Maze House Medical

A professional regulator medical writer with wide experience in clinical research.

A passion for presenting information in a readily accessible way appropriate to the target audience.

Clinical study reports, clinical protocols, and safety narratives, and a wide range of other regulatory documents and medical communications prepared to a high standard.

Extensive experience in the pharmaceutical industry, contract research organisations, and academia.

Duncan J Currie

BSc PhD

Medical writing

Maze House Medical Ltd

Maze House Medical Ltd provides medical writing consultancy services to the pharmaceutical and healthcare industries. We enable our clients to reach their medical writing requirements by supplying quality medical writing documents within the agreed timeframe, at a competitive price. We strive to create strong and trusting partnerships with our clients to ensure that their demands are satisfactorily met, to the highest standard, and on time.

We take great pride in our ability to present complex scientific material accurately and clearly with a focus on depicting information in a readily accessible way highlighting the appropriate key messages to form valid, compelling, and concise conclusions.

About Duncan J Currie

Duncan is the director of Maze House Medical Ltd, which he founded in 2011. He is a senior medical writer with extensive experience in pharmaceutical companies and contract research organisations with a track record of delivering a range of high-quality regulatory documents within tight deadlines and budgets.

His key strengths are writing clinical study reports, clinical protocols, and safety narratives. He also has a wide range of experience in other regulatory documents and in medical communications.

Duncan has been a freelance medical writer since 2011, providing medical writing consultancy services to a diverse range of clients.

Contact Maze House Medical:

Experience

Maze House Medical Ltd 2011 to date

Freelance Medical Writer
PPD 2008 to 2011

Senior Medical Writer
Quanticate 2007 to 2008

Senior Medical Writer
Pfizer 1997 to 2007

Senior Medical Writer
PRA International 1996 to 1997

Medical Writer
H Lundbeck 1995 to 1996

Medical Writer
HPRU, Surrey University 1991 to 1995

Research Officer/Fellow
Clinical Pharmacology Dept. Dundee University 1985 to 1991

Research Assistant

Regulatory Writing

Clinical Study Reports

Independently written clinical study reports produced for a wide range of therapeutic areas across all drug development phases in accordance with the appropriate regulatory guidelines, SOPs, and style. Clinical study report synopses also written for public disclosure.

Clinical Study Protocols

Protocol writing services for clinical studies of any scope or size and indication following appropriate regulatory requirements, SOPs, and style. I can also update existing protocols with protocol amendments as appropriate.

Safety Narratives

Writing of the full range of regulatory safety narratives to any level of detail as required for clinical study reporting.

Investigator Brochures

New or updated investigator’s brochures written according to requirements, collecting and compiling up to date information from the relevant suppliers.

Summary Documents

Compilation of clinical sections of the Common Technical Document.

Clinical Trials Registries

Submissions to EudraCT and Clinical Trials.gov

Quality Control

Quality Control checks and comprehensive document review.

Other Services

Manuscripts and Posters

Organisation of materials for scientific papers and abstracts for peer reviewed journals and production of posters for scientific or medical conferences and related destinations.

Advisory Board Minutes

Compilation of complete and accessible minutes from live advisory board meeting recordings.

Current and Previous Clients

"A very professional medical writer, delivering quality documents for our CSRs. He is very accessible and knowledgeable.”

I very much liked working together with Duncan for his flexibility with multiple changed project timelines, providing pro-active solutions to write the CSR, delivering high quality work and always delivering on time. Duncan is very professional and it was a pleasure working with him on my project!

Many thanks for the excellent and high-quality work on a large volume of patient narratives. Chiltern were delighted with your responsiveness, high quality and experience in both writing and QC of CSR patient narratives for this large and complex oncology study. We would most certainly work with you again on future projects. A pleasure to work with.

Duncan produced the minutes for a day long advisory board meeting in Nov 2021, on behalf of our client seeking input from subject matter experts for the design of an important oncology clinical study. The document was of high scientific quality, clearly written, and produced in a timely fashion and at a competitive cost. The client was very happy with the deliverable and required no changes. Duncan is a pleasure to work with, highly skilled and we were very satisfied with Duncan’s active contribution to the project. I would highly recommend his medical writing work and professional approach.

+44 (0) 1304 380035

+44 (0) 7712 290364