Validation is one of critical part of Current Good Manufacturing Practice (cGMP)
and International Conference on Harmonisation (ICH) regulations. We offer validation
and qualification (IQ, OQ & PQ) consulting and services to bio-medical equipment
manufacturing and pharmaceuticals industries to comply with the following standards,
such as (ISO 13485 clause 7.5.2 and Code of Federal Regulations 21 CFR 820.70 and
820.75).
We also offer consulting and implementation services on 21 CFR part 58 Good Laboratory
Practices (GLP).
For additional information, please contact us: info@callabaccess.com.