eCTDmanager™ - Electronic and Paper Publishing All in One Solution

February-2010

eCTDmanager is an off-the-shelf scalable "all-in-one" electronic submission management solution for eCTD and non-eCTD electronic and paper submissions. eCTDmanager enables users to easily build, view, validate and publish (electronic and paper) compliant submissions based on CTD, eCTD, NeeS, IMPD, CTA and other submission structures. For more information, please download this free white paper.

EURS is Yours™ - The eCTD Specification

February-2010

EURS is Yours is a multifunctional software solution that serves as an overall eCTD validation and retrieval software tool. It reports whether a submitted eCTD-based application conforms to the official interpretation of the eCTD format. For more information, please download this free white paper.

Effect of the Combination of Alinidine and Other Anti-Anginal Drugs on Heart Rate and Blood Pressure in Healthy Volunteers

January-2010

Heart rate and blood pressure changes following the administration of alinidine 30mg alone and in combination with atenolol 25mg, nifedepine retard 20mg and glyceryl trinitrate 500μg were investigated in three groups of six healthy male volunteers.

Effect of MAO-A Inhibition on the Pharmacokinetics of Almotriptan, an Antimigraine Agent in Humans

January-2010

A study assessing the effect of a reversible MAO-A Inhibitor, moclobemide, on the singel-dose pharmacokinetices of almotriptan and assess the clinical consequences of any interaction.

Effect of Cimetidine and Rifampicin on the Metabolism of Alinidine

January-2010

Studies with alinidine have indicated some metabolism to clonidine, in both patietns and healthy volunteers. The present study investigated the effects of an enzyme inhibitor, cimetidine, and an enzyme inducer, rifampicin, on the metabolism of alinidine to clonidine.

eSubmissions: Past, Present and Future

December-2009

The pharmaceutical industry has realised for some time the value of eSubmissions. However, as we all know, the regulatory filings in the pharmaceutical industry are large, complex and sophisticated. The technology and procedures to meet these challenges have evolved significantly over the years. This article will review some of this evolution and highlight the current issues and trends for the filings of tomorrow.

Enabling Drug Delivery Deal Making

October-2009

Transdermal drug delivery: Time for a closer look. To find out more download this free white paper.

Enterprise-Level Change Control: A Life Science Business Imperative

September-2009

Free white paper: Change control in life science organisations is a critical business issue in terms of risk, safety and business performance - and it cannot be short-changed.

Engineering

September-2009

This free white paper includes information on NEPIC's role within North East England's engineering community.

Ensuring Patient Safety through Supply Chain Control and GMP

August-2009

The Parenteral Drug Association (PDA) is the leading global provider of science, technology and regulatory information and education for the pharmaceutical and biopharmaceutical community.

Emerging Markets: Clinical Trials, India (Krathish Bopanna)

July-2009

Based on our local up-to-date knowledge in the regions we are working in, we guide you through a smooth approval process for your trials.

Establishing the Standards in Biomarker Research

July-2009

Patent, pipeline and competitor knowledge to help you optimize your IP portfolio, monitor industry developments and make better decisions.

Evaluating the QT-Liability of a Drug During its Development

July-2009

E-WorkBook Suite v8.0

July-2009

Identify potential drug candidates faster and more accurately

Effective Photo Stability Testing

June-2009

EqualAudit

May-2009

Independent Verification Of Clinical Dose Calculations For Simple And Advanced Radiotherapy Techniques (3D-CRT, IMRT)

Equal Pharma Brochure

May-2009

Independent Verification Of Clinical Dose Calculations For Simple And Advanced Radiotherapy Techniques (3D-CRT, IMRT)