Documentation & QS

By understanding the needs of your business and how you currently manage the activity flow, REDWING’s consultants can documentation that matches your needs and increases the efficiency of your business We have expertise sources from various industry in following areas.

1. SOP / manual preparation
2. DMF compilation for API / intermediate as per latest regulatory norms
3. Equipment & instrument qualifications 
3. FDA registration.
4. Process or utility system Validation 

ISO 9001:2008

Good quality does not cost-it pays. But many companies do not recognize it as they do not know how much things cost due to missing cost calculation in many areas. And that is the reason why it usually takes a long time for them to think their processes over and to implement simple measures assuring reduction in cost of delivering customer satisfaction. The latest one does not have to be as high as the cost of materials!

Our multi-cultural team includes technicians and experts whose experiences extend beyond routine quality inspection, laboratory testing, auditing and technical advisory. As a niche player, we excel at supporting both flexible and structured quality workflow.

Good Manufacturing Practices [GMP]

We serve Small and Medium Enterprises, as well as large Pharmaceutical organizations and laboratories.
Through our Quality Assurance offering, we assist companies in identifying opportunities and deriving actions to improve their processes, sales conversion , customer satisfaction and regulatory compliance Promoted by seasoned Pharmaceutical professionals having rich experience in all aspects of Pharmaceutical and laboratory operations. We serve Small and Medium Enterprises, as well as large Pharmaceutical organizations and laboratories. Through our Quality Assurance offering, we assist companies in identifying opportunities and deriving actions to improve their processes, sales conversion , customer satisfaction and regulatory compliance

  • WHO
  • India FDA
  • ICH
  • EU-GMP