Having Facility Compliance Issues?
Want to Quickly Regain Control?
Join Our Facility Compliance Fast-Track Program!
3 Outstanding Benefits of our Facility Compliance Fast-Track Program
Tailored cGMP compliance modules available 24/7 + live workshops.
All the document templates you need for an audit ready Quality System.
Expert support through the program to rapidly increase compliance.
6 Reasons to Join the Rapid Response Remediation Program
Risk-Based Prioritization
The program uses ICH Q9-aligned risk assessment tools to help you identify, score, and prioritize risks, so you’re focusing resources where they will have the greatest impact on product quality and compliance.
Expert Support
Work with industry-leading consultants who bring experience from sterile, non-sterile, and ATMP facilities. Pharmalliance has supported clients during and after FDA, EMA, and MHRA inspections.
Rapid Deployment
Get immediate access to a full suite of customizable templates, risk assessments, Policies, Pland, Procedures, and trackers, eliminating delays and giving your team a clear starting point from day one.
Coverage Across GMP Systems
​Address compliance gaps across facilities, utilities, equipment, contamination control, training, and quality systems. This ensures a holistic and sustainable remediation approach protecting your site and patients.
Quality Remediation Plan (QRP)
​Develop a site-approved, audit-ready QRP that outlines your entire remediation roadmap, complete with timelines, responsibilities, and verification steps—ready to present to regulators.
Saves Time, Resources, and Cost
​Avoid the cost of delays, repeat findings, and trial-and-error fixes. Our program can save your site up to €200,000 and six months of effort compared to traditional consultant-led approaches.
Some of our happy clients
