January - 2018 4/6

EUDR Compliance: Chemical Cleaning Supply Chains

Clinical Research is one of the most critical area in Pharmaceutical industry, which contributes greatly to the effective development of...

Cosmetics Regulatory Intelligence Cosmetics regulations vary from region to region. While some countries demand registration of cosmetic...

Nowadays, most pharmaceutical companies, research institutes and life-science suppliers rely on contract manufacturers to meet their...

The Life Sciences market is growing and is expected to reach US$ 4,200 Million by the end of 2024. At the same time, the world is turning...

Global Regulatory Services Freyr’s Scientific and Medical writing team has proven expertise in delivering world-class Regulatory and...

Freyr Artwork Pack Management CoE provides innovative, cost effective, creative graphic design & artwork services to support new product...

Study data is information about a person in a clinical trial. It includes demographic information, details of medical treatment,...

Drug Master File (DMF) is a file that is used to provide confidential and detailed information about facilities, and processes used in...

Regulatory Product Submission (RPS) is an HL7 standard introduced by the US Food and Drug Administration (FDA Submission). As defined in...

As per the United States Food and Drug Administration (USFDA) norms, adopting technology, its processing, managing, labeling and details...