cochrane systematic review writing services uk



Systematic Review

A systematic review is designed to summarise the results of available studies and provides a high level of evidence-based findings on the effectiveness of interventions. Our experts can handle any type of research, whether you need a systematic review based on controlled clinical trials or a review based on observational study designs or community (e.g. psychology) intervention. Our experts at Pubrica, perform a rigorous systematic review by following a multi-step process, which includes


(a) Identifying a well-focused clinically relevant research question while following suitable frameworks including PICO, SPICE, SPIDER, and ECLIPSE, etc.

(b) Developing a detailed review protocol with strict inclusion and exclusion criteria and registering the protocol at different registries such as The Campbell Collaboration, The Cochrane Collaboration, OSF Preregistration, SYREAF-systematic reviews for animals and food, Research Registry, Joanna Briggs Institute (JBI) and PROSPERO.

(c) A systematic literature search of multiple databases (including PubMed, Embase, MEDLINE, Web of Science, and Google Scholar) in finding relevant references that further require extensive search and study. Several other electronic databases and bibliographic sources will also be searched. Sources we posit for use for the project include:


  • Scientific literature databases as described above and others

  • Cochrane Library

  • Database of Abstracts of Reviews of Effectiveness (DARE)

  • NHS Economic Evaluation database

  • Material referenced in Publications obtained in the course of research on the topic

  • International Network of Agencies for Health Technology Assessment (INAHTA) documents

  • Clinical trials databases, including clinical trials, register.EU (EU), clinicaltrials.gov (US), and others.


However, using multiple databases to search relevant studies is laborious and time-consuming so a well-designed search strategy will be developed.

(d) Meticulous study identification using a variety of search terms, checking for a clear outcome (primary and secondary)

(e) Systematic data abstraction, by at least two sets of investigators independently,

(f) Risk of bias assessment with the use of existing different assessment tools (e.g. STROBE). For example, allocation concealment (selection bias), incomplete outcome data addressed (attrition bias), and selective reporting (reporting bias).

(g) Thoughtful quantitative synthesis through meta-analysis where relevant. Besides informing guidelines, credible systematic reviews and quality of evidence assessment can help Identify key knowledge gaps for future studies.


We can help you with the most used qualitative systematic review, as well as, quantitative, health policy and management information and meta-analysis.

Our systematic review at Pubrica is more structured at every stage of writing, and we ensure to critically check the rigor using standard methodological checklists such as PRISMA, CASP, AMSTAR, and ARIF, etc., based on the checklist provided.



  • Further, the general structure is presented as follows: 

Formulate the research question

Search for studies

Selection of studies

Data collection

Methodological quality assessment

Findings are interpreted.

The time required for producing a quality systematic review

Our Experts:

Pubrica Healthcare and Medical Research Experts provide custom scientific research writing and analytics (data science & biostatistics) services with a team of experienced researchers and writers available round the clock and ready to assist you with systematic review writing. We have PhD-level domain experts who also have decades of scientific writing experience. As such, we can deliver a high-caliber, written literature review. Our experts are very facile around scientific literature databases to complete the literature review, including PubMed & Medline and cancer domain expertise to selectively identify impactful journal articles to draw upon for the review. Written status reports will be shared at every milestone completion including
1) an overview of the status of completion of deliverables including specifics of the literature search and environmental scans;
2) a description of progress addressing discrete components of the Report as agreed;
3) describe challenges encountered, potential risks, and associated mitigation strategies.


Contact Our UK Medical Author’s;

Our email id – sales@pubrica.com

Contact No. +91 9884350006


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