Gap Analysis

Gap Analysis

Now a day’s qualifying regulatory inspections and audits is becoming more and more difficult and challenging. Though you are maintaining GMP compliant systems but not able to understand any major gaps and lac in quality management systems. Sometimes you are not sure whether implementations with GMP, GLP and other regulatory requirements. You need to third eye/independent technical experts needs to identify the gaps in Quality systems, reporting observations, finding and recommendations, implementation and continue monitoring for continual improvements , Geekay Pharmagreen under the aegis of Mr. Girish Maheswari’s strong understanding of this field given his 35+ (plus) years of experience can lead your company by performing a comprehensive Gap analysis in almost all topics determining gaps
through Audits for following;

– Good Manufacturing Practices (GMP)
– USFDA, CFR Part 210,211, Part 117, 110,111
– Good Laboratory practices
– NABL Certifications
– PIC,s, MHRA, WHO GMP,TGA, MHRA
– Facility Feasibility analysis
– Data Integrity
– Good Documentation Practices

If you want our support then don’t delay to communicate with our experts and let us help you out with finest services.