GMP Documentation Library

cGMP documentation is a highly-specialized and detail-oriented process.

With constantly evolving documentation requirements from the FDA and other regulatory bodies, it’s a real challenge to keep your team up to date.

That’s where Azzur Group comes in.

With decades of on-site experience, as well as strong relationships with regulatory bodies, our GMP engineers and consultants have their fingertips on the pulse of change in the industry.  

Our current program offerings include:

  • Commissioning, Qualification, and Validation
  • Calibration & Maintenance
  • Quality Management System
  • Equipment-Specific Templates
  • Computer System Validation
  • Medical Device
  • Materials Management
  • Part 11 & Data Integrity
  • Quality Control
  • Facilities Operations

We save you time, money, and worry when it comes to critical documentation.

Your time is valuable. That’s why we offer customizable policies, SOPs, forms, plans and protocols to serve the needs of all your GMP programs.

Value
Because it’s a price-fixed option, Azzur’s GMP Documentation Library eliminates ongoing costs and risk associated with technical writing on a time and materials basis.
Expertise
Azzur’s GMP Documentation Library has been developed and consistently updated by internal subject matter experts (SMEs) over the course of decades, giving you access to collective knowledge at a fraction of the price.
Time
Azzur’s GMP Documentation saves time through the use of our master templates, eliminating 80% of delivery time.
Delivery
Delivery of the GMP Documentation Library is professionally managed to ensure facilitative review is followed, with SME access, as needed. Azzur ensures final documentation is integrated within your formal documentation management system and training systems.
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