White Papers

White Paper: An Executive Guide to Pharmaceutical Manufacturing Efficiency and the Effect of Environmental Legislation

Solvent recovery offers simplified, low-risk method to reduce carbon footprint, shielding manufacturers from adverse effects of pending environmental regulations.

Press Releases | Posted July 8, 2010

White Paper: CERAM’s New White Paper Analyzes Cleanliness Validation

CERAM, an independent global expert in materials testing, analysis and consultancy for the medical devices sector, has published a white paper on cleanliness and cleaning process validation.

Press Releases | Posted July 8, 2010

White Paper: Vision Inspection Protects Your Brand’s Good Reputation

METTLER TOLEDO CI-Vision Introduces a White Paper on Label Mix-up Prevention.

Press Releases | Posted July 7, 2010

White Paper: Package validation requirements

Read this white paper for medical devices and combinatory products that provides insight on the general requirements in a microbiological and physical testing program.

| Posted July 30, 2009

White Paper: OEE secrets: What pharma can learn from beverage

White paper from Hartness shows how new types of accumulation technologies perfected in beverage can wring maximum efficiency out of pharmaceutical packaging lines.

Packaging Line Efficiency | Posted March 29, 2009

White Paper: Ensure problem-free printing for pharmaceutical blister packs and pouches

Pharmaceutical companies want and need to focus on their core business. Inline printing of blister packs and pouches is a necessity that has been imposed upon them, and they seek problem-free printing solutions that can help enhance production and maximize profitability. Read about how to achieve this without roadblocks in this White Paper from Griffin-Rutgers.

Coding, marking, printing | Posted March 29, 2009

White Paper: 7 Essentials for Successful Medical Package Design

Individuals responsible for medical packaging system design and validation are required to provide a safe and effective packaging system that can deliver the enclosed product to the end-user without incurring defect or risk to patient safety.

Medical devices | Posted March 29, 2009

White Paper: Three Testing Tips for Medical Device Packages

Sterile Medical device package testing is a requirement for compliance to ISO 11607 “Packaging for Terminally Sterilized Medical Devices”, Part 1: Requirements for materials, sterile barrier systems and packaging systems and Part 2: Validation requirements for forming, sealing and assembly processes.

Medical devices | Posted March 29, 2009

White Paper: Free ARC brief on the pharmaceutical industry in transition

Modern packaging technology and controls will play an increasingly important role in manufacturing performance and regulatory compliance in the pharmaceutical industry. Read this forecast now!

Pharmaceuticals and biologics | Posted March 27, 2009

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