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Metina PharmConsulting | Global Pharma Regulatory Services

Metina is a Global Regulatory Affairs Pharm Consulting firm having expertise in submissions and approvals for USA, EU and Emerging Markets.

http://www.metinapharmconsulting.com/

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Metina PharmConsulting | Global Pharma Regulatory Services | metinapharmconsulting.com Reviews
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Metina is a Global Regulatory Affairs Pharm Consulting firm having expertise in submissions and approvals for USA, EU and Emerging Markets.
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1 Pharm Consulting
2 Regulatory Affairs
3 Metina Consulting
4 Mumbai
5 Navi Mumbai
6 Filing for ANDA
7 NDA
8 NCE
9 FDA Submission
10 End-to-End Regulatory Services
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regulatory submissions,regulatory strategy,product development,gmp inspections,technology transfer,global capabilities,financial institutions consulting,japanese,about us,company profile,founder's profile,our blog,careers,testimonials,learn more about
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Metina PharmConsulting | Global Pharma Regulatory Services | metinapharmconsulting.com Reviews

https://metinapharmconsulting.com

Metina is a Global Regulatory Affairs Pharm Consulting firm having expertise in submissions and approvals for USA, EU and Emerging Markets.

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1

Metina PharmConsulting | Metina Japan

http://www.metinapharmconsulting.com/metina-japan.php

Regulatory tools and Medical Writing. Due Dilligence of technical dossier. Drug master file (dmf). Ctd / national dossiers. Submission to health authority and approval. Product life cycle management. Visit us at IPHEX 2016, Hall 1- Stall B 14. 27th 29th April 2016, Bombay Exhibition Centre. METINA PHARMCONSULTING PVT.LTD. 1306, Mayuresh Chambers, Sector 11,. Central Business District (CBD) Belapur,. Navi Mumbai, 400614 Maharashtra, India. Tel : 91 22 6793 0000 / 4012 6898. Fax : 91 22 67939919.

2

Metina PharmConsulting | Regulatory Tools and Medical Writing

http://www.metinapharmconsulting.com/regulatory-tools.php

Regulatory tools and Medical Writing. Due Dilligence of technical dossier. Drug master file (dmf). Ctd / national dossiers. Submission to health authority and approval. Product life cycle management. Visit us at IPHEX 2016, Hall 1- Stall B 14. 27th 29th April 2016, Bombay Exhibition Centre. Regulatory Tools and Medical Writing. We can provide following regulatory documents:. Check list of documents in line with prevalent regulatory submission guidelines for Marketing Authorization Application across Globe.

3

Metina PharmConsulting | Financial Institutions Consulting | Corporate Debt Restructuring

http://www.metinapharmconsulting.com/financial-institutions-consulting.php

Regulatory tools and Medical Writing. Due Dilligence of technical dossier. Drug master file (dmf). Ctd / national dossiers. Submission to health authority and approval. Product life cycle management. Visit us at IPHEX 2016, Hall 1- Stall B 14. 27th 29th April 2016, Bombay Exhibition Centre. Metina provides following services to financial institutions (Banks):. Regulatory Inspection of the Pharmaceutical Company. Verification and Validation of Regulatory Approvals. Activities to fulfill CDR formalities.

4

Metina PharmConsulting | Submissions to Health Authorities and Approval

http://www.metinapharmconsulting.com/submission-health-authority.php

Regulatory tools and Medical Writing. Due Dilligence of technical dossier. Drug master file (dmf). Ctd / national dossiers. Submission to health authority and approval. Product life cycle management. Visit us at IPHEX 2016, Hall 1- Stall B 14. 27th 29th April 2016, Bombay Exhibition Centre. Submission to Health Authority. Submission to Health Authority and Approval. Electronic / Paper technical data preparation with local forms/application and actual submission to respective Health Authority.

5

Metina PharmConsulting | Regulatory Services

http://www.metinapharmconsulting.com/regulatory-submissions.php

Regulatory tools and Medical Writing. Due Dilligence of technical dossier. Drug master file (dmf). Ctd / national dossiers. Submission to health authority and approval. Product life cycle management. Visit us at IPHEX 2016, Hall 1- Stall B 14. 27th 29th April 2016, Bombay Exhibition Centre. Regulatory Tools and Medical Writing. Due Diligence of Technical Dossier. Drug Master File (DMF). CTD / National Dossiers. Submission to Health Authority. Product Life Cycle Management. Fax : 91 22 67939919.

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Web Design Company Testimonials|Ornus Client Testimonials

http://www.ornusweb.com/what_clients_say.html

What Our Client's Say. Omtex Sports Academy Pvt. Ltd. (Mumbai, India). Ornus promised to design, develop and deliver our website within 7 days to meet our official launch and press conference. And they delivered well before time! Metina PharmConsulting Pvt. Ltd. (Mumbai, India). Trust me this is first time I am feeling happy and excited about Website going LIVE! This is all because of ORNUS constant support, guidance and understanding of our requirements throughout the period. Sandeep and his team have d...

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