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Biomedical Industrial and Academic Training
Certification Course in Medical Device Quality Management System
Certification Course in QMS Documentation of Medical Devices
ISO 13485:2016 Internal Auditor Course
IRCA-CQI Approved ISO 13485:2016 Lead Auditor Course
Certification Course in Biomedical Equipment Installation & Servicing
Certification Course in IVD Medical Devices Installation & Servicing
Certification Course to Become Expert in Single Point Department
Regular Professional Certification Courses
Pharmaceutical
Advanced Course in GLOBAL REGULATORY AFFAIRS
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 (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
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 Q1-Stability Studies
ICH Q2-Analytical Validation
ICH Q3-Impurities
ICH Q6-Specification
ICH Q9-Quality Risk Management
ICH Q10-Pharmaceutical Quality Management
Importance of Data Integrity in Pharmaceuticals
Nutraceuticals
Regulatory Perspective of Nutraceuticals
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+91 994 695 1960
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