13 Oct 2022

Reply

Pharma Grade Mannitol (8 MT) Excipient needed in France [ENA15300]
European CDMO specialized in the contract development and manufacturing of pharmaceutical products for humans, animals and medical devices is looking for suppliers of Pharma Grade Mannitol (8 MT) Excipient for commercial purposes. The suppliers must support this enquiry with CoA.

Comments :

anji@globalpharmatek.com

We can supply

15:11,  13 Oct 2022

gauravkumar4368@gmail.com

Dear Sir / Madam,

We can offer Mannitol API with the supporting documents.Kindly let us know your email id so that we can send you the email and we can give you the best price.

Best Regards,
Gaurav Kumar
gauravkumar4368@gmail.com
Indo Pharm
INDIA

16:38,  13 Oct 2022

smit@salvavidaspharma.com

Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers of pharmaceutical products.
can we connect for some business?

Please, contact
smit@salvavidaspharma.com
Mo: +91 74359 19702 (Whatsapp : https://wa.link/8hjiee )
(Telegram : https://t.me/smit_slavavidas )

17:44,  13 Oct 2022

hostrinlifesciences@gmail.com

Dear friend,

Greetings from Hostrin Life Sciences!!!

We have been supporting 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 and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.

3. Impurity's & Reference standards support for API's

4. Services for IPR & Regulatory compliance

5. Services for QMS & supporting of QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars companies who are willing to enter into the Regulatory market which is mandatory to show for FDA.

6. Custom synthesis and contract manufacturing services

7. Synthetic Resins technologies support.

8. Cleaning validation/ toxicology studies reports (PD 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

00:54,  14 Oct 2022

sales@clearsynthlab.com

Reply: Pharma Grade Mannitol Excipient

Clearsynth demonstrates the ability to consistently manufacture APIs, Intermediates, Chemical research… and services that meet customer and regulatory requirements. Kindly confirm your requirement by email so we can provide the Quotation, COA within 24hrs Max from the inquiry date.

Regards

Mr. V. Ambati
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
Tel/WhatsApp: +91-9394436878
sales@clearsynthlab.com

14:41,  14 Oct 2022

enquiries@bergscp.com

Please contact us for the price.

18:35,  18 Oct 2022

himali.pawakar@dksh.com

Hi , Please share this lead

09:17,  19 Oct 2022

kaushal@newedgeoverseas.com

Please connect

11:18,  13 Jan 2023
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