Bio/Pharmaceutical Methods: Do your Analytical Methods Hold Up to Regulatory Scrutiny?
Eurofins BioPharma Product Testing
As FDA guidelines evolve and drug products on the market begin to age, bio/pharmaceutical manufacturers face scrutiny of the original methods used to support these products. Therefore, manufacturers must re-evaluate these methods to ensure they comply with current FDA expectations. Some manufacturers are even facing consent decrees imposed by the agency requiring them to bring methods up to current standards within a specified timeframe. This exercise requires significant amounts of time and resources, which many manufacturers do not have since they are focused on getting their next products to market. For that reason, some clients have been turning to Eurofins Lancaster Laboratories for support. More info >>
Following on from the success of the 2017 Outsourcing in
Clinical Trials Nordics conference, Arena International is pleased to announce
that the event will return for its 6th year in 2018.
The 2018 event welcomes biopharmaceutical and medical device
companies from across the Nordic region to share knowledge and challenges of
outsourcing and clinical operations. More info >>