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vishvesh.shaishav@gmail.com
We are a one of the leading Indian manufacturer, supplier, importer, dealer, distributor, trader, exporter that is used in pharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, additives, contract manufacturing, chemical compound for pharmaceutical and chemicals process industry available at best price
We are exporting several of our products to Latin American countries, Gulf & Asian countries and also a few products to Australia, UK & USA.
Regulatory documents service etc.
Vishvesh.shaishav@gmail.com
vishvesh.shaishav@gmail.com
We are a one of the leading Indian manufacturer, supplier, importer, dealer, distributor, trader, exporter that is used in pharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, additives, contract manufacturing, chemical compound for pharmaceutical and chemicals process industry available at best price
We are exporting several of our products to Latin American countries, Gulf & Asian countries and also a few products to Australia, UK & USA.
Regulatory documents service etc.
Vishvesh.shaishav@gmail.com
c.papadi@famar-group.com
Please let me know how can we support you. FAMAR has 6 GMP approved sites, including 3 solids sites.
anu.p@umedicalabs.com
We are a EU-GMP Certified Manufacturer for Oral Solids and would be interested in collaborating with you for Manufacture of Omeprazole Capsules.
Would need some additional information to be able to take our discussion forward.
My contact details are as Follows;
Anu Pariyarath
anu.p@umedicalabs.com
hostrinlifesciences@gmail.com
Dear Friend,
Greetings from Hostrin Life sciences!!!
We have been supporting the following services.
1.We do support DMF for API, Tech transfer support and Registration of Dossiers in ROW/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 & Formulations 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 & Contract manufacturing services
6. Synthetic Resins technologies support
Pls don't hesitate to send your enquiry's. 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
monica.oneglio@adarepharma.com
We are a specialty CDMO with experience in fluid bed Wuerster coating and capsules filling with humidity control. Our GMP facility in Italy is FDA EU and Japanese approved and has completed successful tech transfer under the lock down conditions. We would like to enter into a CDA to receive a detailed RFP.
Thank you and best regards
j.raina@aconitum.lt
we Aconitum uab based in Lithuania having EU GMP. CAN do the need full.
philippe.tschopp@glatt.com
Glatt Pharmaceutical Services has to GMP sites with a strong expertise on multiparticulates / pellets. Interested to hear more.
hoventapharma@gmail.com
Dear sir/madam,
We would like to take this opportunity to introduce Hoventa Pharma,
We offer various kinds of services in addition to supplies of APIs,and intermediate, we undertake long-term contracts for manufacturing intermediates and development of new Active Pharmaceutical Ingredients as per your requirement
hoventapharma@gmail.com
Dear sir/madam,
We would like to take this opportunity to introduce Hoventa Pharma,
We offer various kinds of services in addition to supplies of APIs,and intermediate, we undertake long-term contracts for manufacturing intermediates and development of new Active Pharmaceutical Ingredients as per your requirement
leo.su@phc-pharm.com
Hi Sir,
We have serval CDMO partners are suitable for your project. We would like to send you the candidate's capability for your reference. Kindly let us know your mail address for further discussion. Thanks.
We PHC pharmaceutical, a CDMO agency service provider base in Taiwan. If you are looking for the alternative supplier or CRO/CDMO for your project. We are able to support you to find a suitable CDMO/CRO partners. Enclosed please find our company presentation for your reference. Please feel free to contact us if you have any questions. Thanks. PHC establishes a stable partnership with several CDMO companies specializing in CDMO service of API (cytotoxic /general), FDF (oral & Injectable), sterile APIs and biologicals. Our team has developed and transferred multiple ANDA/NDA projects for US and EU during the past few years and we are fully aware of the keys to deliver our client’s project successfully. Our team members are specialized and experienced in the areas of project management, manufacturing, regulatory affair, and quality in pharmaceutical industry.
Warm regards, Leo Su
Leo Su
General Manager at PHC pharmaceutical
A No. 259, Zhenqian St., Shulin Dist., New Taipei City 238, Taiwan.
T +886 286860242
M +886 928560046
E leo.su@phc-pharm.com
W www.phc-pharm.com
jgq@yangzijiang.com
jgq@yangzijiang.com
I am Justin from Yangtze River Pharmaceutical Group in China
APIs and FDF can be manufactured by our company.
We can also CMO
If you need them, please contact me by Tel., WhatsApp and Wechat: +86 15261051195
Email: jgq@yangzijiang.com
export@healthpharma.in
Dear Sir,
Greetings from Health Pharma...!!!
We can support you with your requirements. Kindly request you to send email for detailed information.
Looking forward to your positive response.
Thanks...!!!
