Pensa is very excited to announce its recent partnership with NextDocs. NextDocs provides an integrated solution that meets the needs of today's business. It is an easy to use, web-based enterprise software solution that enables organizations to comply with FDA 21 CFR 11, GMP, GLP, GCP, and other regulations and industry standards .

PENSA uses Quality Engineering methods
PENSA Technology Solutions Inc. will deliver innovative Information Technology solutions that meet or exceed worldwide regulatory and quality standards.

PENSA specializes in computer system validation projects
Specializing in computer system validation projects for pharmaceutical, medical device and biotechnology manufacturers, PENSA can guide your Life Sciences company toward meeting worldwide regulatory compliance. PENSA's validation products and services include 21 CFR Part 11 assessments, quality audits, creating/managing compliance documentation and validation training which follow cGMPs as put forth by the FDA.

PENSA's extensive in-house experience makes the difference
PENSA is knowledgeable in compliance projects for ERP, LIMs, CMS, DMS, MES and any process or lab equipment.