![zifo - software as a medical device companies](https://dev.zifornd.com/wp-content/uploads/2022/02/software-as-medical-device.jpg)
SaMD validation strategy, IQ, OQ, PQ development and qualification, software validation execution and regulatory reporting across SaMD regulations
![](https://dev.zifornd.com/wp-content/uploads/2022/01/quality-compliance.jpg)
New quality system design/delivery/maintenance, auditing against regional regulatory guidelines (21CFRpart11, GLP, GMP, GCP, GAMP5), quality system audit and recommendations, quality system best practice adoption
![](https://dev.zifornd.com/wp-content/uploads/2022/02/lab-instrument-validation.jpg)
Instrument validation strategy, IQ, OQ, PQ qualification, risk-based approaches, execution and reporting across 21 CFR part 11, GLP, GMP, GAMP for all analytical instrument hardware platforms
![](https://dev.zifornd.com/wp-content/uploads/2022/02/computer-system-validation-csv.jpg)
CSV validation strategy, IQ, OQ, PQ development and qualification, risk-based validation, execution and reporting across 21 CFR part 11, GLP, GMP, GAMP for all lab software platforms e.g. CDS, EDC, ELN, LIMS, in the cloud and on-prem