Five Questions to Ask when Prioritizing GMP Audits
Five Questions to Ask when Prioritizing GMP Audits By: Greg
Advancing Your Pharmaceutical Product Through Development
Our Services
Eastlake Quality Consulting (EQC) is dedicated to helping your company maintain compliance with good manufacturing practice (GMP) standards and regulations. EQC develops policies and procedures tailored to your specific needs, and provides training for your staff. EQC also offers auditing services to ensure that your operations are always in compliance.
The EQC Difference
Data-Driven Decision Making
Regulatory agencies require decisions made in the development of a drug candidate be based on hard data rather than on intuition or guesswork.
Combining Science with Compliance
Science and compliance aren't distinct. They must work together to overcome tough challenges and provide patients much-needed supplies.
Product Lifecycle Quality Management
As pharmaceutical goods progress from start to finish, regulatory expectations for manufacturing and testing controls and quality systems increase.
Resources
De-Bunking the Myth – “21 CFR Part 11 is more of a Suggestion than a Requirement.”
De-Bunking the Myth – “21 CFR Part 11 is more
De-Bunking the Myth – “All Contract Manufacturers Have Great Customer Service”
De-Bunking the Myth: All Contract Manufacturers Have Great Customer Service
GMP Term of the Week – Performed by / Verified By
GMP Term of the Week – Performed By / Verified
