07 Feb 2023

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Tender// Various Finished Dosage Formulations needed in Estonia [ENA16318]
Foundation Tartu University Clinic is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 7-Mar-2023.
1. Potassium Chloride (600 mg) Extended-Release Capsules. The required quantity is 200,000 units.
2. Calcium Gluconate (100 mg/ ml in 10 ml) Injections. The required quantity is 60,000 units.

Comments :

srcglbl@gmail.com

Kindly send us your requirements on srcglbl@gmail.com

11:34,  07 Feb 2023

pharmahouse@ymail.com

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)
We have seperate Teams for Product Development for API'S &Formulations.
All product Documentations (Process, training, trouble shooting)
&other Regulatory services
Pharma House,
+91 8143369525

19:11,  07 Feb 2023

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

21:38,  07 Feb 2023

hoventapharma@gmail.com

Dear sir/madam,

We would like to take this opportunity to Introduce Hoventa Pharma,
We offer various kinds of services in addition to supplies of APIs,and intermediate, we undertake long-term contracts for manufacturing intermediates and development of new Active Pharmaceutical Ingredients as per your requirement

14:46,  22 Feb 2023
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