21 Oct 2019

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Looking for a CMO/CDMO to develop Myo-Inositol [ENA05513]
A pharmaceutical company specialised in development of anticancer drugs, biomarkers & supplements is looking for a CMO/CDMO to develop Myo-Inositol (injectable grade) raw material. The clinical trials for the formulations will be conducted in the United States. Initial requirement would be several kilograms & will increase as clinical trials progresses. The CDMO/CMO facilities should be cGMP compliant.

Comments :

hostrinlifesciences@gmail.com

Dear Friend,

Greetings from Hostrin Life sciences!!!

We have been supporting for 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 & 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  

20:42,  22 Oct 2019

n.martinez@vnanocdmo.com

Dear,
V-nano is a new CDMO for sterile injectables in GMP conditions. We are based in south of France in Toulouse, and is more than a simple manufacturing platform for your clinical and commercial product. It is an integral part of the VBi Therapeutics group, a powerhouse for innovative approaches to pharmaceutical development providing you with a one-stop-shop for your entire supply chain.

Within one single “shop” for contract development and manufacturing, V-Nano supports all your needs for formulation, supply, manufacturing, regulatory filing and registration. For your next generation molecule market entry, you have direct access to a broad spectrum of are best-in-class services.

V-nano is a CDMO dedicated for sterile injectables and parenterals. Our aim is to support our clients from nanoformulation to fill and finish through our GMP manufacturing platform supplying quantities up to 60 liters and our cutting-edge filling line fully automated.
V-Nano manages the complete development of a wide range of active pharmaceutical ingredients (API):
• Cytotoxic or high potency API
• Conventional API
• Large molecules (included ADC)
• Small molecules

I invite you to visit our website http://vnanocdmo.com

I also stay available to answer your questions and to have more specific discussion.

Have a nice day

Best regards,

20:26,  16 Jan 2020

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...!!!

14:26,  30 Mar 2020

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

12:42,  24 Nov 2020

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

05:50,  02 Dec 2020
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