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damian.webb@activepharma.co.uk
Good afternoon
we can supply this product and have qty available
I would like to introduce Active Pharma Supplies Ltd. to your company.
We are a UK-based provider of top-quality API’s, excipients, intermediates and fine chemicals. From our base in Lancashire, Northwest of England we source, procure, store and supply products to support your regulatory requirements
Marketing.endo@pluviaglobal.com
Dear Friend
We believe that we can fulfill your requirements.
Please contact us on following details.
E-mail: Marketing.endo@pluviaglobal.com
Website: https://pluviaendo.com/
Our products: https://bit.ly/3TVnpoS
I’m waiting for your kind email.
snamarketing1@gmail.com
Hello,
We are WHO - GMP, Indian GMP and ISO certified manufacturer of API, Intermediates and Excipients.
Please email on snamarketing1@gmail.com
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 formats. DMF support for API's as well.
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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.
3. Support for Impurity's, Reference standards and RLD's
4. Services for IPR & Regulatory compliance with all risk assessments.
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.
7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.
8. Synthetic Resin technologies support.
9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.
10. 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
www.hostringlobal.com
gauravkumar4368@gmail.com
Dear Sir / Madam,
We can offer Erythromycin API along 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
a.sharma@bazayan.ch
Dear Sir,
Please share more details of your requirement with EP grade and documentary support needed ASMF/DMF?
ajapharma21@gmail.com
Dear Sir,
We are one of the leading Pharmaceutical API Exporter from India. We will supply APIs including Erythromycin from the WHO GMP approved Plants.
Kindly send us more details on ajapharma21@gmail.com
ajapharma21@gmail.com
Dear Sir,
We are one of the leading Pharmaceutical API Exporter from India. We will supply APIs including Erythormycin from the GMP / WHO GMP approved Plants.
Kindly send us more details on ajapharma21@gmail.com
Mrs. Amutha Selvakumar
A.J.A. Pharmachem
101/3, Sarvodaya Galaxy,
Koper Road,
Dombivali (W), Dist. Thane
Pin : 421202 - India
Tel.No. : 91-251-2460292
Mobile : +919819187260
e-mail: ajapharma@gmail.com / ajapharma21@gmail.com
himali.pawaskar@dksh.com
Hi ,Please share this lead
sales@mishupharma.com
Dear Sir/ Madam,
We are a supplier based in India. We have experience of supplying pharmaceutical products for more than 13 years. Please let us know if we can provide you with solution.
You can visit our website www.mishupharma.in.
Regards
Mahima
bd1@mehtaapi.com
Mehta API, a 55-year-old manufacturing company with EU GMP, PMDA, and WHO-GMP approvals. We specialize in the production of APIs and intermediates. Currently, we export our APIs to over 40 countries, holding active DMF registrations or filings in key markets such as the EU, China, Japan, Russia, Turkey, and more. We wish to offer you Micronized Erythromycin. Please send an email at bd1@mehtaapi.com and we will send you all the supporting documents.
bd1@mehtaapi.com
Mehta API, a 55-year-old manufacturing company with EU GMP, PMDA, and WHO-GMP approvals. We specialize in the production of APIs and intermediates. Currently, we export our APIs to over 40 countries, holding active DMF registrations or filings in key markets such as the EU, China, Japan, Russia, Turkey, and more.
We wish to offer you Micronised erythromycin. Please send an email at bd1@mehtaapi.com and we will send you all the supporting documents.
