01 Sep 2022

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Looking for an EU or WHO-GMP certified CMO to Manufacture OSDs [ENA14877]
A Turkish-based company that focuses on manufacturing a wide range of finished dosage forms in the field of natural cannabinoids, opioid medications, cosmeceuticals & nutraceuticals is looking for an EU GMP or WHO GMP certified CMO to manufacture OSDs using controlled substances or opioid APIs. The required dosage form is tablets, capsules & syrups. The geographical preference for CMO is Europe & India.

Comments :

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

11:13,  01 Sep 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
Whatsapp +91 9033215377
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVE

14:05,  01 Sep 2022

chowdary@carbontree.in

Dear Sir,
We have exclusive Oncology FDF manufacturing facility in Hyderabad, India with EUGMP, MHRA, Korean GMP, WHOGMP and PICs approvals. Producing more than 250 products and most of the products available eCTD dossiers.

Please contact personally bd@spaccurelabs.com
www.spaccurelabs.com

15:04,  01 Sep 2022

enquiry@healthbiotech.in

Hello There,

Greetings from Health Biotech Limited!

We are one of the leading Indian Pharmaceutical Manufacturer & Exporter of finished formulations. Our state-of-the-art, WHO-GMP certified manufacturing facilities
are located in the industrial town of Baddi, in the State of Himachal Pradesh, India.

We are a global exporter and kindly contact us for mentioned requirement.

Thanks,

Jay
Health Biotech Limited
+91 987-688-2973
enquiry@healthbiotech.in
www.healthbiotech.in

17:56,  07 Sep 2022

smit@salvavidaspharma.com

Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers and it can be available with us.
can we connect for some business?

Please, contact
smit@salvavidaspharma.com
Mo: +91 74359 19702 (Whatsapp : https://wa.link/8hjiee )
(Telegram : https://t.me/smit_slavavidas )

14:34,  10 Sep 2022

marketing@vktpharma.com

Hi, We hold EU & WHO-GMP approval for our OSD site in India. Please reach us out on marketing@vktpharma.com

10:44,  12 Sep 2022

bd@pharminterface.com

Dear Sir/Madam

We Pharm Interface a leading pharma company from India which provides all Finished Formulations, APIs and Excipients with all the supporting documents. We offer it with best price. please go through our website. link is given below

Thanks & Regards
Priya Patil
Email - priya.p@pharminterface.com
website - https://pharminterface.com

20:59,  29 Sep 2022

bd@pharminterface.com

Dear Sir/Madam

Which product do you require. we can provide

Thanks & Regards
Priya Patil
Email - priya.p@pharminterface.com
website - https://pharminterface.com

21:04,  29 Sep 2022

marketing@vktpharma.com

I’m reaching to you for evaluating to support on contract manufacturing opportunity from VKT’s site. The brief intro of company is enclosed along with highlights below.

• An oral solid finished dosage manufacturer with USFDA & EU-GMP approvals
• Annual manufacturing capacity of 4Bn OSDs (Non-Onco: Tablets & Capsules)

11:25,  10 Oct 2022

70284@yangzijiang.com

We have EUGMP approved facility for solid product. Please send me a email for CMO proposal.

11:46,  05 Jan 2024
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