support.
Any peptide requests, freely contact us.
Skype:1052088961
WhatsApp:+86 13906985537
shiqx@jymed.cn
shiqx@jymed.cn
Hello this is Claier from JYMed.
1.FDA approved & cGMP manufacturing facilities
2.Large production capacity with an annual production over 1,000kgs
3.Wide range of quality peptide products for different applications/Full service including CRO/CMO support.
Any peptide requests, freely contact us.
Skype:1052088961
WhatsApp:+86 13906985537
bhushan.shah@macchemgroup.com
Hi , pls send your enq. of Cytarabine on my personal email id to proceed ahead
bhushan.shah@macchemgroup.com
Hi , pls send your enq. of Cytarabine on my personal email id to proceed ahead
hostrinlifesciences@gmail.com
Dear Friend,
Greetings from Hostrin Life sciences!!!
We have been supporting for the following services.
1.We do support DM for API's, Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/USA support in CTD, ACTD, eCTD and ANDA's formats with 5 modules including BA and BE studies /Clinical studies/trials for API's & Formulation's in Pharmaceutical, Ayurveda, Biotech, Biosimilar, vitamins , Peptides and recently Transdermal patches too.
2. Impurity's & Reference standards support for API's
3. Services for IPR & Regulatory compliance
4. 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.
5. Custom synthesis & Contract manufacturing services
6. Synthetic Resins technologies support
Pls don't hesitate to send your enquiry. 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
