Blog

Considerations in rare disease study design

17/11/2022

Designing a clinical trial is a complex and challenging process. There are several key factors that researchers have to consider, from patients, costs, practicalities, risk measures and much more. Designing clinical trials for rare disease studies can be especially challenging. Rare disease research comes with its own unique challenges, making it particularly important to overcome […]

Read More

What is Research and Development in the Pharmaceutical Sector?

11/11/2022

Pharmaceutical R&D is a crucial process in the development of safe and effective drugs for market use. Funded by a blend of private and public sources, it plays a vital role in advancing medical treatments globally. In this article, we’ll delve into the world of Pharmaceutical Research and Development, exploring its evolution from past to […]

Read More

Clinical Trial Data Management: Explained

11/11/2022

Clinical data management (CDM) is one of the most integral processes in any clinical study.  Data is at the heart of research and clinical trial management. Without proper management, the research simply cannot provide the necessary data for successful drug evaluation.  Clinical data management (CDM) therefore ensures that the research gathers a sufficient level of […]

Read More

Writing a protocol for clinical research

08/09/2022

A clinical research protocol is one of the most vital components of any study.  It describes an overview of the research, including the main objectives, study design, and key considerations. It also ensures the safety of study participants and maintains the integrity of clinical data. The protocol document must be reviewed and approved before the […]

Read More

What are Good Laboratory Practices (GLP) and Guidelines?

08/07/2022

Good Laboratory Practice (GLP) is a set of criteria used to ensure quality assurance in non-clinical studies. GLP principles are concerned with the organisational processes by which studies are planned, performed, monitored, recorded, reported and archived. These guidelines are intended to support the integrity of safety testing data for products regulated by government agencies. GLP […]

Read More

How are Oncology Clinical Trials Different from Other Therapeutic Areas?

05/05/2022

Oncology is an area of medicine and clinical research that focuses on the study, treatment, prevention and management of cancer. Like other therapeutic areas of research, oncology treatments undergo testing in clinical trials. Clinical research in oncology has advanced the effectiveness and safety of cancer therapies, providing hope to millions of cancer patients worldwide.  Oncology […]

Read More

What Causes Drugs to Fail in Phase 3 Clinical Trials?

05/05/2022

Scientists investigate thousands of new drug ideas each year. Whilst many of these ideas are taken through to clinical stages of development, not all drugs successfully make it to market.  There are 3 main stages of clinical trials: phases 1, 2 and 3. At the end of each phase, investigators and regulatory authorities evaluate whether […]

Read More

Got a question?
Get in Touch or Submit an RFI/RFP

Our team is on hand to answer any questions you might have relating to the work we do at Simbec-Orion. Just fill in the form below, making sure to tick the boxes that apply, and we’ll respond as quickly as we can.

Looking to volunteer for a clinical trial?

Visit our dedicated volunteer website here, or email [email protected]

Follow us on Social Media

Name(Required)
Opt In Emails