Market Place
Reply
1. Omeprazole (20 mg) Capsules. The required quantity is 110,620 units.
2. Drotaverine (80 mg) Tablets. The required quantity is 59,870 units.
Comments :
chowdary@carbontree.in
Dear Sir,
We do supply both from our WHOGMP, EUGMP facility in 3-4weeks
1. Omeprazole (20 mg) Capsules. The required quantity is 110,620 units.
2. Drotaverine (80 mg) Tablets. The required quantity is 59,870 units.
srcglbl@gmail.com
Kindly send us your requirements on srcglbl@gmail.com
export_commercial@bdpasargad.com
Dear Sir or Madam
We are excited to introduce to you, our company .
I’m writing to introduce our company BD Pasargad ,trading company in the field of finished dosage
We are currently exporting medicine to many countries.
We can prepare pharmaceutical products (tablet , capsule , ampule , prefilled syringe ,… ) in best price , we can support GMP , DMF or CTD for Registration .
Thanks, and best regards
Mohamad Norouzi
BD Pasargad
Mob : +989397665038
export_commercial@bdpasargad.com
Dear Sir or Madam
We are excited to introduce to you, our company .
I’m writing to introduce our company BD Pasargad ,trading company in the field of finished dosage
We are currently exporting medicine to many countries.
We can prepare pharmaceutical products (tablet , capsule , ampule , prefilled syringe ,… ) in best price , we can support GMP , DMF or CTD for Registration .
Thanks, and best regards
Mohamad Norouzi
BD Pasargad
Mob : +989397665038
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
