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GMP In-house Training Programme
for the Pharmaceutical, API and Medical Device Industry

 
Subject of the Training Course Number of Days
Basic GMP  
Basic GMP Course Regulatory and GMP Requirements for Pharmaceutical Companies (e-mail inquiry) 1
Good Distribution Practice (GDP)  
Good Storage Practice (e-mail inquiry) 1
Good Distribution Practice
(Storage, Transportation, Cold Chain)
(e-mail inquiry)
2
Quality Control  
FDA and EU GMP Compliance in analytical Laboratories (e-mail inquiry) 2
Stability Testing in the Pharmaceutical Industry (e-mail inquiry) 2
Out-of-Specification Results (e-mail inquiry) 2
Quality Assurance  
Data Integrity Course (e-mail inquiry) 1
Deviation, Failure Investigation, Annual Product Review and Change Management (e-mail inquiry) 1
Auditing / Self-Inspection (e-mail inquiry) 1
Quality Assurance Systems Based on ISO 9001 and GMP  
(e-mail inquiry)
1
Change Management - Changes and Deviations (e-mail inquiry) 1
Good Storage Practice (e-mail inquiry) 1
GMP and FDA Compliance in Quality Assurance Units  
(e-mail inquiry)
2
Pharmaceutical Quality Systems (e-mail inquiry) 2
Hygiene Training Course (e-mail inquiry) 2
IT/Computer Validation  
Regulatory Compliance for IT Professionals (e-mail inquiry) 1
Validating Computerised Analytical Equipment and Systems  
(e-mail inquiry)
2
Electronic Records and Electronic Signatures (21 CFR Part 11) (e-mail inquiry) 1
New EU GMP Annex 11 Regulations for Computerised Systems (e-mail inquiry) 2
Validation/Qualification  
Qualification and Validation of Equipment and Processes in Laboratories and Manufacturing (e-mail inquiry) 2
Basic GMP Training Qualification/Validation (e-mail inquiry) 1
Cleaning Validation in Pharmaceutical Drug Product and API Production (e-mail inquiry) 2
Sterile Manufacture  
Production of Sterile Pharmaceuticals (e-mail inquiry) 2
Good Clinical Practice  
Basic Course in Good Clinical Practice (e-mail inquiry) 1/2
Medical Devices  
Regulatory Requirements on Medical Devices (e-mail inquiry) 1
APIs  
ICH Q7A Compliance (e-mail inquiry) 2
Regulatory Affairs  
Regulatory Structure
Regulatory Requirements for Pharmaceutical Companies
 
(e-mail inquiry)
1
The Regulatory Aspects of Validation and Implementation of a New Technology  
(e-mail inquiry)
1
Steps from Drug Development to Marketing Authorisation  
(e-mail inquiry)
1
Marketing Authorisations and Post-Approval Obligations in the EU  
(e-mail inquiry)
2
Quality Data in the Marketing Authorisation Application  
(e-mail inquiry)
1

 

 GMP Conferences by Topics
 Quality Assurance
 GMP in Biotechnology
 Microbiology
 Regulatory Affairs
 GMP in Pharmaceutical Development
 Quality Control
 Storage, Distribution, Transportation
 Sterile / Aseptic Manufacturing
 Computer Validation
 Technical Operations
 GMP for APIs and Excipients
 Validation
 Medical Devices
 GMP Basic Training Courses
 Packaging