Content provided by CellCarta | 08-Aug-2022
| Case Study
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...
Content provided by CellCarta | 17-Jan-2022
| Product Presentation
At CellCarta, we’re dedicated to working with our partners to further the limitless potential of precision medicine. Our broad technology offering is designed...
Content provided by Altasciences | 13-Dec-2021
| Case Study
The manufacture of a drug product for clinical trials is of critical importance. The formulation, manufacturing, and assessment of a drug candidate during...
Content provided by PerkinElmer | 15-Jul-2021
| White Paper
At Novartis, TIBCO Spotfire® enterprise analytics is a key tool for interactive graphical data analysis for preclinical and clinical studies. Using interactive...
Content provided by 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....
Content provided by Oracle Health Sciences | 14-Dec-2020
| 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...
Content provided by Q² Solutions | 01-Sep-2020
| Clinical Study
Cell therapy involves the transfer of genetically altered cells into a patient. As a global central laboratory services organization, we provide testing...
Content provided by 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...
Content provided by Q² Solutions | 10-Jun-2020
| Clinical Study
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...
Content provided by Q² Solutions | 17-Apr-2020
| Product Brochure
We are an innovative, progressive and responsive partner with the global experience, medical expertise and focus on quality that is integral to drug, medical...
Content provided by Baxter BioPharma Solutions | 01-Mar-2020
| White Paper
Recent market reports suggest increasing product niches, which may lead to decreasing numbers of units per product, making dedicated facilities less practical....
Content provided by Frontage Laboratories | 01-Dec-2019
| White Paper
Biologics are complex large molecules derived from living organisms or manufactured from cells, and they have inherent structural heterogeneity. Indeed,...
Content provided by Frontage Laboratories | 01-Oct-2019
| White Paper
Frontage is the first and only laboratory to validate Quanterix’ Simoa HD1 Analyzer for performing immunoassays. Most of the advanced instruments used...
Content provided by Frontage Laboratories | 01-Oct-2019
| 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...
Content provided by Frontage Laboratories | 21-Aug-2019
| 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...
Content provided by BBK Worldwide | 24-Jul-2019
| 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...
Content provided by Frontage Laboratories | 19-Jun-2019
| 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...
Content provided by William Reed | 11-Jul-2018
| Research Study
In May 2018 Outsourcing-Pharma.com, in association with InnovoCommerce, conducted its second annual ‘state of the industry’ survey on its user base of...
Content provided by Recipharm AB | 04-Sep-2017
| Case Study
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...
Content provided by William Reed | 27-Jul-2017
| Application Note
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...
Content provided by RSSL | 14-Jun-2016
| White Paper
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...
Content provided by Butterworth | 26-May-2016
| White Paper
The International Conference of Harmonisation (ICH) guidance document on elemental impurities, Q3D, reached step 4 in December 2014, meaning the final...
Content provided by Oracle Health Sciences | 20-Apr-2016
| 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...
Content provided by World Courier | 07-Dec-2015
| Case Study
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...
Content provided by RSSL | 14-Oct-2015
| White Paper
The role of the Qualified Person (QP) in the pharmaceutical industry is mandated by law. Every holder of a relevant Manufacturers Authorisation (human...
Content provided by Butterworth | 24-Sep-2015
| White Paper
The classic Modified Atmosphere Packaging (MAP) application, in the pharmaceutical industry, uses medical grade nitrogen to purge atmospheric oxygen and...
Content provided by RSSL | 02-Jul-2015
| White Paper
Billions of patients worldwide benefit from a diverse range of medical devices. The global medical device market in 2011 was approximately $300 billion...
Content provided by Merge eClinical | 24-Jun-2015
| Clinical Study
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....
Content provided by 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...
Content provided by Butterworth | 12-May-2015
| White Paper
Samplestorage, handling anddelivery are as important in the determination of residual solvents as the analysis itself. This paper provides practical advice...
Content provided by Merge eClinical | 01-Apr-2015
| 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...
Content provided by Butterworth | 27-Jan-2015
| White Paper
The European Pharmacopeia (Ph Eur) is moving away from the historical thin layer chromatography technique for the determination of Ninhydrin-positive substances,...
Content provided by Reading Scientific Services Limited | 23-Oct-2014
| 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...
Content provided by World Courier | 20-Oct-2014
| Application Note
Maintaining the strict temperature parameters required to ensure product stability is relatively straightforward in the plant or laboratory setting, where...
Content provided by Reading Scientific Services Limited | 11-Sep-2014
| 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...
Content provided by Almac Group | 04-Aug-2014
| White Paper
UNDERSTANDING THE CHALLENGES OF TEMPERATURE CONTROLLED INVESTIGATIONAL MEDICINAL PRODUCT DISTRIBUTION IN EMERGING MARKETSTemperature deviation within the...
Content provided by RSSL | 24-Jul-2014
| White Paper
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...
Content provided by RSSL | 19-Jun-2014
| White Paper
Monoclonal antibodies are an important class of biopharmaceuticals. They are expressed from living cells and therefore, are subject to complex biochemical...
Content provided by 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...
Content provided by Butterworth | 06-May-2014
| 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...
Content provided by Vetter Pharma International GmbH | 15-Apr-2014
| 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...
Content provided by RSSL | 28-Nov-2013
| White Paper
With proposed changes to elemental impurities requirements for pharmaceutical products currently being reviewed, spectroscopic techniques for metals analysis...
