APIs (active pharmaceutical ingredients)

70 Results

The Performance of PROSOLV® EASYtab SP in 4 Medium-Dose, Direct Compression Formulations

JRS PHARMA | 30-Sep-2022 | Technical / White Paper

In the present study, the performance of PROSOLV® EASYtab SP was tested in four DC formulations with different model APIs.

Pediatric Formulations: Identifying & Addressing Children’s Needs

Piramal Pharma Solutions | 30-Jun-2022 | Technical / White Paper

Developing formulations for pediatric patients poses unique challenges. The specific needs of children, which vary by age, mean the task goes beyond scaling...

Nanomilling for Better Solubility and Bioavailability

Altasciences | 07-Apr-2022 | Technical / White Paper

40% of marketed drugs and 90% of active pharmaceutical ingredients (APIs) are poorly water-soluble. Nanomilling is a proven technique that can overcome...

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

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...

INDENA’S CUSTOM DEVELOPMENT AND MANUFACTURING SERVICES FOR APIS AND HPAPIS

Indena | 08-Nov-2021 | Technical / White Paper

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

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,...

Overcoming Solubility Challenges with Liquid-Filled Capsules

Altasciences | 28-Sep-2021 | Technical / White Paper

Poorly soluble molecules comprise more than 70% of the small molecule products entering the drug development pipeline today, and are difficult to formulate...

Bioavailability Enhancement Techniques to Improve Patients' Lives

Piramal Pharma Solutions | 16-Sep-2021 | Technical / White Paper

Oral bioavailability is a constant challenge for developers of new chemical entities. Low solubility and permeability often reduce the fraction of an orally...

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

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...

Lactium® significantly reduces stress-related symptoms

Ingredia | 05-Aug-2021 | Product Brochure

Lactium® is a milk protein hydrolysate which contains a bioactive decapeptide with soothing properties called α-casozepine. It decreases anxiety-related...

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

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

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

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...

Accelerated development of first-in-human programs. Lonza’s SimpliFiH® Solutions

Lonza | 25-Aug-2020 | Sponsored Link

The presented program is laid out as integrated Drug Substance, Particle Engineering and Drug Product services, enabling drug substance and drug product...

INDENA'S INNOVATIVE TECHNOLOGY FOR THE APIS MARKET

Indena | 08-May-2019 | Application Note

A pilot pharmaceutical plant for small scale productions and a new spray drying system are the new suites Indena will open at its main production site,...

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?

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 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

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

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

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...

A unique pharmaceutical oil for solubility and oral bioavailability enhancement

Gattefossé | 01-Oct-2016 | Technical / White Paper

This white paper features Maisine® CC, Gattefossé’s tradename for glyceryl monolinoleate (USP-NF), also known as corn oil mono-, di- and triglycerides....

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

Butterworth | 13-Sep-2016 | Technical / White Paper

The International Conference of Harmonisation (ICH) guidance document on elemental impurities, Q3D, reached step 4 in December 2014, meaning the final...

Influence of AFFINISOL™ viscosity on HME processability and drug release

Information not available | 12-Sep-2016 | Technical / White Paper

Four grades of AFFINISOL™ HPMC HME were synthesized to specific target viscosities to first assess the ability to control the dissolution rate of a poorly...

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

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...

How to Successfully Combine Multiple APIs Into a Single Dose

JRS PHARMA | Recorded the 07-Jun-2016 | Webinar

Over the years, multiple active pharmaceutical ingredients (API) have been successfully combined into single dosage forms primarily through tablets and...

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...

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

Abbott Informatics | 18-Apr-2016 | Technical / 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...

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...

Next Generation HPMC Capsules: Bioequivalence and Functional Performance

Capsugel | Recorded the 17-Feb-2016 | Webinar

Two-piece hard shell capsules made from hydroxypropyl methylcellulose (HPMC) are emerging as an alternative to conventional gelatin capsules for oral drug...

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

Butterworth | 01-Jan-2016 | Data Sheet

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

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

Butterworth | 23-Sep-2015 | Technical / 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.

Butterworth | 12-May-2015 | Technical / 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

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...

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

Butterworth | 03-Feb-2015 | Technical / White Paper

The European Pharmacopeia (Ph Eur) is moving away from the historical thin layer chromatography technique for the determination of Ninhydrin-positive substances,...

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....

Comparison Trials on Herbal Extract Syrups Based on LYCASIN® 80/55 and Simple Sucrose

Roquette Pharma Solutions | 01-Sep-2014 | Case Study

Formulating a sugar-free syrup being at the same time stable and with a pleasant taste can be a real challenge. LYCASIN®, a liquid maltitol with a sweet...

Technology Selection To Enhance Oral Bioavailability

Capsugel | 20-Aug-2014 | Technical / White Paper

Effective technology selection for improving bioavailability (BA) can accelerate the development of promising compounds and reduce the overall cost and...

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...

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

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,...

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...

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...

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

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

CREMER OLEO has become the holder of the first CEP ever granted for a Medium-Chain Triglyceride (MIGLYOL® 812 N).

CREMER OLEO GmbH & Co. KG | 28-Apr-2014 | Press Release

CREMER OLEO has gathered its activities for the pharmaceutical industry under the roof of CREMER Health, with a strong commitment to quality leadership...

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...