Activities of NML

• Test and analyze the quality of drug as empowered according to the Drug Act 1978. 
• Analysis of regulatory drug samples submitted by DDA collected during the process of inspection and investigation by authorized inspectors and public complaint sample submitted by DDA. 
• Analytical Method Validation of Non-Pharmacopoeial Products. 
• Post market intervention and quality monitoring of drugs. 
• Analysis of drug from Government, non-government and private organizations. 
• Providing technical service in pharmaceutical field. 
• Facilitates different institutions for observation cum interaction. 
• GLP Audit of private analytical laboratory and quality control laboratories of pharmaceutical industries. 
  • Check and evaluate the standard of drug testing laboratories in the country as per “WHO good practices for pharmaceutical quality control laboratories” and “WHO good practices for pharmaceutical microbiology laboratories” 
  • Conduct training on Good Laboratory Practices (GLP) for national pharmaceutical industries and laboratories. 
• Participation in the proficiency testing (PT)/Inter Laboratory Comparison (ILC). 
• Biological products lot release certification. 
• Research and Development