Resources & Inspiration
Building A Fit for Purpose Quality System
As we celebrate Nd’s achievement of obtaining ISO 9001:2015 certification, we are delighted to share our success stories regarding our Quality Management System (QMS) and
Challenges of Implementing Digital Solutions in the Pharmaceutical & Biopharma Space
We have looked at digital transformation in the form of accelerating Quality 4.0 in the previous article. Now, we will take a look into some
No deviation and DNAlytics partner to monitor and enhance pharma manufacturing processes
No deviation, a patient-centric solution provider for the pharmaceutical industry is pleased to announce its partnership with DNAlytics, a consultancy tech company developing innovative data-driven
Digital Transformation: Accelerating Quality 4.0 Through Connected Life Sciences
As the pharma industry evolves, digital transformation is slowly gaining importance. Digital transformation can affect many parts of the lifecycle of a drug. However, it
The Future of Pharmaceutical Inspections
At the recently held ISPE Singapore Affiliate Conference & Exhibition 2022, Dr Joey Gouws, the Team Lead of Inspections of the World Health Organization Prequalification
The Role of the World Health Organization (WHO) in Global Regulatory
How much do you know about WHO and the role it plays in providing access to medicines and health products? As shared by Dr Joey
Preventing cross-contamination in the pharmaceutical industry
Often on projects in the pharmaceutical industry, we are asked various questions regarding cross-contamination prevention. It could be a greenfield project for a multi-products and
Digitisation in pharma CQV: How does it help?
In the regulated pharma environment, “what is not documented is not done”. While many organisations in the pharma industry have been using paper to document
