23 Apr 2022

Reply

Cyclophosphamide API needed in the United States [ENA13414]
A company that provides consultancy services to pharmaceutical industry is looking for suppliers of Cyclophosphamide API. The required quantity is 10 kg for development & 200 kg - 1 MT/ annum for commercial purpose. The suppliers must support this enquiry with USDMF.

Comments :

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

15:27,  23 Apr 2022

arunodayalabs@gmail.com

Dear Sir
We supply Cyclophosphamide API from USFDA facility

16:24,  23 Apr 2022

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

17:16,  23 Apr 2022

pharmahouse@ymail.com

Services offered by PHARMA HOUSE

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,
What's App & Voice:+91 81433 69525
pharmahouse@ymail.com ,
Hyderabad, India

11:03,  24 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

06:23,  25 Apr 2022

marketing.neion@gmail.com

We offer sterile grade from USFDA approved plant

13:53,  25 Apr 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

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

21:42,  25 Apr 2022

api@caren.se

Please send your full regulatory requirements to our email.
Our international team will be able to look into this for you.


Best Regards,
Ming Yuzhen (Marketing & Sales)

Tel: +8618411631209
Email: api@caren.se

01:46,  27 Apr 2022

kindly share with us inquiry by email please

10:27,  27 Apr 2022

himali.pawaskar@dksh.com

Hi , Share this lead

10:48,  27 Apr 2022
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty