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sam.d@micoson.com
we would like to participate in the quotation and Please send your email to sam.d@micoson.com. We will reply to the quotation within 7 hours,
Thank you for your support.
Monica.Oneglio@adareps.com
Dear sirs,
Adare Pharma Solutions is expert in contract development and manufacture of Multi particulate oral dosage forms.
Our technology expertise comprises:
• Microcaps® taste-masking (we are the leader in organic coacervation by micro-encapsulation) to be combined with
- Advatab® orally disintegrating tablets (fast disintegrating but robust tablets, made of finely micronized manitol, thus superior mouth feel)
- Liquitard® sachet formulation (ideal for pediatric, geriatric and dysphagic patients)
• Controlled release formulations
- MMTSTM - Multi Mini Tablet System: 1-2 mm small coated minitablets, ideal to address pediatric patients
- Diffucaps® drug beads layered with one or more functional polymers for sophisticated drug release profiles (once daily, several pulses, chronotherapy)
• BioriseTM bioavailability enhancement of purely soluble drugs
Adare can provide clear differentiation advantages: we can resolve formulation challenges, improve patient convenience, address pediatric and geriatric patient populations, enable new therapeutic uses and support life cycle management of your product including the extension of patent exclusivity.
We are committed to partnering with innovators in the pharmaceutical industry: over 40 products incorporating our technologies have been commercialized by our partners around the world.
Facilities:
Adare Pharma Solutions has four sites located in the US and Europe with over 600 employees worldwide. We have the expertise to take your project from formulation development through commercial scale manufacturing. Our sites are compliant with cGMP criteria and approved to handle controlled substances and maintain excellent environmental credentials. Our in house regulatory and quality teams have a proven global track record with the FDA, AIFA in Italy, EMA in Europe and ANVISA for Brazil.
I am looking forward to hearing from you soon.
https://www.adarepharmasolutions.com/
With my best regards
Monica Oneglio
BD Associate EU
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
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
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
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...!!!
