09 Feb 2021

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Tender// Filgrastim Solution for Intravenous and Subcutaneous Administration needed in Russia [ENA09688]
State Budgetary Institution of Health Care of the Moscow Region “Moscow Regional Oncological Dispenser” is looking for supplies of Filgrastim (300 ug/ ml) Solution for Intravenous and Subcutaneous Administration. The required quantity is 3,750 units. The deadline is 16-Feb-2021.

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info@aeqpharma.com

please contac us.
We have vialsfrom germany

13:08,  09 Feb 2021

vishvesh.shaishav@gmail.com

We are focussed on developing new manufacturing technologies, including custom synthesis of new moleculepharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, pharmaceutical pellets,additives, contract manufacturing, chemicals. We began in the field of specialty intermediates for pharmaceutical applications and developed our own purification technologies for manufacturing highly pure intermediates. And Pharmaceutical API At a later stage, we integrated forward to manufacture finished formulations for both veterinary and human consumption. Due to our completely integrated operations in the pharmaceutical sector, we continuously learn about the quality parameters for an API based on the performance of the finished formulation in order to quality their Bioequivalence Studies.
We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.
Our focus lies in developing new production technologies with a keen interest in frugal innovation in order to gain a competitive edge over others. We specialize in the custom synthesis of molecules and work with many reputed companies around the world on an OEM basis.pharmaceutical pellets,Intermidiates
Our finished formulations from WHO-GMP and EU-GMP units are registered/being registered in 26 countries within Asia, Europe, North America, Latin America and Africa continents including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad, Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.
vishvesh.shaishav@gmail.com

22:58,  10 Feb 2021

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  

23:58,  16 Feb 2021

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

07:47,  19 Feb 2021
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