Our Services
Validation Solutions for Regulated Industries
We provide structured validation methodologies including risk assessment, IQ/OQ/PQ execution, documentation control, and regulatory alignment to ensure systems and processes are audit-ready.
Computer System Validation(CSV & CSA)
CSV and SCA are the systematic process of verifying and assuring that any computer-based system or application performs and delivers
results as intended, while ensuring compliance with regulatory standards such as FDA 21 CFR Part 11, GxP, and EU Annex 11 throughout its
lifecycle.
Equipment Qualification And Process Validation
The Equipment Qualification is a process of ensuring and documenting that any equipment under GxP environment operates and
produces the consistent and reliable outputs.
Data Migration and Validation
Today’s data-driven landscape, efficient data migration and robust data qualification are crucial for ensuring continuity and compliance
in your operations.
Software Testing and Validation
In the evolving world of technology, ensuring software quality and compliance with regulatory standards is crucial, especially in regulated
industries such as pharmaceuticals, biotechnology, and healthcare.
Pharmaceutical Licensing Services
Pharmaceutical Licensing is a formal, legally binding agreement or process that allows one company (usually called the licensee) to use,
manufacture, market, or distribute a pharmaceutical product, technology, or intellectual property owned by another company (called the
licensor) under agreed terms and conditions