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Formulation
Fundamentals of formulation and manufacturing of Pharmaceutical Dosage Forms
Quality By Design/ QBD for Experiments
Warehouse
Good Storage practice
Warehouse Management
Laboratory and Analysis
Analytical Method validation
HPLC basic principles and advanced course
HPLC trouble shooting advanced
Microbiology in Pharma Industry
HPLC Method development
Excel Spreadsheet Design and Validation
Gas Chromatography (GC) basic principles
ISO Accreditation, training and preparation
ISO 45001
ISO 14001:2015 Environmental management system (EMS)
ISO 9001:2015 – Quality management systems
Business continuity management in pharmaceutical industry ISO 22301:2012
GMP and GLP
Advanced cGMP / cGMP auditing.
Basic principles on Sanitation & Hygiene Practices in GMP
Good Manufacturing practice (GMP) for new pharmacists and chemists
Good Laboratory Practice and Laboratory management system
Good Manufacturing practice (GMP) for Workers and technicians
Quality management system and Quality Compliance
Pharmaceutical Quality management system
Risk Management
Good documentation practice and Documentation system control
In process Control (Roles, How and Why)
Data Integrity and Governance
TQM basics
Validation and Qualification
Cleaning validation and hold time studies.
Process validation Bulk hold time studies
Computer System validation
Validation for Workers and technicians
thermal mapping studies
Good weighing practice Balance Qualification
Statistical process control and control charts
HVAC and Premises Qualification
Calibration management
Equipment & Water system qualification
Stability
Pharmaceutical Quality management system
Audit preparation
How to deal with Audits
Preparation of WHO, FDA & EMA audits
Under-Graduate
Orientation for Manufacturing Industry
Events
My Account
Contact
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Home
About
Courses
Formulation
Fundamentals of formulation and manufacturing of Pharmaceutical Dosage Forms
Quality By Design/ QBD for Experiments
Warehouse
Good Storage practice
Warehouse Management
Laboratory and Analysis
Analytical Method validation
HPLC basic principles and advanced course
HPLC trouble shooting advanced
Microbiology in Pharma Industry
HPLC Method development
Excel Spreadsheet Design and Validation
Gas Chromatography (GC) basic principles
ISO Accreditation, training and preparation
ISO 45001
ISO 14001:2015 Environmental management system (EMS)
ISO 9001:2015 – Quality management systems
Business continuity management in pharmaceutical industry ISO 22301:2012
GMP and GLP
Advanced cGMP / cGMP auditing.
Basic principles on Sanitation & Hygiene Practices in GMP
Good Manufacturing practice (GMP) for new pharmacists and chemists
Good Laboratory Practice and Laboratory management system
Good Manufacturing practice (GMP) for Workers and technicians
Quality management system and Quality Compliance
Pharmaceutical Quality management system
Risk Management
Good documentation practice and Documentation system control
In process Control (Roles, How and Why)
Data Integrity and Governance
TQM basics
Validation and Qualification
Cleaning validation and hold time studies.
Process validation Bulk hold time studies
Computer System validation
Validation for Workers and technicians
thermal mapping studies
Good weighing practice Balance Qualification
Statistical process control and control charts
HVAC and Premises Qualification
Calibration management
Equipment & Water system qualification
Stability
Pharmaceutical Quality management system
Audit preparation
How to deal with Audits
Preparation of WHO, FDA & EMA audits
Under-Graduate
Orientation for Manufacturing Industry
Events
My Account
Contact
Business continuity management in pharmaceutical industry ISO 22301:2012
