When it comes to regulatory intelligence, change is the only constant.
Yet keeping up is more complicated than it seems for many organizations, especially in pharmaceutical industry.
Read this article to explore what businesses need to know about regulatory intelligence to stay ahead of trends.
Steam is used to power many processes in the energy sector, such as power turbines and sterilize equipment in the medical industry. This highly flexible gas comes in two forms: pure steam or clean steam which is generated from completely purified water. This article will explain the differences between pure and clean steam, and why each type is essential.
Smart Quality is not just a catchphrase that will soon be trendy – it’s a revolution that will reshape what quality and service can do. This article will explain more about the Smart Quality framework and how it can help your companies move from a compliance-based culture to a quality-focused one.
In this webinar, you will gain a thorough background in all the important regulatory changes and updates that are going on right now. This will allow you to make informed choices about what regulations impact your operations and need- to- have specific regulatory actions, operational changes, and QMS updates.
Although track and trace programs are important to provide drug safety and prevent counterfeiting, the regulations for these programs can be very complex. This article will explore the importance of these programs and discuss common challenges in implementing them.
This webinar gives you the tips and common mistakes you need to consider to get a world-class and airtight life science supply chain in place.
FDA has developed Quality Management Maturity Program (QMM) for drug manufacturers to have consistent, reliable, and robust business processes to achieve quality objectives and promote continual improvement. This article will explain the meaning of QMM and why do pharma companies need to develop a QMM program.
By attending this webinar you will understand the benefits of evolving from compliance-only solutions to the Smart Quality model.
Pharmaceutical companies must be compliant with all applicable regulations and produce high-quality products. But these systems are often complicated to manage. This article explains the different compliance requirements that pharmaceutical companies must meet and how products are evaluated for quality.
There are several terms in regulated temperature control in pharma. This article will explain the meanings and the terms ambient, room temperature, and cold chain.
Download our free Ultimate FMEA Guide, which is dedicated to GMP and pharma professionals.
This extensive yet simplified guide to Failure Mode and Effects Analysis (FMEA) will help you master one of the most vital instruments in your risk management toolbox.
