Micro Labs Limited is an Indian pharmaceutical company founded in 1973 that describes itself as "a technology-focused, multi-dimensional pharmaceutical company" with manufacturing across diverse therapeutic areas. It runs 14 manufacturing plants and states a presence in over 50 countries with ground-level operations in 25. Its API unit at Bommasandra, Bangalore is a 24,000 square metre facility staffed by 280 employees, around 200 of them technical and scientific.
Compliance iCounts agency registrations (FDA, EU GMP, MHRA, PMDA, WHO GMP, NMPA, PIC/S) at 6 points each capped at 35, ISO certifications at 5 each capped at 20, GMP status (cGMP commercial 25, GMP 18, Pharma-grade 10), plus DMF 7, CEP 7 and TSE/BSE statement 6. Levels: 80+ Fully GMP-compliant | 60-79 GMP-compliant | 40-59 Developing compliance | below 40 Research-grade. Whether this dimension matters for you depends on your specific project.
43Developing compliance
Quality iBlends the reported audit score (up to 40 points), CAPA closure rate (up to 25) and deviation history (starts at 20 and loses 2 points per deviation), plus 8 for CoA availability and 7 for validation packages. Levels: 85+ Excellent quality | 65-84 Strong quality | 45-64 Good quality | below 45 Developing. Whether this dimension matters for you depends on your specific project.
—Not disclosed
Delivery iBlends on-time delivery percentage (up to 50 points), lead time (up to 30 - shorter is better, 2 points lost per week; 15 if not reported) and service level (Emergency supply 20, Expedited 14, Standard 8). Levels: 85+ Highly reliable | 65-84 Reliable | 45-64 Standard | below 45 Variable. Whether this dimension matters for you depends on your specific project.
—Not disclosed
Documentation iCounts documents in the profile vault at 5 points each, capped at 35, plus flags for a Certificate of Analysis (15), validation packages (15), DMF (10), CEP (10) and a TSE/BSE statement (5). Levels: 80+ Full documentation | 60-79 Strong documentation | 40-59 Established | below 40 Basic. Whether this dimension matters for you depends on your specific project.
0Basic
Regulatory iCounts supported regulatory regions at 5 points each capped at 30, the share of on-platform audits with a clean outcome (no action, NAI or pass) worth up to 30 (15 if no audits yet), FDA inspection history (20 if inspected, 10 if only registered) and QMS maturity (Validated 20, Established 12, Basic 4). Levels: 80+ Inspection-proven | 60-79 Strong regulatory | 40-59 Established | below 40 Developing. Whether this dimension matters for you depends on your specific project.
30Developing
Breadth iCounts product categories at 7 points each capped at 35, catalog size at 3 points per listed product capped at 30, modalities served at 4 each capped at 20, plus 8 for sterile-grade and 7 for GMP-grade offerings. Levels: 80+ Broad portfolio | 60-79 Multi-category | 40-59 Focused | below 40 Specialist. Whether this dimension matters for you depends on your specific project.
32Specialist