Streamline your adoptive cell therapy program with digital PCR. Our team has a unique expertise in digital and quantitative PCR to support you in ensuring...
At CellCarta, we’re dedicated to working with our partners to further the limitless potential of precision medicine. Our broad technology offering is designed...
The manufacture of a drug product for clinical trials is of critical importance. The formulation, manufacturing, and assessment of a drug candidate during...
PerkinElmer | 15-Jul-2021
| Technical / White Paper
At Novartis, TIBCO Spotfire® enterprise analytics is a key tool for interactive graphical data analysis for preclinical and clinical studies. Using interactive...
Precision for Medicine | 01-Feb-2021
| Insight Guide
Immune monitoring has become an essential strategy for understanding, predicting, and monitoring the response of the immune system to therapeutic interventions....
Oracle Health Sciences | 14-Dec-2020
| Technical / White Paper
In just a few decades, clinical trials have changed dramatically. Twenty years ago, most of the data used in clinical research was entered on paper, but...
Cell therapy involves the transfer of genetically altered cells into a patient. As a global central laboratory services organization, we provide testing...
Telstar Life Science Solutions | 29-Jun-2020
| Case Study
Telstar case study. What is the impact of leading-edge innovative developments on the process analytical technology field for pharmaceutical systems and...
As a leading laboratory services organization for trials across the globe, we are proud to partner with clients to support COVID-19 clinical trials. Our...
We are an innovative, progressive and responsive partner with the global experience, medical expertise and focus on quality that is integral to drug, medical...
Baxter BioPharma Solutions | 01-Mar-2020
| Technical / White Paper
Recent market reports suggest increasing product niches, which may lead to decreasing numbers of units per product, making dedicated facilities less practical....
Frontage Laboratories | 01-Dec-2019
| Technical / White Paper
Biologics are complex large molecules derived from living organisms or manufactured from cells, and they have inherent structural heterogeneity. Indeed,...
Frontage Laboratories | 01-Oct-2019
| Technical / White Paper
Over the years, the pharmaceutical industry has made steady progress in improving the safety of drugs in development. Consequently, in 2015, only 14 percent...
Frontage Laboratories | 01-Oct-2019
| Technical / White Paper
Frontage is the first and only laboratory to validate Quanterix’ Simoa HD1 Analyzer for performing immunoassays. Most of the advanced instruments used...
Frontage Laboratories | 21-Aug-2019
| Technical / White Paper
Immunogenicity is the leading reason that biologics fail in clinical trials, and thus it has become imperative for drug development programs to include...
BBK Worldwide | 24-Jul-2019
| Technical / White Paper
Despite growing evidence, the myth that physicians won’t refer patients to clinical trials persists, perpetuated by the belief that they fear losing their...
Frontage Laboratories | 19-Jun-2019
| Technical / White Paper
Stability testing is, in essence, a quality control process and is there¬fore a vital component of every phase of clinical development for both large and...
In May 2018 Outsourcing-Pharma.com, in association with InnovoCommerce, conducted its second annual ‘state of the industry’ survey on its user base of...
Multiple myeloma is the second most common blood cancer in the world and despite survival rates increasing over the last decade, there remains a requirement...
In May 2017, Outsourcing-Pharma.com conducted its inaugural “state of the industry” survey of its user base of pharmaceutical industry professionals, including...
You have the power to make a difference. To make new therapeutics that improve quality of life and inspire a healthier world. To do this, you need a manufacturing...
The data used to determine the success of a cleaning validation is built upon both the effective evaluation of the manufacturing plant and the robustness...
Butterworth | 26-May-2016
| Technical / White Paper
The International Conference of Harmonisation (ICH) guidance document on elemental impurities, Q3D, reached step 4 in December 2014, meaning the final...
Oracle Health Sciences | 20-Apr-2016
| Technical / White Paper
The FDA has recommended the use of data mining to the drug industry, and their new Data Mining at FDA white paper summarizes their past and current data...
It’s time to look back and see how our predictions for this year fared, and take another look at the things we have written about since then.We examine...
The role of the Qualified Person (QP) in the pharmaceutical industry is mandated by law. Every holder of a relevant Manufacturers Authorisation (human...
Butterworth | 24-Sep-2015
| Technical / White Paper
The classic Modified Atmosphere Packaging (MAP) application, in the pharmaceutical industry, uses medical grade nitrogen to purge atmospheric oxygen and...
Billions of patients worldwide benefit from a diverse range of medical devices. The global medical device market in 2011 was approximately $300 billion...
Trimming your study budget is a good thing, right? When you can cut costs without compromising data integrity or accuracy, that's usually a positive....
ACM Global Central Laboratory | 19-May-2015
| Clinical Study
Until recently, sponsors and CROs engaged their central laboratory simply for routine safety testing. However, as clinical trial protocols have grown in...
Butterworth | 12-May-2015
| Technical / White Paper
Samplestorage, handling anddelivery are as important in the determination of residual solvents as the analysis itself. This paper provides practical advice...
Merge eClinical | 01-Apr-2015
| Technical / White Paper
Intense competition in the prescription drug market is driving pharmaceutical companies to expedite their drug discovery and development processes. Pharmaceutical...
Merck KGaA, Darmstadt, Germany | Recorded the 09-Apr-2015 | Webinar
Pyrogens in pharmaceuticals, medical devices, biotherapeutics and cosmetics can cause fevers in humans and are potentially life-threatening. Yet standard...
Butterworth | 27-Jan-2015
| Technical / White Paper
The European Pharmacopeia (Ph Eur) is moving away from the historical thin layer chromatography technique for the determination of Ninhydrin-positive substances,...
Reading Scientific Services Limited | 23-Oct-2014
| Technical / White Paper
Monoclonal antibodies are one of the most common types of biopharmaceuticals. Knowledge of an antibody’s molecular weight is essential; if this differs...
Maintaining the strict temperature parameters required to ensure product stability is relatively straightforward in the plant or laboratory setting, where...
Reading Scientific Services Limited | 11-Sep-2014
| Technical / White Paper
The role of the Qualified Person (QP) in the pharmaceutical industry is mandated by law (Directive 2001/83/EC, Directive 2001/20/EC, UK SI 2012/1916, UK...
Almac Group | 04-Aug-2014
| Technical / White Paper
UNDERSTANDING THE CHALLENGES OF TEMPERATURE CONTROLLED INVESTIGATIONAL MEDICINAL PRODUCT DISTRIBUTION IN EMERGING MARKETSTemperature deviation within the...
Worldwide, the pharmaceuticals market is anticipated to grow from more than USD 782 billion in 2011 to approach a value of just over USD 971 billion by...
Monoclonal antibodies are an important class of biopharmaceuticals. They are expressed from living cells and therefore, are subject to complex biochemical...
ACM Global Central Laboratory | 17-Jun-2014
| Clinical Study
Metabolic syndrome, a serious condition impacting adults and children in all genders, races and ethnicities, can lead to fatal outcomes if not detected...
Fujifilm Diosynth Biotechnologies | Recorded the 28-May-2014 | Webinar
The development of large scale E. coli expression systems can be rate limiting in process development. Fujifilm's pAVEway™ system combines innovative...
Butterworth | 06-May-2014
| Technical / White Paper
A method to identify the presence of heavy metals in pharmaceuticals was introduced in the United States Pharmacopoeia more than 100 years ago. Today pharmaceutical...
Incorporating adaptive design methodologies into clinical trials can reduce costs while maintaining trial integrity. Learn how these design strategies...
Vetter Pharma International GmbH | 15-Apr-2014
| Technical / White Paper
Realizing the full potential of an injectable drug compound is no small task. In the months and years that lead from the discovery phase to the rigorous...
With proposed changes to elemental impurities requirements for pharmaceutical products currently being reviewed, spectroscopic techniques for metals analysis...
