Quality Control

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.,

Quality Control Department Comprises

  • Central Quality Control laboratory with instruments, chemicals,in process quality control and microbiological facility.
  • Documentation
  • Control samples and stability chamber
  • Validation
  • Audits
  • Investigation
  • Reserve sample management

Documentation And Record System

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.

Quality Assurance

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

  • Qualification and approval of Vendors, Qualification of Facilities, Equipments, Utilities, & Analytical Instruments.
  • Validations of Process, Methods, Cleaning etc.,
  • Handling of Complaints, Deviations, Change controls, Product recalls.
  • Handling of audits by the Regulatory, Customers and IQAs
  • Documentation in line with regulatory guidelines
  • Providing trainings to the personnel.
  • QA related documentation such as preparation of MFR’s BMRs, DMF in line with regulatory requirements.

Our Quality Policy

We at Ravoos Laboratories Limited, committed to:

  • Achieve customer satisfaction by manufacturing & Marketing of Quality assured products.
  • Meeting all applicable legal & regulatory requirements.
  • Continually improving the effectiveness of our “Quality Management Systems” by involvement and training of our personnel.
  • Integrating “Quality, Environment, Health & Safety” in all our manufacturing process at all levels and ensuring that they are in integral part of our management systems.
  • Periodically reviewing this policy, so that it remains relevant and communicating it to all concerned.
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