article thumbnail

The Role of ERP in the Pharmaceutical Industry

Navigator SAP

The pharmaceutical industry has been transformed in recent years by pressure from intensely competitive markets and the need to comply with new regulations that mandate the highest quality standards across all processes. As such, cloud ERP is critical for pharmaceutical operations today given this environment.

article thumbnail

Maintaining Quality As a Scaling Contract Manufacturer

Navigator SAP

It’s an uphill task for Contract Development and Manufacturer Organizations (CDMOs) to ensure product quality at the rapid pace demanded by customers, especially when they must deal with safety, control, and regulatory regimes in fields such as pharmaceuticals, biotech, and other areas of the life sciences.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Trending Sources

article thumbnail

CDMOs, CMOs and CROs: What's the Difference?

Navigator SAP

The pharmaceutical industry has undergone significant evolution within the past 15 years. Recently, biopharmaceutical companies have become increasingly reliant on outsourced contract services for various elements of their value chain.

article thumbnail

What is FDA Software Validation?

Navigator SAP

When a pen is manufactured incorrectly or suffers from shoddy inputs, a consumer just pulls out a different pen. When a life sciences product deviates from specs, be it a pharmaceutical or medical device, public health is affected and the defect might not even be readily observable. The life sciences are not like pens or bras.

article thumbnail

Why Cloud ERP is a Great Fit for CDMOs

Navigator SAP

Contract development and manufacturing organizations (CDMOs) face unique challenges. They’re outsourced to handle drug and therapy development as well as to manufacture pharmaceutical, nutraceutical, and biological materials.

article thumbnail

Indian drug manufacturers benefit from Big Pharma interest beyond China

CFO News

China has for nearly 20 years been the preferred location for a range of pharmaceutical research and manufacturing services due to the low cost and speed offered by contract drugmakers there.

article thumbnail

FDA and GxP Validation for SAP Business ByDesign ERP

Navigator SAP

Following good manufacturing practice (GMP) guidelines help businesses run more efficiently and ensure that product quality and consistency are maintained. The processes that life sciences businesses follow must be validated in line with FDA regulations 21 CFR.

SAP 212