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 …
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 …
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, …
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 …
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 »
