The business environment of the pharmaceutical industry is constantly evolving, empowering consumers to access unlimited information. The digital revolution has caused a drastic shift of power from business heads to […]
Reasons to Move Your Pharmaceutical Business to the Cloud Read More »
The development of COVID-19, a modified version of the live attenuated influenza vaccine (LAIV), will have a considerable effect on the pharmaceutical manufacturing industry; however, the influenza pandemic has provided
Why Quality Management in the Pharmaceutical Industry is Important Read More »
A medication error is an undesirable, unintended act in a drug administration process such as ordering, transcribing, dispensing, or administering a drug product. Communication between the veterinarian and the client
Ways to Prevent Medication Errors and Accidental Medication Exposures in Your Animals Read More »
In this article, you’ll learn about issues the veterinary industry struggles with. And how Acu Process Manufacturing Software helps deal with inventory tracking, Compliance, legal regulations, drug formulations, and many
Vitamin D toxicity in dogs is a notifiable condition. Read More »
Developing new drugs is a challenging and rewarding process. As a result of the vigilance of the U.S. Food and Drug Administration, consumers enjoy access to the safest and most
Development and Approval Process for Drugs Read More »
This is the second blog series on the FDA’s drugs reviews process; here, visit for part 01. Explore here: Before continuing, let me give you a brief introduction. Tayan Solution
Understanding Drug Review Processes (PART 02) Read More »
Note; Before we proceed, a Brief introduction, Tayana Solutions provides ERP for the process manufacturing industry. Acu Process Manufacturing is an ERP that manages the process manufacturing business smoothly. Along
Biotech companies developing drugs for the first time often face difficulties in creating formulations of the drug that will be safe for humans. Formulation development is not only important in
Do You Really Know FDA Medical Device has 3 Classes to Ensure Safety for Patients? The Food and Drug Administration (FDA) is setting up a system so that those who
Differences between FDA Medical Device Classes Read More »
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 »
