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1. CAS 5341-49-1 Impurity
2. CAS 125-79-1 Impurity
3. CAS 6293-01-2 Impurity
4. CAS 5341-49-1 Impurity
5. CAS 86-29-3 Impurity
Comments :
aksu_zhyr@163.com
We have a lot of impurities and look forward to further communication
aksu_zhyr@163.com
We have a lot of impurities and look forward to further communication
sales@clearsynthlab.com
Reply: Methadone Impurities
Clearsynth demonstrates the ability to consistently provide products 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.
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Mr. V. Ambati
International Sales & Business Development
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
+91-9394436878
sales@clearsynthlab.com
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
Dear Sir,
Greeting from Kantam research,
With reference to your recent enquiry on
1. CAS 5341-49-1 Impurity-custom synthesis-3 to 4 weeks
2. CAS 125-79-1 Impurity--ready stock
3. CAS 6293-01-2 Impurity-ready stock
4. CAS 5341-49-1 Impurity-same as above
5. CAS 86-29-3 Impurity is readily available in stock. Kindly confirm the same and give us opportunity to serve you mean while please share email id so that we will able to share our COA and other data's.my mail id kantamrch@gmail.com,
marketing@endofar.com
Dear Friend
We believe that we can fulfill your requirements.
Please contact us on following details.
E-mail: Marketing@Endofar.com
I’m waiting for your kind email.
ENDOFAR Ilac Co. is a pharmaceutical company in Istanbul, Turkey. Our portfolio contains several specific #APIs & #Finished Dosage form medications in the field of Natural #Cannabinoid & #Opioid medications, #Cosmeceuticals & also #Nutraceutical Supplements.
SPECIAL OFFER from ENDOFAR ?laç
1. API Supply
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5. Providing CTD/ FORMULLA for FDFs
6. European Out-Licensing
You can also find our product list here:
*** https://drive.google.com/file/d/1n34VPTXgPcdpeTA-yuG3uBY-5W2N1n7S/view?usp=share_link***
