The pharmaceutical industry is an indispensable pillar of modern healthcare, relentlessly dedicated to advancing medical science, alleviating human suffering, and enhancing the quality of life. With a profound commitment to […]
Pharma ERP: Driving Efficiency Read More »
Manufacturing medicine is one of the most highly regulated businesses, with rapid changes happening every once in a while. Pharmaceutical companies must be adaptive to these changes and adequately follow
Cloud ERP software for the medical manufacturing industry Read More »
European companies must be alert to a number of specific risks that are unique to the pharma industry. Here we will look at seven deadly risks of the European pharmaceutical
The Hidden Risk of The European Pharma Industry Read More »
Despite a booming market, warehouse and storage productivity dropped 7.6% last year; much of this can be attributed to growing pains as companies increase warehouse capacity, embrace the new automation
3 Major Challenges for Pharmaceutical Warehousing & Distribution Read More »
This is a series of blogs about dealing with errors related to veterinary drugs and how to deal with these errors with the help of suitable manufacturing software. We publish
Veterinary Medication Error: What You Should Know in 2022 Read More »
To safeguard the health and welfare of animals, the FDA encourages veterinarians and animal owners to report adverse events associated with drugs or devices used in animals. We use this
Reporting Animal Drug and Device Side Effects and Product Problems Read More »
Drugs, according to the Federal Food, Drug and Cosmetic Act (the “Act”), are substances or preparations recognized in the official United States Pharmacopoeia, official Homeopathic Pharmacopoeia of the United States,
FDA’s Legal Marketing Status for Animal Drugs Read More »
A Five-Key Framework for Compliance in Pharma The challenge of continually meeting regulatory compliance standards and responding to continuous change can overwhelm pharmaceutical companies. Compliance champions know that policies are
A Five-Key Framework for Compliance in Pharma Read More »
In the world of food and drug compliance, penalties for non-compliance can be severe. The medical device regulations set forth in 21 CFR Part 820 can be difficult to follow.
Have you received an FDA 483 letter? If you are in the healthcare industry, chances are you have heard of the cGMP regulations and that the consequences for not adhering
Compliance Issues in the Pharmaceutical Industry – US And EU Read More »
