"Remediating Your Consent Decree, Warning Letter, Multi-483s and Quality System Challenges Right First Time and Fast By Spending Less"
We are Consent Decree, Warning Letter, 483, Quality System and regulatory compliance remediation medical device and pharmaceutical industry consultants with 30+ yrs of impressive, verifiable accomplishments in US, Europe, Japan, China, India & Mexico.
Company-wide risk mitigation strategy development, implementation and management
Complete Quality System/ Lean Six Sigma (LSS) remediation/ development/ implementation
Software systems validation
Companies with Consent Decree, Seizure, Market Withdrawal/Recall, Warning Letter, Multi483 FDA violations are typically under severe distress due to regulatory non-compliance. We have helped client companies over 30+ years to properly and quickly manage their risk by remediating found regulatory compliance deficiencies Right First Time (RFT) by spending less..
Clients hire us because they believe we would give them the best chance to successfully complete their project RFT by spending less. Apparently, our collaborators/clients believe as we do that we are a great consulting company.
Contact Always Excellence(tm)403 Christie Court, Stewartsville, NJ 08886 | 908-827-1715