QMS PHARMA CONSULTANCY
QMS Pharma Consultancy is your single source for expert insights pertaining to technical, quality compliance, and regulatory assistance throughout the product lifecycle, .
We are Professional Agency
QMS Pharma Consultancy is an independent firm specializing in Quality Management Systems, GMP, and GLP for finished products, intermediates, excipients, and APIs. We aim to create transparent, integrated, and compliant systems that support every stage of your business from product development to launch and beyond.
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If you can’t describe what you are doing as a process , you don’t know what you’re doing
We provide best services for your business
Troubleshooting Quality Issues
Technology is advancing rapidly and its application in the production of pharmaceuticals is changing all the time.
Quality Systems for Pharmaceutical Manufacturers
If you need world-class quality systems in place at your facility, QMS Pharma consultancy can help you design.
Regulatory compliance auditing
If you want to make certain your facilities and procedures are compliant with regulations like USFDA,EU GMP,MHRA,TGA,WHO and ANVISA. We conduct vendor and third party audits.
Qualification and Validation
If your infrastructure doesn’t meet regulatory standards, or isn’t robustly validated at each stage. We support to area and equipment qualifications.
Capital & Project Management
expert project management is crucial to bringing your new pharmaceutical product to market.
Quality and Regulatory Management
QMS Pharma Consultancy ensures regulatory compliance, supporting LIMS, eDMS, QMS software, resource management, and validations.