Quality Control :

For a better quality of life, we follow stringent quality norms. Our medicines adhere to internationally recognized pharmaceuticals standards. Our quality control is headed by our director Dr.Ulhas Ganu, who himself is a research scientist in Cancer research, with an experience of 28 years of research activities. Dr.Ganu himself along with the other faculty members have set up a stringent quality control system for raw materials, packing materials, in process as well as final products from the first point of receipt to the final disposal of finished formulation.

We have a modern and well-equipped Quality Control (QC) laboratory with latest analytical instruments like HPLC, HPTLC, GC-MS, LC-MS/MS, FTIR sterility test unit, Karl Fischer titrator etc. Quality up-gradation of our products is a regular developmental feature of the QC department, resulting into achieving products of highest international standards.

Our QC department is equipped with almost all the in-house testing facilities for ensuring world class quality of medicines. It is also having adequate, competent technical staff to carry out the manufacturing operation and analysis. It has all necessary instruments for analysis of API, finished products, packaging and related materials used.

Stringent quality control systems and a batch to batch quality checks are a part of quality process at Zuvius Lifesciences and is a part of or long term approach, adding value to our quality competence. Morever, regular in-process inspection and analysis is carried out to ensure that the product is manufactured as per the S.O.P. and B.M.R. cGMP is being adhered to and product conforms to the specification.


The quality assurance department is responsible for preparing, issuing and updating quality policy, maintaining and controlling all documents as per the respective SOP.

The QC department’s span of responsibility includes:

• RM/PM analysis which includes approval / rejection of raw materials.
• Finished Products analysis and maintaining the BMR’s, DMF,etc.
• In-process Checks which includes in process testing as per the respective SOP.  
• Stability Studies
  
  

The QC activities are managed through four sections:

• Instrumental Analysis and Finished Products
• Wet Analysis Laboratory
• Microbiological Testing Laboratory
• Packaging Material -Testing Laboratory