The Quality control department at Ravoos Laboratories Limited follows GLP recommendations and fulfills local and international regulatory requirements.
Our Laboratories are well equipped with advanced qualified analytical instruments such as HPLC’s, UV’s, GC’s Dissolution apparatus, Digital Karl Fisher Moisture analyzers etc.,
Our Microbial Laboratory is equipped with Laminar Air Flow Apparatus, provided with BOD incubators, Colony counters etc.
Roles & Responsibilities of our QC are conducting of physiochemical and microbial analysis of Raw, Packing materials and In-process, finished products as per the pharmacopeia and In-house specifications and methods.
Developing RM, PM & FP analytical methods and Method validations.
Handling Stability activities, Control samples, Investigation and Documentation of OOS etc.
Documentation such as Preparation of Specifications, Method of analysis, Analytical worksheets, Certificate of Analysis etc.,
Each batch processed under controlled series of in process checks which are recorded in batch production record. On completion of any batch the samples are checked by quality control labs & released for finished goods transfer. All necessary details are recorded in batch production record. This batch is transferred to finished goods godown for further distribution.
The Quality Assurance department ensures that the products are manufactured and analyzed in line with the requirements of GMP and ISO 9001:2008 Quality Management Systems.
Roles & Responsibilities of our QA are
We at Ravoos Laboratories Limited, committed to: