Kind Note:
For Enquires please contact via
+91 8317692733/9642837599
(No calls please)
(OR) Through
Email:
contact@sadhanainfotech.com
. We shall approach you within 24 hours.
An IS0 9001:2015 Certified Institute
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About Us
Courses Offered
ENTRY LEVEL RA
MIDDLE LEVEL RA
PROFESSIONAL LEVEL RA
EXPERT LEVEL RA
Dossier/ANDA Compilation training Program
CRASH COURSE
PHARMACOVIGILANCE (PV)
Aggregate Reporting
Clinical Research
Pharmaceutical Drug Development
Drug Substances (API)
Drug Approval procedure in US and EU
PHARMA VALIDATION
Quality Assurance
Quires & Approval Changes
THIRD PARTY DOSSIER PREPRATION
THIRD PARTY QUIRES AND POST APPROVAL CHANGES
Student Placements
Our Services
Regulatory Intelligence
Regulatory Strategy & Reports
CMC Regulatory Affairs
Dossier Preparation and Submissions of New Marketing Authorizations
Post Licensing Activities
Medical writing
Publishing and Submissions
GMP Auditing for the Pharmaceutical Industry
Total Services by Sadhana Infotech
Careers
Blog
Contact Us
Home
About Us
Courses Offered
ENTRY LEVEL RA
MIDDLE LEVEL RA
PROFESSIONAL LEVEL RA
EXPERT LEVEL RA
Dossier/ANDA Compilation training Program
CRASH COURSE
PHARMACOVIGILANCE (PV)
Aggregate Reporting
Clinical Research
Pharmaceutical Drug Development
Drug Substances (API)
Drug Approval procedure in US and EU
PHARMA VALIDATION
Quality Assurance
Quires & Approval Changes
THIRD PARTY DOSSIER PREPRATION
THIRD PARTY QUIRES AND POST APPROVAL CHANGES
Student Placements
Our Services
Regulatory Intelligence
Regulatory Strategy & Reports
CMC Regulatory Affairs
Dossier Preparation and Submissions of New Marketing Authorizations
Post Licensing Activities
Medical writing
Publishing and Submissions
GMP Auditing for the Pharmaceutical Industry
Total Services by Sadhana Infotech
Careers
Blog
Contact Us
Blog
Home
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Date:
01 January 1970
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