Fill / Finish Design

Improve the total performance of your fill-finish products

Understanding the key drivers of your business – technology and regulatory requirements – is critical when designing or upgrading sterile and aseptic filling suites.

As a recognized leader in the design of biopharmaceutical manufacturing facilities, CRB can provide expertise in process design and scale-up, assurance, validation, and regulatory support for virtually any dosage form.

Sterile Products

  • Component Preparation
  • Formulation
  • Filling
  • Lyophilization
  • Capping, Sealing
  • Terminal Sterilization
  • Inspection
  • Labeling
  • Coding
  • Vision Systems
  • Packaging

Non-Sterile Products

  • Milling/Blending
  • Weighing
  • Granulation
  • Fluid Bed Processing
  • Tablet Compression
  • Coating
  • Filling (Bottles, Tubes)
  • Capping
  • Induction Sealing
  • Labeling
  • Coding
  • Vision Systems
  • Packaging

CRB understands the daily challenges in manufacturing and moving product through your facility.

  • People, Material and Equipment Flows
  • Minimize Cross-Contamination, Mix-Ups and Errors
  • Delivering Industry-Leading Engineering Solutions
  • Cost-Effective, Validatable Facility
  • Compliant with Governing Codes, Laws, Regulations and Your Needs

Innovative layout and line design starts with CRB listening to you and offering a customized approach that best satisfies your specific business needs:

  • Application and Use of Barrier Isolation
  • Traditional Filling Suites
  • Secondary and Tertiary Packaging Lines
  • Practical and Reliable Results
  • Validation Oriented Documentation