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1. Amoxicillin (500 mg) Capsules. The required quantity is 80,000 units.
2. Bromhexine (12 mg) Tablets. The required quantity is 12,000 units.
3. Carbamazepine (200 mg) Tablets. The required quantity is 12,000 units.
Comments :
sales@pelcoat.com
We are PELCOAT FORMULATION, a GMP UNIT, Hyderabad, India an integrated growing health care company started in 2007, is aiming to become one of the fastest-growing pharmaceutical export company ( 60% contributes export in our turnover) in India. Pelcoat formulations manufacture wide range of Finished Pellets Formulations (ready to fill pellets) and DC Granules. We offer more than 200 range of pellets, in India only 3 manufacturers offer this kind of range.
New products:- We can also offer specia
Krishna@hrvglobal.com
Could you please share your target markets
namrata.sutphinrx@gmail.com
Sutphin Drugs Inc are licensed distributors of USFDA approved Reference Listed Drugs (RLD’s) ,Branded & Generic & Comparator Drug Products.
Kindly contact at info@sutphinrld.com or sutphinrx@gmail.com
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
