Bulk ingredients

HEALTH IS A JOINT PROJECT INDENA’S NEXT-GENERATION CDMO

Content provided by Indena | 15-Mar-2023 | White Paper

Indena’s Custom Development & Manufacturing Organization services offer a full range of manufacturing capabilities for pharmaceutical ingredients including...

Outsourcing Analytical Testing for Biologics - A CRO's Perspective

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,...

How to Avoid Surprises in Small-Molecule Drug Development Programs

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...

Validating The Simoa Technology

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...

Assessing Pre-Existing Antibodies in Biotheraputic Development

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...

The Truth about Physician Referrals and Clinical Trials

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...

Survey Report: State of the global pharmaceutical contract services industry 2018

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...

The Power to Make, A Virtual Tour

Content provided by Althea | 24-Mar-2017

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...

Elemental Impurity Analysis in Pharmaceuticals – The Road To Implementation of ICH Q3D

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...

Enhanced Sampling and Calibration Procedures for the Analysis of Residual Oxygen in Nitrogen Purged Pharmaceutical Packaging by GC-TCD

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...

Enhanced Residual Solvents Analysis: A Practical Approach to Sampling, Delivery, Storage and Analysis.

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...

The whole blood assay: Detection of broad spectrum of pyrogens & examples of medical device testing

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...

A Method to Meet the New Ph Eur Ninhydrin-Positive Substances Requirement

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,...

Learn the risk factors of metabolic syndrome and the role central labs play in aiding its detection

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...

Elemental Impurity Analysis in Pharmaceuticals

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...

Controlled Release and Bioavailability Enhancement

Content provided by Information not available | 28-Oct-2013 | Case Study

Metrics provides product development that leverages proprietary pharmaceutical technologies in the areas of: • Customized Controlled Release Drug Delivery...

Biosimilars – Landmark Developments Point to the Future for Regulations and Analysis

SGS Life Science Services | Recorded the 09-Oct-2013 | Webinar

2013 is a landmark year for biosimilars, with the approval of the first biosimilar mAb and regulatory developments across the globe. Correctly interpreting...

Best Practices for Achieving and Maintaining Aseptic Conditions During Sterility Testing

Content provided by SGS Life Science Services | 03-Dec-2012 | White Paper

Sterility testing is required for companies producing pharmaceutical products and consistent and meticulous testing is essential to obtain results that...

INFLUENZA TREATMENT CLINICAL TRIALS: CLINICAL CASE STUDIES

Content provided by SGS Life Science Services | 19-Nov-2012 | White Paper

Development of influenza vaccines is critical; but, there is also a need for new influenza treatments. This article presents an overview of challenges...

Extractables & Leachables Risk Assessment

Content provided by SGS Life Science Services | 22-Oct-2012 | Case Study

An extractables and leachables case study describes how a comprehensive risk assessment was performed across the entire production process of a European...

New Early Phase Concepts: Practical Implementation

Content provided by SGS Life Science Services | 03-Sep-2012 | White Paper

There is an urgent need to use innovative techniques in early development. This paper will discuss several case studies in which new clinical trial methods...

Vaccine-Based Clinical Trials

Content provided by SGS Life Science Services | 09-Jul-2012 | White Paper

Download this paper to read two case studies which illustrate strategies for planning and implementing a vaccine-based infectious disease clinical trial...

Sample Prep Proposed USP<233> Elemental Impurities

Content provided by SGS Life Science Services | 27-Feb-2012 | White Paper

Proper sample preparation is crucial when analyzing for trace metals using inductively coupled plasma (ICP). This paper illustrates how solubility of the...

New Challenges in Early Clinical Development

Content provided by SGS Life Science Services | 24-Jan-2012 | White Paper

With many new challenges in early clinical development there is pressure to change how early phase clinical trials are conducted where the final goal is...

Improving Signal Detection in Drug Safety

Content provided by SGS Life Science Services | 07-Nov-2011 | White Paper

Early identification and management of emerging drug safety issues are a major concern of industry stakeholders. Electronic capture systems for AE reporting...

White Paper: Vaccine-Based Clinical Trials

Content provided by SGS Life Science Services | 26-Sep-2011 | White Paper

Download this paper to read two case studies which illustrate strategies for planning and implanting a vaccine-based infectious disease clinical trial...

Generate Sales Leads: Free White Paper

Content provided by William Reed | 02-Aug-2010 | White Paper

White papers (or technical papers) are one of the most effective ways to generate leads for your sales team and establish your company’s reputation as...

Generate sales leads with a good white paper

Content provided by William Reed | 24-Mar-2010 | White Paper

White papers (or technical papers) are one of the most effective ways to generate leads for your sales team and improve your company’s reputation as an...

Micro Reactors - The Future for Cost-Effective Manufacturing

DSM PHARMACEUTICAL PRODUCTS | Recorded the 26-Aug-2009 | Webinar

Leading scientists from DSM speak about micro reactor technology for the sustainable production of API’s to “go green” while introducing cost-effective...

Publish your Technical Paper on this Website

Content provided by William Reed | 09-Jun-2009

Promote your company’s technical expertise towards decision makersPublish your Technical Paper on this website.Benefits:· 71% of industry professionals...

Harmonized Pharmaceutical Microbiology: SGS Technical Bulletin

Content provided by SGS Life Science Services | 01-Jul-2008 | White Paper

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Bulk ingredients

31 Results

HEALTH IS A JOINT PROJECT INDENA’S NEXT-GENERATION CDMO

Outsourcing Analytical Testing for Biologics - A CRO's Perspective

How to Avoid Surprises in Small-Molecule Drug Development Programs

Validating The Simoa Technology

Assessing Pre-Existing Antibodies in Biotheraputic Development

The Truth about Physician Referrals and Clinical Trials

Survey Report: State of the global pharmaceutical contract services industry 2018

The Power to Make, A Virtual Tour

Elemental Impurity Analysis in Pharmaceuticals – The Road To Implementation of ICH Q3D

Enhanced Sampling and Calibration Procedures for the Analysis of Residual Oxygen in Nitrogen Purged Pharmaceutical Packaging by GC-TCD

Enhanced Residual Solvents Analysis: A Practical Approach to Sampling, Delivery, Storage and Analysis.

The whole blood assay: Detection of broad spectrum of pyrogens & examples of medical device testing

A Method to Meet the New Ph Eur Ninhydrin-Positive Substances Requirement

Learn the risk factors of metabolic syndrome and the role central labs play in aiding its detection

Elemental Impurity Analysis in Pharmaceuticals

Controlled Release and Bioavailability Enhancement

Biosimilars – Landmark Developments Point to the Future for Regulations and Analysis

Best Practices for Achieving and Maintaining Aseptic Conditions During Sterility Testing

INFLUENZA TREATMENT CLINICAL TRIALS: CLINICAL CASE STUDIES

Extractables & Leachables Risk Assessment

New Early Phase Concepts: Practical Implementation

Vaccine-Based Clinical Trials

Sample Prep Proposed USP<233> Elemental Impurities

New Challenges in Early Clinical Development

Improving Signal Detection in Drug Safety

White Paper: Vaccine-Based Clinical Trials

Generate Sales Leads: Free White Paper

Generate sales leads with a good white paper

Micro Reactors - The Future for Cost-Effective Manufacturing

Publish your Technical Paper on this Website

Harmonized Pharmaceutical Microbiology: SGS Technical Bulletin

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