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KQE-WCG - Home
Kindsvater Quality Engineering & Wisdahl Consulting Group: consultants on ISO 13485, ISO 9001, FDA, Health Canada, CE Mark
quality
study
risk management
clinical
clearance
device
FDA
quality assurance
regulatory
Medical devices
recall
risk analysis
clinical trial
pma
regulatory affairs
eec
mdr
quality systems
CE Mark
MDD
clinical study
hazard analysis
Health Canada
510 k
510k
design control
clinicals
design controls
premarket approval
problem reporting
investigational device
www.ra-qa.com - 2009-02-06
Medical Device Regulatory Advisors - Regulatory and Quality System Specialists
Regulatory approval and quality system consulting services for the device, drug, and biomedical manufacturing industries.
agent
medical
consultant
healthcare
drug
pharmaceutical
clinical
biotechnology
biotech
device
FDA
regulations
regulatory
biomedical
IDE
NDA
IND
in vitro
ANDA
IVD
quality systems
food and drug administration
510 k
510K
fda approval
adverse event
fda consultant
us agent
design controls
device advice
united states agent
www.deviceadvice.com - 2009-02-12
QA/RA Compliance Connection, Inc.
QA/RA Compliance Connection, Inc. Quality Assurance and Regulatory Affairs consulting services and training company. Provide asssessment, gap analysis, ...
management
training
florida
consulting
development
company
quality
system
industry
manufacturing
tampa
assessment
compliance
ISO
assurance
implementation
ISO 9001
Inclusive
specializing
regulatory
quality control
affairs
9001
ISO 13485
gap analysis
CE Mark
Design Controls
EN 46000
ISO 17025 calibration
FDA QSR 21 CFR 820
Medical Device Directive 93
www.qaracc.com - 2009-02-07
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