Reply
1. Ritonavir (100 mg) Film-coated Tablets. The required quantity is 13,830 units.
2. Raltegravir (400 mg) Film-coated Tablets. The required quantity is 16,620 units.
chowdary@carbontree.in
Dear Sir
We do supply from our WHOGMP/EUGMP facility
Ritonavir (100 mg) Film-coated Tablets. The required quantity is 13,830 units.
Lead time. 3-4weeks
2. Raltegravir (400 mg) Film-coated Tablets. The required quantity is 16,620 units.
Lead time. 3-4weeks
pharmahouse@ymail.com
Services offered by PHARMA HOUSE
Dossiers (CTD, e-CTD, ANDA and ANVISA)
(All Country Specific, As per client request)
DMFs(CTD, e-CTD)(Open &Closed part)
(All Regions and Country regulations)
Technology transfers(API'S &Formulations),
( Paper technology & Product Development)
Pharmacovigilance(PV),
Intellectual properties(IP)
AMV, BMR, BPR AND BE Reports (As per country specifications)
We have seperate Teams for Product Development for API'S &Formulations.
All product Documentations
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
murali@venkatabalajilabs.com
Dear Sir/Madam,
We can provide the required finished dosage form in a state-of-the-art manufacturing facility, tailored to meet your specific needs. Our team is dedicated to delivering high-quality products that comply with international standards, ensuring timely delivery and competitive pricing. Please let us know if you have any further requirements or questions.
Best regards,
Murali.
Email: murali@venkatabalajilabs.com
