QA/QC

Understanding the hidden value of quality

Content provided by Thermo Fisher Scientific – Production Chemicals and Services | 16-Jan-2023 | White Paper

The raw material supply is too vital to leave to chance, and quality-related supply chain activities are cornerstones to your success.

Ensure a Flexible Supply Chain in Times of Global Turmoil

Content provided by Ancillare | 17-Aug-2022 | Insight Guide

As major world events continue to unfold, every organization is contending with supply chain disruptions.

How to resolve sticking issues in tablet production

Content provided by I Holland Limited - Tabletting Science | 24-Jun-2019 | Case Study

Tablet sticking is one of the most common problems in tablet manufacture. Find out how I Holland used the TSAR scientific predictive model and expert tablet...

How to measure powder and granule flow properties

Content provided by Stable Micro Systems | 01-Apr-2019 | White Paper

Being able to predict, optimise and control powder flow is of prime importance to manufacturers in ensuring high quality standards. Download this free...

Enabling drug traceability. Implementing serialization in practice as a CDMO.

R-Pharm Germany GmbH | Recorded the 10-Oct-2017 | Webinar

R-Pharm Germany has established an effective track & trace system to meet all regulatory requirements and to offer cost-effective and customer-oriented...

Cleaning Validation - What do you need to consider to ensure a successful outcome?

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...

pH measurement: Six technical tips

Content provided by Metrohm – customized analysis for the pharmaceutical industry | 10-Oct-2016 | White Paper

The pH value is one of the most important and therefore also one of the most frequently measured quantities in analytical chemistry. Sometimes a simple...

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

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...

FOR SALE/LEASE CRO/MRO turn key Research Campus, labs, vivariums, OR, archives, offices

Content provided by Northstar Private Capital LLC | 09-Aug-2016 | Product Brochure

Chazy, New York is located only six miles from the Canadian Border in Upstate New York. It is only ten minutes North of Plattsburgh, one hour south of...

Amino Acid Analysis of Pharmaceutical Products

Content provided by SGS Life Science Services | 11-Jul-2016 | White Paper

Amino Acid Analysis in general can be used for identification testing of biopharmaceutical active ingredients and the determination of impurities and related...

Considerations in Purchasing a LIMS

Content provided by Abbott Informatics | 27-Apr-2016 | White Paper

Many scientific enterprises find themselves in need of a Laboratory Information Management System (LIMS) to replace an incumbent system, whether an existing...

Advanced Analytics architecture and the benefits it serves as an integrated solution

Content provided by Abbott Informatics | 18-Apr-2016 | White Paper

A laboratory’s day-to-day operations are recorded through STARLIMS, accumulating data over time.This data includes sample lifecycle information and metadata.A...

Rapid Microbiological Method Statistics & Validation

EMD Millipore | Recorded the 17-May-2016 | Webinar

It is well known that implementation of Rapid Microbiological Methods in Pharma environments is accompanied by a large validation workload to ensure that...

Excellence in Pharmaceutical Analysis

Content provided by Butterworth | 01-Jan-2016 | Data Sheet

Butterworth specialise in Quality Control Analysis, Method Development, Validation & Stability Testing of Raw Materials, API, Finished Product and...

Live Webinar on Recent PAT applications for Softgels presented by Softigel by Procaps

Sofgen Pharmaceuticals | Recorded the 30-Nov-2015 | Webinar

Process Analytical Technologies (PAT) in solid dosages forms are commonly used for tablets. Procaps brings to you this webinar intended to present PAT...

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

Content provided by Butterworth | 23-Sep-2015 | White Paper

The classic Modified Atmosphere Packaging (MAP) application, in the pharmaceutical industry, uses medical grade nitrogen to purge atmospheric oxygen and...

Elemental Impurities for ICH Q3D, USP, and EP

Content provided by SGS Life Science Services | 15-Jun-2015 | White Paper

This white paper describes the risk assessment, implementation, and validation of the new elemental impurity guidelines. In order to meet the new standards...

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...

Amino Acid Analysis According to Ph.Eur 2.2.56

Content provided by SGS Life Science Services | 23-Feb-2015 | White Paper

Employing spectrophotometry and liquid chromatography quantitation of Ninhydrin-positive substances achieves 0.05% reporting sensitivity as required by...

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

Content provided by Butterworth | 03-Feb-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,...

Customized Biosimilarity Analytical Testing from Catalent

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...

OptiPact™ Technology Introduced by Catalent

Catalent Pharma Solutions, the leading global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health...

Using texture analysis in regenerative medicine

Research in the field of regenerative medicine is progressing at a rapid pace. Download this free white paper to find out how texture analysis can help...

Residual moisture in lyophilized pharmaceuticals

Content provided by Metrohm – customized analysis for the pharmaceutical industry | 15-Sep-2014 | Application Note

This method describes near-infrared spectroscopy in diffuse reflection for determining residual moisture in a lyophilized pharmaceutical product. The results...

Nondestructive, single tablet analysis

Content provided by Metrohm – customized analysis for the pharmaceutical industry | 16-Jun-2014 | Application Note

NIRS Spectroscopy allows rapid (<30 s) and nondestructive screening of solid dosage forms. It requires neither sample preparation nor solvent use. Interferences...

Determination of moisture in a protein sample using a portable NIR instrument

Content provided by Thermo Fisher Scientific | 03-Jun-2014 | Application Note

Near infrared spectroscopy has been used effectively to measure moisture in a wide variety of samples. Due to the large overtone band for water in NIR,...

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...

Near-infrared spectroscopy

Content provided by Metrohm – customized analysis for the pharmaceutical industry | 01-May-2014 | Application Note

NIRSystems Technology:  Improved productivity and faster quality control of starting materials, intermediates and final products. Learn more

Validation, Qualification and Calibration

Content provided by SGS Life Science Services | 21-Apr-2014 | White Paper

This white paper outlines outsourcing requirements for Validation, Qualification and Calibration activities in a pharmaceutical facility. These ongoing...

Want to Strengthen Your Supply Chain Security?

Content provided by Information not available | 18-Mar-2014 | Event Programme

The challenges of ensuring safe drugs for patients are universal, international and pervasive. The Global Forum on Access to Safe Medicines brings together...

Enhancing Actives Delivery for Optimal Formulation Efficacy

Content provided by Croda Inc | 24-Feb-2014 | Data Sheet

Excipients designed to enhance skin penetration can maximize the efficacy of topical formulations.  Through lipid disruption and skin polarity modification,...

Texture analysis for pharma QC

Looking for objective, reliable and cost-effective QC solutions? Download this free white paper to find out how texture analysis can help uphold quality...

NEOBEE® MCTs Enhance Pharmaceutical Bioavailability

Content provided by Stepan Lipid Nutrition | 04-Nov-2013 | White Paper

An efficient solvent for many lipophylic drugs and vitamins, NEOBEE® MCTs emulsify in aqueous environments and help uptake in intestinal cells. They are...

METHOD VALIDATION – USP PROPOSED <233>

Content provided by SGS Life Science Services | 04-Nov-2013 | White Paper

The USP is continuing to modify a proposal for using inductively coupled plasma (ICP) and ICP-mass spectroscopy (ICP-MS) to detect contaminating heavy...

Clinical Document distribution - Secure and Automated

Content provided by pharmasol | 04-Nov-2013 | Case Study

psiXchange automates the distribution of your safety related documents. The distribution engine handles country specific rules and user specific escalation...

CONFIDENCE IN BIOLOGICS FORMULATION DESIGN

Content provided by SGS Life Science Services | 07-Oct-2013 | White Paper

To ensure a long product shelf-life for biopharmaceutical drug products, a stable storage environment is critical. Determination of the optimal environment...

Analysis of Biopharmaceuticals to Conform to ICHQ6B

Content provided by RSSL | 25-Sep-2013 | 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...

Cell Culture Media Identification with Handheld 1064 Nanometer Raman

Content provided by Rigaku Raman Technologies | 23-Sep-2013 | Application Note

Biopharmaceutical production is a rapidly growing and high risk industry. According to a market research report, only three of ten drugs receive market...

Pharmaceutical Material Identification

Content provided by Thermo Fisher Scientific | 18-Sep-2013

Thermo Scientific TruScan RM and microPHAZIR RX analyzers are revolutionary instruments that can help you achieve compliance and realize a rapid return...

Handheld 1064nm Raman boosts excipient analysis capacity

Content provided by Rigaku Raman Technologies | 21-Aug-2013 | Application Note

Pharmaceutical manufacturers the world over seek more efficient technologies for materials validation. Implementation of handheld Raman spectrometers utilising...

Exploring New Frontiers in Direct to Patient Home Delivery Services for Clinical Trials Materials

Marken | Recorded the 10-Sep-2013 | Webinar

Exploring New Frontiers in Direct to Patient (DTP) Home Delivery Services for Clinical Trial Materials provides an in-depth look at reasons to consider...

Avoid Angry Customers-Eliminate Defects

Content provided by METTLER TOLEDO | 12-Jun-2013 | White Paper

In the pharmaceutical business, it is crucial that containers be free of contamination, formation defects and dimensional irregularities to avoid the risk...

Id Counterfeit Pharmaceuticals with Portable Raman

Content provided by Rigaku Raman Technologies | 22-May-2013 | White Paper

The growing danger of counterfeit and substandard medicines entering the supply chain is a concern for global pharmaceutical manufacturers and consumers....

Increase Integrity of Single-use Assemblies Immediately Before Use.

Content provided by ATMI Life Science | 20-May-2013 | White Paper

Discover the HIT™ platform, a new highly-sensitive technology for detecting defects as small as 10 micron in single-use assemblies at the end-user facility.Learn...

Extractables & Leachables Risk Assessment

Content provided by SGS Life Science Services | 04-Feb-2013 | White Paper

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

Assessing pharma gels

Want to create succesful pharmaceutical gels? Discover how objective texture analysis can accelerate NPD, ensure consistent quality and maximise consumer...

Analytical Method Development and Validation — A CDMO Perspective

Content provided by DPT Laboratories | 05-Dec-2012 | Insight Guide

Pharmaceutical drug product development can be an expensive and time consuming process. Many challenges are faced by pharmaceutical development companies...

Metrohm

Content provided by Metrohm – customized analysis for the pharmaceutical industry | 15-Oct-2012 | Application Note

The determination of low-molecular-weight aliphatic amines in interfering matrices is a challenging task because the protonated amines are often poorly...

Material Identification Made Simple

Content provided by Thermo Fisher Scientific | 01-Oct-2012

Together, TruScan RM and microPHAZIR RX let you identify 90% of pharmaceutical compounds in seconds.  With both instruments you’ll quickly and effectively...

Radio Ion Chromatography

Content provided by Metrohm – customized analysis for the pharmaceutical industry | 17-Sep-2012 | Data Sheet

Radio Ion ChromatographyPositron emission tomography (PET) is one of the most powerful noninvasive diagnostic tools for tracing organ functioning. Quality...