13 Feb 2023

Reply

Tender// Various Finished Dosage Formulations needed in Bulgaria [ENA16360]
Specialized Hospital For Active Treatment Of Hematological Diseases Ead is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 22-Feb-2023.
1. Venetoclax (100 mg) Tablets. The required quantity is 17,000,000 units.
2. Midostaurin (25 mg) Capsules. The required quantity is 300,000 units.

Comments :

chowdary@carbontree.in

Dear Sir,

We have exclusive Oncology FDF manufacturing facility with WHOGMP/EUGMP and producing more than 200 products. Most of the products available eCTD dossiers

1. Venetoclax (100 mg) Tablets. The required quantity is 17,000,000 units.
Lead time. 4-5weeks

2. Midostaurin (25 mg) Capsules. The required quantity is 300,000 units.
NA

Please send your enquiry along with required documents.

Regards
PA Chowdary
arunodayalabs@gmail.com
bd@spaccurelabs.com
www.spaccurelabs.com
EUGMP, Korean GMP, WHOGMP, PICs approvals, Belarus, Mexico, UKMHRA approved facility

11:44,  13 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

21:16,  13 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

14:32,  22 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

14:34,  22 Feb 2023
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