3 min read
Under Directive 98/69/EC (IVDD), it was common practice for in vitro diagnostic medical devices to be placed on the European market under contractual agreements between a Private Label Manufacturer (PLM) and an Original Equipment Manufacturer (OEM)....
Read More
5 min read
How do regulatory requirements within the medical device industry impact a database build? What are the important items to be aware of? In this blog,...
4 min read
Nicolas Borenstein, DVM, Ph.D. Co-President, Preclinical Services “We are not a veterinary clinic and our primary mission is indeed to validate...
5 min read
The most expensive study is one you have to repeat Good laboratory practice (GLP) studies are an essential component to medical product development...
2 min read
Extending Patient Lifespan with LifeSTEM What is Glioblastoma? Gliomas are brain tumors that come in multiple forms ranging from low-grade, benign...
4 min read
When it comes to meeting deadlines and continuing to receive investments, the timely review of your GLP preclinical final report is very important....
3 min read
Accelerate Your Product Development Timeline One of the biggest timeline impacts in any development program is getting the product to work. Our...
6 min read
ECMO Vs. VAD Ventricular assist device (VAD) and extracorporeal membrane oxygenation (ECMO) are two similar temporary techniques to bridge cardiac...
5 min read
When a medical product innovator has reached the point at which preclinical research is necessary to achieve the next milestone, they have already...
3 min read
Postpartum hemorrhage (PPH) remains a significant global health concern as the leading cause of maternal mortality worldwide. According to the World...
