RAAJ GPRAC /RaajpharmaeLearning Affiliated by Etherea Global University, USA !! and Accredited as per ISO 20001-2018. For more details, please contact on
9819125208
/
9821144706
||
Professional certification course in Pharma, Medical device and Nutraceutical.
Click Here
||
RAAJ Pharma Short Courses
Click Here
||
Raaj pharma eLearning More Courses
Click Here
||
Admission Form
KNOWLEDGE ONLINE
About Us
Overview
Expertise
Webinar
Career
FAQs
Services
Regulatory Services
GxP Compliances
Audits
Quality Systems
Labelling Management
Documentation & Records
Product Life Cycle
Validations
Training
Common Technical Document
DMF
Pharmacovigilance
Medical Writing
Training
On-site Off-Shore Training
Courses
Regular Professional Certification Courses
Pharmaceutical
Advanced course in GLOBAL REGULATORY AFFAIRS [GRA-API, Formulations, Medical Devices, Biosimilars, OTC]
REGULATORY AFFAIRS-Formulation
REGULATORY AFFAIRS-API[DMF/ASMF/CEP]
QA-QM [ Quality Assurance and Quality Management]
Regulatory Submissions as per CTD-eCTD, ACTD , NeeS
Advanced course in Clinical Research[CR]
Advanced course in Documentation [PD]
Advanced course in Pharmacovigilance [PV]
Advanced course in Patents Laws and Procedures [IPR]
Advanced course in Pharmaceutical Management[PM]
Advanced course in Medical Writing [MW]
Stability Testing in Pharmaceuticals
Effective CMC Writing and Review Skills
Nutraceuticals
Advanced course in NUTRACEUTICALS[NUTRA]
Medical Device
GLOBAL Medical Devices Regulations i.e. MDR course[India, Europe, USA, ASEAN, ROW markets]
Medical Device-Quality Assurance
Internal Auditor/Lead Auditor QMS 13485-2016, ISO 19011-2018 Course
Medical Device -Indian Regulation, Bis Submission, Sugam Portal Submission
Medical Device-European MDR, CE Mark
Medical Device- USFDA Submission
MDD to MDR Implementation
Medical Device-Risk Management
Implementation of MDSAP, An Overview
Raajpharma eLearning Short Courses
Medical Device
Biologics/Biosimilar Submission as per US and EU
Medical Device labeling as per EU and ISO 15223
Pharmaceutical Product labeling as US, EU and India
Computer System Validation, 21 CFR part 11, GAMP 5
Internal Auditor/Lead Auditor QMS 13485-2016, ISO 19011-2018 Course
Medical Device -Indian Regulation, BIS Submission, Sugam Portal Submission
Medical Device-European MDR, CE Mark
Medical Device- USFDA Submission
MDD to MDR Implementation
Medical Device-Risk Management
Medical Device Design and Development
Pharmaceutical
Effective CMC Writing and Review Skills
Drug Regulation In US
Drug Regulation in Europe
Drug Regulation in ROW
Drug Substance Regulation-Drug Master File
Formulation Development
Drug Development Process
Good Manufacturing Practice
Regulatory System in Canada
ICH Q 1-Stability Studies
ICH Q2-Analytical Validation
ICH Q3-Impurities
ICH Q 6-Specification
ICH Q9- Quality Risk Management
ICH Q10- Pharmaceutical Quality Management
Importance of Data Integrity in Pharmaceuticals
Nutraceuticals
Regulatory Perspective of Nutraceuticals
Resources
Useful Links
Library
Testimonial
Students
Industry Experts
Testimonial
Photo Gallery
Achievements
2024 Years
2023 Years
2022 Years
2021 Years
2020 Years
2019 Years
2018 Years
2017 Years
2016 Years
2015 Years
2014 Years
2013 Years
2012 Years
Videos
E-learning
Videos Testimonial
Blog
Contact Us
Industy Updates
Contact
Visit Our other Website
Home
Achievement 2017
We thank each and every participant
for making this event grand success.
//
Janaury, 2017
//
Show the Achivements.
