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1. Micronized Progesterone (100 mg X 30) Capsules. The required quantity is 84,797 units.
2. Micronized Progesterone (200 mg X 30) Capsules. The required quantity is 144,315 units.
3. Micronized Progesterone (400 mg X 20) Capsules. The required quantity is 1,080 units.
vishvesh.shaishav@gmail.com
We are focussed on developing new manufacturing technologies, including custom synthesis of new moleculepharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, pharmaceutical pellets,additives, contract manufacturing, chemicals. We began in the field of specialty intermediates for pharmaceutical applications and developed our own purification technologies for manufacturing highly pure intermediates. And Pharmaceutical API At a later stage, we integrated forward to manufacture finished formulations for both veterinary and human consumption. Due to our completely integrated operations in the pharmaceutical sector, we continuously learn about the quality parameters for an API based on the performance of the finished formulation in order to quality their Bioequivalence Studies.?We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.?Our focus lies in developing new production technologies with a keen interest in frugal innovation in order to gain a competitive edge over others. We specialize in the custom synthesis of molecules and work with many reputed companies around the world on an OEM basis.pharmaceutical pellets,Intermidiates ?Our finished formulations from WHO-GMP and EU-GMP units are registered/being registered in 26 countries within Asia, Europe, North America, Latin America and Africa continents including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad, Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.?vishvesh.shaishav@gmail.com
+919725487108
+919726387108
info@aeqpharma.com
we can support you
tautvydas@litfarma.com
Hello,
we are Litfarma company, EU Authorized Pharmaceutical Wholesaler based in Lithuania.
We are very active in Government Tenders and Hospital Supplies and have access to proprietary and generic medicines, medical devices, supplements - all authorized, certified, approved, notified or licensed in at least one EU country.
If your request is still valid, please get in touch with me directly at tautvydas@litfarma.com.
Thank you!
Tautvydas at #Litfarma Company
Lithuania, EU
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 formats. DMF support for API's as well.
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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.
3. Support for Impurity's, Reference standards and RLD's
4. Services for IPR & Regulatory compliance with all risk assessments.
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.
7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.
8. Synthetic Resin technologies support.
9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.
10. 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
www.hostringlobal.com
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 namrata.sutphinrx@gmail.com
vp123sd@rediffmail.com
WE CAN HELP YOU WITH THE REQUIREMENTS WITH THE BEST PRICE POINT
amtechmedicine01@gmail.com
we are a mfg company in nepal with who-gmp certification.
we have more than 150 products.
haoran.tse@gmail.com
Dear sir, hiram from Chengdu Pukang here, we can supply the drugs you need, which will be delivered from China.
raonk5@gmail.com
Dear Sir,
I can support in giving best formula and process in line with US/EUROPE NDA formula and process and support in preparation dossier. Looking forward for your valuable feedback about this. Need not bother about dossiers which are more theoretical yet times.
Thanking you sir and best regards
Kamalakar Rao N
M.PHARM
INDIVIDUAL CONSULTANT-FORMULATION DEVELOPMENT, DOSSIER SUPPORT & MANUFACTURING
CAN SHARE MY RESUME ONCE RECEIVE YOUR FEED BACK
