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× PREPARATION, APPROVAL, REVIEW AND CONTROL OF TECHNICAL DIRECTIONS FOR MANUFACTURE OF PHARMACEUTICAL PRODUCTS PREPARATION, APPROVAL, REVIEW AND CONTROL OF TECHNICAL DIRECTIONS FOR MANUFACTURE OF PHARMACEUTICAL PRODUCTS 9.00
9.00
× 6M-Based Investigation on Tablet Chipping at Compression Stage 6M-Based Investigation on Tablet Chipping at Compression Stage 50.00
50.00
× RELEASE OF BATCHES FOR PACKING AND SALE RELEASE OF BATCHES FOR PACKING AND SALE 9.00
9.00
× Standard Operating Procedure for New Product Introduction in Facility Standard Operating Procedure for New Product Introduction in Facility 15.00
15.00
× QUALITY RISK ASSESSMENT (QUALITY METRICS) IN PHARMACEUTICAL QUALITY RISK ASSESSMENT (QUALITY METRICS) IN PHARMACEUTICAL 15.00
15.00
× INVESTIGATION REPORT FOR THE OBSERVATION OF RAW MATERIAL FROM UNAPPROVED VENDOR IN RM WAREHOUSE INVESTIGATION REPORT FOR THE OBSERVATION OF RAW MATERIAL FROM UNAPPROVED VENDOR IN RM WAREHOUSE 15.00
15.00
× INVESTIGATION REPORT FOR MARKET COMPLAINT FOUND GHOST PILLS (EMPTY SHELLS) IN STOOL INVESTIGATION REPORT FOR MARKET COMPLAINT FOUND GHOST PILLS (EMPTY SHELLS) IN STOOL 15.00
15.00
× INVESTIGATION REPORT FOR THE OBSERVATION OF BLACK PARTICLE IN COMPRESSED TABLET AFTER COMPRESSION INVESTIGATION REPORT FOR THE OBSERVATION OF BLACK PARTICLE IN COMPRESSED TABLET AFTER COMPRESSION 50.00
50.00
× Self Inspection In Pharmaceutical Self Inspection In Pharmaceutical 11.00
11.00
× INVESTIGATION REPORT FOR THE OBSERVATION OF DIFFERENTIAL PRESSURE OUT OF LIMIT INVESTIGATION REPORT FOR THE OBSERVATION OF DIFFERENTIAL PRESSURE OUT OF LIMIT 15.00
15.00
× PREPARATION AND CONDUCTION OF GMP AUDIT INSPECTION BY REGULATORY AUTHORITY OR CUSTOMER PREPARATION AND CONDUCTION OF GMP AUDIT INSPECTION BY REGULATORY AUTHORITY OR CUSTOMER 9.00
9.00

Cart totals

Subtotal 213.00
Total 213.00