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            Email Us : info@zodiacpharma.com        For Technical Help : +91-96-52-281814
Analytical Validation      Dossiers      DMF      Stablity Studies      Product Development       Training        Facility
Zodiac Pharma is an International Regulatory Affairs / Registration Dossier consulting firm and Analytical Research Laboratory based at India.  In Year 2008, Zodiac Pharma was Founded by Mr. Tara chand Tak (CEO), a technocrat with regulatory affair (dossier) experience in the pharmaceutical industry.

Our Facility (Dossier Developing, Dossier Prepration, Analytical Reserach & Formulation Development) Located at:-

Zodiac Pharma,
Plot No. 63, 76 & 77,
Industrial Park (APIIC) Valasapalli,
Madanapalle Mandal -517 325,
Chittoor Dist. (Andhra Pradesh) India

Our Core Services

  • Registration Dossier (Regulatory affairs)
  • Analytical Method Validation
  • European CTD/ ASEAN CTD Dossier
  • BE studies
  • Training


Why Zodiac Pharma

  • In-house Facility (Reserach & Dossier Developing)
  • Technical Expertise
  • Complete database
  • Quality services
  • On-time delivery
  • Complete dossier solution



Andhra Pradesh
Arunachal Pradesh
Assam
Bihar
Chhattisgarh
Goa
Gujarat
Haryana
Himachal Pradesh
Jammu and Kashmir
Jharkhand
Karnataka
Kerala
Madhya Pradesh
Maharashtra
Manipur
Meghalaya
Mizoram
Nagaland
Orissa
Punjab
Rajasthan
Sikkim
Tamil Nadu
Tripura
Uttar Pradesh
Uttarakhand
West Bengal



Zodiac Pharma :- Your Key Partner for Export Product Registration
In-house Dossier Development Facility
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Dossier Services for more than 85 countries
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PSUR -Periodic Safety Update Reports
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Ready CTD / ASEAN CTD dossiers
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Free consultation: - pre-product registration / pre-dossier preparation inquiries
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Analytical Method Validation (Formulation and API)
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Special reduced charges for Pharmaceutical SMEs and small manufacturer
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Regulatory training for Industries and Academic
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Dossier conversion (from one country to another)
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Ready dossier available for Asian, African and CIS market (CTD or Non-CTD dossier)
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Dossiers as per ASEAN CTD Guideline
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Dossier in EUCTD format
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Dossier as per latest regulatory guidelines (released by MOH)
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Dossier Preparation: - Africa, Asia, CIS, Europe, Central America, North America, South America
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Stability Studies - Real time and Accelerated stability studies
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Process validation
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Complete regulatory assistance till the registration stage
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Pharmaceutical Technology - Know How
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Assistance for Product Development
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SmPC, Pack insert and PIL preparation
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Clinical and Non-clinical Overviews and Expert Report
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EUCTD and ASEAN CTD dossiers compilation and review
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Dossier Developing Unit
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Patent Cell
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Bioequivalence Studies
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Animal Toxicological Studies
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Professional Training for corporate top management, industrial staff and college students
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European-CTD / ICH - CTD Dossier Compilation for regulated market
Zodiac Pharma- Your Export Partner

When Nobody Can ! 

''WE CAN''