ISO 13485:2016 Medical devices Quality management systems Requirements for regulatory purposes
Operational Qualification
CSV Computer System Validation
QSR Quality System Regulations 21 CFR part 211
Software
ECA Environmental Controlled Areas
Outsourcing
Lean Manufacturing
Installation Qualification
Kaye LTR140 Temperature bath
Consulting
Validation Consulting Services in Puerto Rico 2018
FDA inspections audits
Dry Heat and Steam Sterilization
FDA cGMP and Reguiatory Compliance 21 CFR Part 820
Pharmaceutical Validation Experts
Hiring Full time Engineers immediately
Quality Assurance
EO
Health Care
ISO 14666 Cleanroom Certifications
GE KAYE Validator 2000 rental leasing
Gamma
Dataloggers rental leasing
Lean Six Sigma
Commissioning and decommissioning
Medical