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akansha.chauhan@apicore.com
Kindly provide full product detail with CAS number.
info@indeximinternational.com
ndexim international, are one of the leading supplier, exporter and importer of Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard,, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements. Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian countries 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.
Indexim International
sales.indeximinternational@gmail.com
info@indeximinternational.com
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
We are a Pharmaceutical Company from UAE and we can supply you.
Contact us: ph@alnamatalalamy.com
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
trupti.joshi@meghmanigroup.com
Dear Sir,
Greetings from Meghmani LLP !!
Meghmani LLP is a part of Meghmani Group of companies, and we aim to become one of India’s Leading pharmaceutical companies with our state-of-the-art manufacturing facility complying with USFDA standards and dedicated to one single Active Pharmaceutical Ingredient (API) “PARACETAMOL”. This facility is located at “Dahej”, State: Gujarat, India, an upcoming and Largest Industrial Zone in the western part of India, 400 KM away from Mumbai.
REGULATORY APPROVALS:
Our facility is WHO-GMP approved, and we have filed for USDMF (DMF No: 030244). Further we have Received CEP certification from EDQM (Dossier No: CEP 2015-377-Rev01). Besides this we have ISO-14001; OHSAS-18001 & WCC certifications. We have available ODMF for EDMF and USDMF.
email address: trupti.joshi@meghmanigroup.comphone
number: +91 9408418091
Our vision is to become a well-respected global player and an undisputed leader in
“PARACETAMOL” market both in terms of manufacturing capacity as well as sales Quantum.
Thanking you with regards,
Your Sincerely,
Trupti Joshi
MEGHMANI LLP
trupti.joshi@meghmanigroup.com
Dear Sir,
Greetings from Meghmani LLP !!
Meghmani LLP is a part of Meghmani Group of companies, and we aim to become one of India’s Leading pharmaceutical companies with our state-of-the-art manufacturing facility complying with USFDA standards and dedicated to one single Active Pharmaceutical Ingredient (API) “PARACETAMOL”. This facility is located at “Dahej”, State: Gujarat, India, an upcoming and Largest Industrial Zone in the western part of India, 400 KM away from Mumbai.
REGULATORY APPROVALS:
Our facility is WHO-GMP approved, and we have filed for USDMF (DMF No: 030244). Further we have Received CEP certification from EDQM (Dossier No: CEP 2015-377-Rev01). Besides this we have ISO-14001; OHSAS-18001 & WCC certifications. We have available ODMF for EDMF and USDMF.
email address: trupti.joshi@meghmanigroup.comphone
number: +91 9408418091
Our vision is to become a well-respected global player and an undisputed leader in
“PARACETAMOL” market both in terms of manufacturing capacity as well as sales Quantum.
Thanking you with regards,
Your Sincerely,
Trupti Joshi
MEGHMANI LLP
trupti.joshi@meghmanigroup.com
Dear Sir,
Greetings from Meghmani LLP !!
Meghmani LLP is a part of Meghmani Group of companies, and we aim to become one of India’s Leading pharmaceutical companies with our state-of-the-art manufacturing facility complying with USFDA standards and dedicated to one single Active Pharmaceutical Ingredient (API) “PARACETAMOL”. This facility is located at “Dahej”, State: Gujarat, India, an upcoming and Largest Industrial Zone in the western part of India, 400 KM away from Mumbai.
REGULATORY APPROVALS:
Our facility is WHO-GMP approved, and we have filed for USDMF (DMF No: 030244). Further we have Received CEP certification from EDQM (Dossier No: CEP 2015-377-Rev01). Besides this we have ISO-14001; OHSAS-18001 & WCC certifications. We have available ODMF for EDMF and USDMF.
email address: trupti.joshi@meghmanigroup.comphone
number: +91 9408418091
Our vision is to become a well-respected global player and an undisputed leader in
“PARACETAMOL” market both in terms of manufacturing capacity as well as sales Quantum.
Thanking you with regards,
Your Sincerely,
Trupti Joshi
MEGHMANI LLP
trupti.joshi@meghmanigroup.com
Dear Sir,
Greetings from Meghmani LLP !!
Meghmani LLP is a part of Meghmani Group of companies, and we aim to become one of India’s Leading pharmaceutical companies with our state-of-the-art manufacturing facility complying with USFDA standards and dedicated to one single Active Pharmaceutical Ingredient (API) “PARACETAMOL”. This facility is located at “Dahej”, State: Gujarat, India, an upcoming and Largest Industrial Zone in the western part of India, 400 KM away from Mumbai.
REGULATORY APPROVALS:
Our facility is WHO-GMP approved, and we have filed for USDMF (DMF No: 030244). Further we have Received CEP certification from EDQM (Dossier No: CEP 2015-377-Rev01). Besides this we have ISO-14001; OHSAS-18001 & WCC certifications. We have available ODMF for EDMF and USDMF.
email address: trupti.joshi@meghmanigroup.comphone
number: +91 9408418091
Our vision is to become a well-respected global player and an undisputed leader in
“PARACETAMOL” market both in terms of manufacturing capacity as well as sales Quantum.
Thanking you with regards,
Your Sincerely,
Trupti Joshi
MEGHMANI LLP
trupti.joshi@meghmanigroup.com
Dear Sir,
Greetings from Meghmani LLP !!
Meghmani LLP is a part of Meghmani Group of companies, and we aim to become one of India’s Leading pharmaceutical companies with our state-of-the-art manufacturing facility complying with USFDA standards and dedicated to one single Active Pharmaceutical Ingredient (API) “PARACETAMOL”. This facility is located at “Dahej”, State: Gujarat, India, an upcoming and Largest Industrial Zone in the western part of India, 400 KM away from Mumbai.
REGULATORY APPROVALS:
Our facility is WHO-GMP approved, and we have filed for USDMF (DMF No: 030244). Further we have Received CEP certification from EDQM (Dossier No: CEP 2015-377-Rev01). Besides this we have ISO-14001; OHSAS-18001 & WCC certifications. We have available ODMF for EDMF and USDMF.
email address: trupti.joshi@meghmanigroup.comphone
number: +91 9408418091
Our vision is to become a well-respected global player and an undisputed leader in
“PARACETAMOL” market both in terms of manufacturing capacity as well as sales Quantum.
Thanking you with regards,
Your Sincerely,
Trupti Joshi
MEGHMANI LLP
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
