The Compliance Group in Wilmington, DE, US (United States)

The Cleaning Validation Process The current good manufacturing practices recognize that the cleaning process is a critical issue to assuring product quality. Working in a multi-product facility can be a complex task when developing a cleaning validation process. 

21 CFR Part 210/211 - Good Manufacturing Practices; 21 CFR Part 820 - Medical Device Regulations; 21 CFR Part 11 - Electronic Signatures and Electronic Records 

Who We Are In business since 1996, with offices in: New Jersey -- 48 Broad St., Suite 201 Red Bank, NJ 07701 Maryland -- Pilot Office as of Jan 2007 Rockville, MD The Compliance Group, Inc. has a national presence. 

The Compliance Group, Inc. Contact Information Home Company Profile Management Consulting Audits / Assessments Engineering / Commissioning Quality Systems white spacer clear image dotted line arrow off Engineering / Commissioning / Maintenance clear image dotted line arrow off Validation and GMP 

Engineering / Commissioning / Maintenance Supporting the Validation Process is important and needs programs that may include a series of procedures to coordinate a process. Our compliance consultants are specialized in many areas and have developed many programs for implementation.