Content provided by PRA Health Sciences | 09-Jul-2020
| White Paper
70% of medicines given to children have never been studied in pediatric populations. Children who need treatments represent a relatively small population....
Content provided by PRA Health Sciences | 09-Jul-2020
| White Paper
The pharmaceutical industry is unlike any other industry in that the products manufactured can dramatically improve, and even save, lives. This is especially...
Single-pass tangential flow filtration (SPTFF) is a method of ultrafiltration for the purposes of either volume reduction or protein concentration. This...
Content provided by BioContinuum™ Platform - MilliporeSigma | 01-Jul-2020
| Case Study
Perfusion involves the constant feeding of fresh media and removal of spent media and product while retaining high numbers of viable cells within the bioreactor...
Content provided by BioContinuum™ Platform - MilliporeSigma | 01-Jul-2020
| White Paper
Adoption of next generation processing and technologies can enable improvements in productivity by streamlining workflows, reducing the manufacturing plant...
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 | 01-Jun-2020
| Data Sheet
We are an established leader in flow cytometry services for clinical trials. Our technologies and solutions meet the growing global demand for enhanced...
Content provided by Q² Solutions | 01-May-2020
| Data Sheet
When a clinical trial requires local or point-of-care laboratory testing, managing the resulting data can be a significant burden to both the sponsor and...
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
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 | 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 Zymewire | 15-Aug-2019
| White Paper
The free Big Pharma R&D Spend report examines the financial performance and research & development investments of the top 25 pharmaceutical companies...
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 Catalent | 07-Nov-2018
| Case Study
A sponsor running a clinical trial in Israel arranged to ship their clinical trial product from Europe to a depot in Israel. With the protocol based in...
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 Marken | 26-Jun-2018
| Case Study
A desperate mother in Germany urged her team of doctors to reach out to a Marken client on behalf of her two year old girl. The child was battling leukemia...
Content provided by Baxter BioPharma Solutions | 12-Mar-2018
| White Paper
There are few challenges when increasing the scale of production for a solution formulation, but the challenges drastically increase when the formulation...
Content provided by Catalent | 05-Mar-2018
| White Paper
When planning a clinical trial, overlooking the importance of primary packaging can be a mistake. From stability concerns to labeling to patient compliance...
Baxter approaches formulation and process development with the intention of identifying the failure points for the product. Knowing where the product fails...
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...
Content provided by Eppendorf Bioprocess Solutions | 27-Jun-2017
| Infographic
DNA concentration, mastermix preparation, temperature management: Doing PCR like a pro can be more complex than it seems.The Eppendorf infographic helps...
Content provided by RSSL | 22-Mar-2017
| 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 Catalent | 23-Jan-2017
| White Paper
Clinical trials are more complex than ever before, driving the industry to develop and adopt new ways to manage clinical supplies and address new challenges.Fast...
Content provided by RSSL | 02-Nov-2016
| White Paper
Regulatory control of elemental impurities in pharmaceutical products has long been discussed, with both the European Pharmacopeia (EP) and the United...
Content provided by Butterworth | 13-Sep-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 SGS Life Science Services | 25-Apr-2016
| White Paper
Because of its use in the pharmaceutical and food industries, the USP has established standards relating to the amount of methoxyl and 2-hydroxypropoxyl...
Content provided by Oracle Health Sciences | 23-Mar-2016
| Case Study
Risk-based monitoring is coming into its own as an effective and pragmatic methodology to enhance patient safety while delivering significant efficiency...
Content provided by SANOFI - CEPiA | 09-Nov-2015
| White Paper
From a unique state-of-the-art platform for development and scale-up of Peptides and Oligonucleotides in Frankfurt (Germany), CEPiA offers customized services...
Content provided by Oracle Health Sciences | 01-Nov-2015
| White Paper
The new white paper, “Accelerating Data Cleaning, Integration & Analysis from Source to Submission,” examines how Oracle Health Sciences Data Management...
Content provided by Oracle Health Sciences | 22-Oct-2015
| Case Study
PPD, one of the top CROS worldwide, is reducing trial timelines, cost, and risk through simplified data exchange and monitoring with Oracle Siebel CTMS...
Content provided by World Courier | 12-Oct-2015
| Case Study
Two of the biggest challenges in today’s global clinical trials are patient recruitment and retention. These problems often spring from clinical trial...
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 Catalent | 31-Aug-2015
| White Paper
Viral clearance studies are mandated prior to entering clinical trials and for commercial launch of biopharmaceuticals. These studies are a key component...
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 World Courier | 16-Jun-2015
| Infographic
Download World Courier’s latest piece which shares the story of the changes in temperature-controlled transport and what these trends mean to your business....
Content provided by AdvantaPure® | 08-Jun-2015
| White Paper
Pharmaceutical fluid transfer involves many tubing-to-fitting connections, and unfortunately those connections can leak and result in contamination, production...
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 SGS Life Science Services | 20-Apr-2015
| White Paper
Within the pharmaceutical industry, there are six dominant methods used to model outsourcing strategy. This white paper details how a hybrid strategy can...
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...
Content provided by Catalent | 26-Jan-2015
| White Paper
Assessment of biosimilar molecules requires an orthogonal analytical approach. Any one particular analytical technique is not able to fully define the...
