Pharma IQ Members

Manufacturing

Gain a solid foundation for your manufacturing process, mitigate risks and ensure compliance. Pharma IQ is proud to provide an international, non-biased, central resource, for professionals working in domestic and overseas manufacturing to exchange ideas on best practice and share case studies on innovation within the area.

Contributor: Miss Chanice Henry
Posted: 12/04/2016
Miss Chanice Henry
The first quarter of 2016 hosted plenty of activity from the pharma and cold chain industries. This was seen in the form of patent challenges, landmark agreements, extreme market reactions as well as a nationwide medicine ban for hundreds of products. Read on for this quarter’s highlights from Pharma IQ Full Article »
Contributor: Gerald Clarke
Posted: 12/03/2014
The pharma industry has a lot to learn from the food and beverage industry when it comes to contract manufacturing. To get to grips with this outsider's view, we spoke with Steve Hills, European Contract Manufacturing Director at Pepsico. Steve outlines where companies can go wrong in working with CMOs Full Podcast »
Contributor: Tony Hitchcock
Posted: 22/03/2016
Tony Hitchcock
When we look at the current trends with what we can refer to as “next generation therapeutics”, whether it be ADCs or cell and gene therapy products, one trend is very clear, products are becoming increasingly complex in their nature. Certainly, the complexity of the manufacturing processes used to produce them clearly reflects this; hand in hand with ever increasing product development costs and timelines. Full Column »
Contributor: Chanice Henry
Posted: 28/04/2016
Chanice Henry
While the US advances with its coverage of medical device classes within the U.S. Food and Drug Administration (FDA) Unique Device Identification regime, other countries around the globe are progressing their own track and trace strategies for medical devices. Through the collaboration of the world’s regulatory agencies it is hoped that a synchronized approach to medical device identification will be achieved on an international level, amidst their efforts to tackle counterfeiting, increase accountability and enable safety corrective measures. (2) Full Whitepaper »