Your Projects, Greenfield or Brownfield are to be completed in strict time frame and you constrained with limited resources. Genugrity Pharma Services is of great to serve in such toughest times and in strict time frames. We are offering commissioning & qualification of facilities, equipment and utilities. Our ready available, time and again challenged solutions, protocols and experienced technicians serve your purpose.

Our services in facility commissioning and qualification include,
Design concept development, review and to give value additions to meet regulatory requirements.
Develop design basis and concept notes

Closely work with clients to develop quality validation protocols and reports. Our protocols include customized validation approaches and methodology with clearly defined, pre- determined acceptance criteria. We offer fast documentation turnaround and can schedule validation projects with short lead times to achieve a compliant system.

We use a pragmatic, integrated approach to commissioning and validation activities – ensuring sound documented compliance with cGMP for all our assignments. We offer full validation services associated with manufacturing projects and offer services to retrospectively validate existing manufacturing processes. We can assist you with the interpretation of regulations in determining the validation requirements, manage implementation of methodologies, and prepare necessary reports.

Our validation approach is based on current GMP, GLP, GAMP 5, ISO, and 21 CFR Part 11 regulations. Our experienced staff will ensure that protocols are written and executed according to user requirements, specifications, applicable regulations, and SOPs. We provide versatile services that include: Protocol Preparation, Execution and Final Report preparation.