19 Apr 2022

Reply

Carvedilol ER (20%) Pellets needed in Pakistan [ENA13361]
A pharmaceutical company that specializes in the manufacturing of various finished formulations is looking for suppliers of Carvedilol ER (20%) Pellets for commercial purpose. The required quantity is MOQ. The suppliers must support this enquiry with CoA.

Comments :

gauravkumar4368@gmail.com

Dear Sir / Madam,

We can offer all APIs. 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
New Delhi, INDIA

11:43,  19 Apr 2022

Crystalchemicalsfzllc@gmail.com

Dear Friend,

Please contact on the following emails for quotation.

Thanks and Regards,

Dr. Amna Nawaz
CRYSTAL CHEMICALS FZ-LLC - UAE -|- China -|- Pakistan
M: +92-321-8444610 (Whatsapp)
Skype: Crystalchemicals786
E: import@crystalchemicals.com.pk, Crystalchemicalsfzllc@gmail.com
W: www.crystalchemicals.com.pk

16:04,  19 Apr 2022

INQUIRY@APIHKP.COM

Hi
We have brand new WHO GMP API manufacturing facility with FDAI LICENCE.

PL. VISIT OUR WEBSITE: APIHKP.COM

10:42,  20 Apr 2022

alicechan@huarizy.com

HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.

1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80

email address: alicechan@huarizy.com
phone number: +86 18820220687

12:08,  21 Apr 2022

hostrinlifesciences@gmail.com

Dear friend,

Greetings from Hostrin Life Sciences!!!

We have been supporting the following services.

1.We do support DMF's for API's, Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/USA support in CTD, ACTD, eCTD and ANDA's formats with 5 modules including BA and BE studies /Clinical studies/trials for API's & Formulation's in Pharmaceutical, Ayurveda, Biotech, Biosimilar, vitamins , Peptides and recently Transdermal patches too.

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

3. Services for IPR & Regulatory compliance

4. 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.

5. Custom synthesis and contract manufacturing services

6. Synthetic Resins technologies support.

7. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.

8. Pharmacovigilance services.

Pls don't hesitate to send your inquiries. For your reference, please go through our website www.hostringlobal.com

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343

23:58,  21 Apr 2022
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