||Validation and Pharmaceutical
V Force assists clients with research, development, validation,GMP reviews of new facility design, evaluation of existing operations, cGMP audits of facilities/suppliers and FDA regulatory consulting. We develop validation master plans, plan and schedule validation projects and prepare and execute IQ, OQ and PQ protocols. In addition, we provide GMP training and certification and pre-FDA plant inspections.We have developed and proven a methodology for efficient integration of commissioning and validation activities in accordance with ISPE guidelines.
V Force provides adequate validation and verification services to ensure that our client gets the best value from the software applications. This service has been proven to be most effective in reducing the risk and providing long term benefit from the quality application.Our specialists have gained cutting edge validation experience in areas such as process, cleaning, equipment, analytical and software/automation..
We offer wider range of Bio-statistical, Statistical programming and Data management services according to the needs of industry.
The highlights of the services and areas
- Regulatory compliances
- Medical software
- Functional specification
- GLP & GMP Method Development, Validation and Remediation
- UV Visible Spectroscopy
- HPLC, GC, IC and GPC Analysis
- Software application validations
- Pharmaceutical Data Auditing and Consulting
- LC/MS/MS Analysis
- GC/MS Analysis
- Software Requirements Specification
- Quality Control and Assurance (QA & QC) Testing Services.
- Validation (drug manufacture)
- Software versions and patches.