APIs (active pharmaceutical ingredients)

69 Results

Eastern & Western Manufacturing Solutions

Eastern & Western Manufacturing Solutions

Piramal Pharma Solutions | 15-Mar-2022 | Technical / White Paper

The best manufacturing site for a product can change throughout the life cycle. When bringing new drugs to market, biopharma companies may benefit from...

Flexibility and capability in pre-filled syringes

Flexibility and capability in pre-filled syringes

Curia | 15-Nov-2021 | Technical / White Paper

Pre-filled syringes have risen in popularity in recent years but the pandemic’s impact on drug development, manufacturing and patient care has created...

LACTIUM®: dairy bioactive to soothe your pet

LACTIUM®: dairy bioactive to soothe your pet

Ingredia | 12-Oct-2021 | Infographic

Lactium® gives you the chance to better meet your pet’s needs for a more harmonious life together. Lactium® acts on the brain and has no side-effects,...

Facilities: Lexington, KY USA

Facilities: Lexington, KY USA

Piramal Pharma Solutions | 23-Aug-2021 | Insight Guide

The Piramal Pharma Solutions facility in Lexington, KY USA is a fully integrated site which offers analytical, formulation development, and manufacturing...

Facilities: Sellersville, PA USA

Facilities: Sellersville, PA USA

Piramal Pharma Solutions | 23-Aug-2021 | Insight Guide

The Piramal Pharma Solutions facility in Sellersville, PA USA is a fully integrated site that offers product and process development, clinical supply and...

Facilities: Morpeth, UK

Facilities: Morpeth, UK

Piramal Pharma Solutions | 26-Jul-2021 | Insight Guide

The Piramal Pharma Solutions facility in Morpeth, UK offers Active Pharmaceutical Ingredients (APIs) and oral solid drug product development, clinical...

Facilities: Riverview, MI USA

Facilities: Riverview, MI USA

Piramal Pharma Solutions | 26-Jul-2021 | Insight Guide

The Piramal Pharma Solutions facility in Riverview, MI, USA can support your Drug Substance (API) needs. The site has extensive experience in safely delivering...

Integrated Solutions for Accelerated Time to Market

Integrated Solutions for Accelerated Time to Market

Piramal Pharma Solutions | 08-Jun-2021 | Technical / White Paper

Facing capacity constraints? Lock in your program now! With 14 sites around the world providing diverse services ranging from discovery to drug substance...

Lactium, your ally to manage day to day stress

Lactium, your ally to manage day to day stress

Ingredia | 27-Aug-2020 | Product Presentation

Stress has been called the ‘health epidemic of the 21st century’ by the World Health Organization. Increasingly, consumers are looking for safe, reliable...

Strategies to Select and Deliver the Right Candidate

Strategies to Select and Deliver the Right Candidate

Catalent Pharma Solutions | 05-Mar-2018 | Technical / White Paper

Does your candidate have what it takes to succeed? Do you have the information needed to make the right decisions about your candidate’s path to the clinic?...

Why managing variability?

Why managing variability?

SIO/ADM | 02-Oct-2017 | Research Study

Significant efforts are necessary to develop an active pharmaceutical ingredient (API). It is therefore risky to expose this API to poorly characterized...

VALSYNTHESE – Custom phosgenation under GMP

VALSYNTHESE – Custom phosgenation under GMP

Valsynthese SA | 01-Mar-2017 | Technical / White Paper

Phosgene is a powerful reagent allowing the straightforward synthesis of key intermediates such as chloroformates, acid chlorides, and carbamoyl chlorides....

Producing the perfect soft gel

Producing the perfect soft gel

Leading manufacturer of gelatine and collagen peptides | 17-Jan-2017 | Technical / White Paper

This white paper outlines the key considerations to ensure gelatin is enhanced for soft gel formulation, efficient gel production and optimal API delivery...

Patient-Centric Drug-Development Process

Patient-Centric Drug-Development Process

Catalent Pharma Solutions | 28-Nov-2016 | Insight Guide

For large and small pharmaceutical companies alike; developing a new drug is fraught with risk. Patient-centric drug development and optimization is both...

pH measurement: Six technical tips

pH measurement: Six technical tips

Metrohm – customized analysis for the pharmaceutical industry | 10-Oct-2016 | Technical / 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...

Abbott_Whitepaper-Considerations-in-purchasing-a-LIMS_Web

Considerations in Purchasing a LIMS

Abbott Informatics | 27-Apr-2016 | Technical / White Paper

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

High energetic and Phosgene reactions in safe hands

High energetic and Phosgene reactions in safe hands

Valsynthese SA | 01-Mar-2016 | Technical / White Paper

Valsynthese, expert in high energetic and hazardous fine chemical production of key intermediates and APIs, is devoted to delivering high quality services...

Probiota 2016 Conference Programme

Probiota 2016 Conference Programme

Probiota | 05-Jan-2016 | Event Programme

NutraIngredients’ Probiota is the leading annual event for the global prebiotic, probiotic and the microbiota focused food and pharma industries and in...

Excellence in Pharmaceutical Analysis

Excellence in Pharmaceutical Analysis

Butterworth | 01-Jan-2016 | Data Sheet

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

Amino Acid Analysis According to Ph.Eur 2.2.56

Amino Acid Analysis According to Ph.Eur 2.2.56

SGS Life Science Services | 23-Feb-2015 | Technical / White Paper

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

USP<233> Elemental Impurities Sample Prep Strategy

USP<233> Elemental Impurities Sample Prep Strategy

SGS Life Science Services | 03-Nov-2014 | Technical / White Paper

Although USP <232> and <233> are still under discussion, a good deal of work is going on ahead of implementation in terms of method development....

Optimizing API Stability Through Purity

Optimizing API Stability Through Purity

Croda Inc | 21-Jul-2014

It is crucial to optimize your drug active’s environment to ensure the stability of the API.  A high purity excipient can help by minimizing the occurrence...

Steris

Do you have spores?

Steris: A global leader in infection prevention and contamination control | 27-May-2014 | Technical / White Paper

Trending analysis of cleanroom environmental monitoring data sometimes shows the presence of spores. These undesirable microbes must be eradicated quickly...

JRS Pharma LP

Excipients for Multilayer Tablets

JRS PHARMA | 07-May-2014 | Technical / White Paper

Multi-layered tablets bring together differently formulated powder mixtures, which typically contain different APIs, into a single tablet with two or more...

Butterworth

Elemental Impurity Analysis in Pharmaceuticals

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...

Near-infrared spectroscopy

Near-infrared spectroscopy

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

Want to Strengthen Your Supply Chain Security?

Want to Strengthen Your Supply Chain Security?

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...

SGS Group Management

Method Validation for Heavy Metals Testing

SGS Life Science Services | 04-Mar-2014 | Technical / White Paper

USP proposed <232> and <233> changes require ICP and ICP-MS instrumentation and methodology expertise, and knowledge of sample preparation....

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