Pharmaceutical Industries and GMP

No. Title Course Code Delivery Language Hours of Training Days Training
1 Global regulatory framework 210001 E/A 4 1
2 Regulation and guidance 210002 E/A 4 1
3 Mutual recognition agreements, Regulatory inspections, Enforcement actions, Regulatory agency reporting 210003 E/A 4 1
4 Site master file (SMF) and Drug master file (DMF) 210004 E/A 12 3
5 Quality management system (QMS), ICH Q 10 210005 E/A 16 4
6 Risk management 210006 E/A 8 2
7 Training and personal qualification 211025 E/A 4 1
8 Pharmaceutical dosage forms 210007 E/A 4 1
9 SIX Sigma in pharmaceutical industry 210008 E/A 16 4
10 Requalification program 210009 E/A 12 3
11 Change control and management   E/A 4 1
12 Corrective and preventive action (CAPA) 211100 E/A 4 1
13 Audits and self inspections   E/A 4 1
14 Documents and records management 211180 E/A 4 1
15 Product quality complaints 211196 E/A 4 1
16 Product trend requirements   E/A 4 1
17 Supplier and contractor qualification   E/A 4 1
18 Compendia   E/A 4 1
19 Laboratory investigations of aberrant results   E/A 4 1
20 Instrument control and record –keeping 211182 E/A 4 1
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