Building the Pharmaceutical Factory of the Future

Individuals take for granted everyday interactions with well-designed products and devices that save both time and aggravation. Well-designed products can eliminate overall confusion for the user. Every day, more medical devices are designed for portability and at home monitoring. A major initiative in the medical device industry is to reduce the workload on our already overworked medical professionals. Medical device manufacturers must consider countless items when designing and manufacturing their final product, but unfortunately, connectors usually take a back seat to other more engaging topics. Nicomatic has relationships with many of the top medical device manufacturers to help them determine the best connector solution for their specific application. In the medical market, connectors are unique to their specific application and one solution does not work across the board.

Regulation is clear that, whenever possible, products intended to be sterile should be terminally sterilized in their final container. Only if terminal sterilization is not possible, filtration or aseptic assembly should be applied. This webinar will focus on elements to evaluate prior to selecting aseptic assembly for the manufacturing of sterile drug products.

Patient Support Programs (PSPs) have changed dramatically over the past decade; they have become global activities, and grown significantly in scale and complexity. While PSPs are also an increasingly valuable resource for pharmacovigilance due to the extensive patient safety data they generate, they have suffered from the traditional lack of standardized mechanisms for recording, reconciling and managing this data, resulting in resource heavy processes, and a lost opportunity for deeper product understanding for Pharma. Fortunately, new technologies are helping to tackle this challenge.

Various ways to implement continuous manufacturing in pharmaceutical development and production