News and Research

Network System Architect (Part-time)

Jun 29, 2018

  Overview Clinical Trial Endpoint has an exciting opportunity for an experienced Network System Architect who is seeking to grow and diversify their career. We are a highly innovative company who developed a healthcare technology application – ‘RealWorld EDC’. This application was specifically designed for the collection of patient data in the real world setting…

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Patient-Centred Healthcare

Jun 21, 2018

Putting the patient at the centre of treatment is a long-appreciated goal in healthcare and it describes a model where decision-making is shared between multiple stakeholders. In the past, the needs of the physician used to be the main focus of pharmaceutical marketing, while today “the customer” comprehends: doctors, nurses, non-clinical staff, and of course…

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Postmarketing Surveillance Study, why is it important?

Jun 15, 2018

When manufacturing a new medical product, such as new drugs or therapies, pharmaceutical companies go through clinical trials to ensure that products are safe, effective and efficacious. Although these trials are heavily regulated processes, not all side effects of a drug – Adverse Drug Reactions (ADR) – can’t be anticipated. This is mainly because: Tests in…

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The importance of RealWorld Data to healthcare

May 3, 2018

Medical care and biomedical research have experienced a data revolution in the past years, and RealWorld Data is deeply connected to it. Clinical trials play a critical role in reviewing the safety and efficacy of drugs and are designed to meet regulatory standards, but they often take place in highly controlled settings that may not…

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CTEP Cloud Usage paper published in ACDMs Data Matters (Winter 2015)

Dec 22, 2016

White paper on cost of running NIS studies in the Cloud for Pharma..

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CTEP NIS paper published in SCDM Data Basics (Winter 2015)

Dec 22, 2016

White paper on rules to better data management and Pharmacovigilance in NIS

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Survey Results from over 460 Users in Russia

Dec 22, 2016

Collecting real world evidence in a local market is becoming increasingly important for a variety of reasons. It raises product awareness with local key opinion leaders (KOLs), gathers data to support health technology assessments, satisfies safety requirements for regulators and demonstrates the value of new medicines in the market.

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Tomas O’Mahoney presented at ACDM Conference 2015

Dec 22, 2016

CTEP’s Head of Operations Tomas O’Mahoney presented at the 2015 annual ACDM (Association of Clinical Data Management) Conference on the topic of non-interventional studies. Tomas presented his topic “Making BIG DATA smaller… Non intervention (NI) studies – 7 simple rules to better data management and 4+1 for improved pharmacovigilance in NI studies” at the industry-leading conference.

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CTEP ACDM paper entitled “PARAs must fit” published May 2012

Dec 15, 2016

Tomás O’Mahoney, Operations Director, writes in the Association for Clinical Data Management’s journal Data Matters on “PARAs must be fit”.

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