Pharmaceutical - Lean Manufacturing consulting services

When benchmarked against other similar industries, such as the food industry, drug companies frequently come up far short in critical business benchmarks.

Typically, non GMP critical indicators such as stock turnover, manufacturing cycle times tool or machine changeover times and QC release times are well short of these benchmarks.

There is usually no GMP impediment to embrace the best from other industries. Tools and techniques successfully used in other industries, can be successfully applied to pharmaceutical facilities. The difficulty lies in doing this in conjunction with GMP and other Quality guidelines.

PharmOut offers a range of lean manufacturing and other process improvement consulting services to assist pharmaceutical manufacturers in improving their processes and be GMP-compliant.

PharmOut will provide the Pharma-aware resources and skills to implement your cost reduction projects, whilst you concentrate on the core business. 

Lean Manufacturing

Lean Manufacturing focuses on eliminating waste or non value adding activities in manufacturing processes. PharmOut Consultants have extensive experience in introducing Improvement Programs in a manufacturing / pharmaceutical environment.

Description

Lean Manufacturing is an amalgamation of Just in Time, Kanban and Total Quality ideas leading towards zero paper, zero inventory, zero downtime, zero defects, and zero delays in design, manufacture and distribution and all whilst ensuring Quality system compliance.

Example

One pharmaceutical company identified laboratory testing as a key bottleneck in their manufacturing process. Stock sat in the in process warehouse for up to 3 weeks, waiting for the lab results.

By investing in modern instrumentation, and complying with the FDA's, Process Analytical Technology (PAT) philosophy, the company was able to reduce this in-progress time by 2 ½ weeks.

To learn more:

Please contact us to discuss your needs.

 

Validation, GMP, Consultants quality management systems GMP, GLP training validation jobs TGA, Medsafe, FDA
 
Validation Master Plans

Validation

Validation Outsourcing

Computer System Validation

GAMP 5

Part 11 / Annexe 11 Checklist

Validation Consultants

Validation Contractors

Autoclave Validation

Project Management

GMP Compliance

What is new?

QA Outsourcing

APVMA Regulations

GMP Compliance

Risk Management

Drug / Medical Device Registration

Pre-clinical Consulting

Regulatory Affairs

Medical Device Consultants

Lean Pharma

Lean Consulting

Continuous Improvement

What is 5 S?

 

Home | About UsContact  | Downloads | Search | Blog