Publishing your first paper
From choosing a title to handling the reviewers.
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Publication PlanningStrategic CommunicationsScientific CommunicationsMedical EducationMedical IllustrationGrant Applications and Project PartnershipFree, practical guides from Niche’s regulatory specialists and clinical teams, covering everything from bench to bedside.
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Three guides almost everyone finds useful.
From the first concept to the conference poster, the collection follows the work our teams deliver every day.
Shape the study and the evidence it needs
Sites, protocols, records and approvals
Keep the study and the team on track
Turn data into compliant documents
Get the science into the literature
Present and promote the work
Short series of guides that work best read together.
From choosing a title to handling the reviewers.
The groundwork that keeps a study on track.
The documents regulators and registries expect.
Filter by area or search by topic. Every guide is free to download.
35 guides
For regulatory and disclosure teams: registration, results reporting, CTIS and how to keep records consistent across registries.
Download the free guideFor anyone preparing or reviewing an IB: what a well constructed, fully compliant brochure needs to contain.
Download the free guideFor non-clinical teams: the quality system behind planning, performing, recording and reporting non-clinical studies.
Download the free guideFor medical writers and study teams: key learnings for delivering high quality CSRs on time.
Download the free guideFor study leads: how to design short, flexible protocols that can be reviewed and edited quickly.
Download the free guideFor clinical operations teams: how to identify investigator sites that will meet their study requirements.
Download the free guideFor anyone working on research studies: what GCP training records should contain and how to maintain them.
Download the free guideFor investigators and sponsors: the benefits IITs offer and the risks they carry.
Download the free guideFor early phase teams: what defining a healthy Phase I participant really involves, and why it matters.
Download the free guideFor medical affairs teams: how to plan advisory boards that close a real knowledge gap.
Download the free guideFor clinical experts: how consensus statements are developed when evidence is limited or lacking.
Download the free guideFor medical and commercial teams: how to find and profile the right experts in an appropriate, considered way.
Download the free guideFor authors and sponsors: the principles of authorship, ethics and transparency every paper should follow.
Download the free guideFor authors: how to choose the right journal first time and avoid delays, cost and rejection.
Download the free guideFor authors: how to write a short abstract that stands on its own and does your work justice.
Download the free guideFor authors: how to answer reviewer comments so your corrected manuscript is accepted.
Download the free guideFor authors: how to manage a journal rejection and move your manuscript forward.
Download the free guideFor research teams: how to navigate authorship decisions and avoid disputes.
Download the free guideFor authors and reviewers: how to stay safe and avoid unwarranted accusations of intellectual theft.
Download the free guideFor researchers: what the h-index and other bibliometric measures mean, and how to use them.
Download the free guideFor authors: how to plan and write a review that summarises the state of play in a field.
Download the free guideFor clinicians: how to write a case report that shares novel or relevant clinical insight.
Download the free guideFor researchers seeking funding: what separates successful grant applications from the rest.
Download the free guideFor writers and researchers: how to plan a search strategy that finds the right references.
Download the free guideFor medical writers: where AI tools can support your work, and where they should not.
Download the free guideFor authors: how to write the title readers see first, so your work gets noticed.
Download the free guideFor communications teams: the conventions that get a press release past the gatekeepers.
Download the free guideFor programme teams: how a well chosen name and identity raise awareness of a clinical programme.
Download the free guideFor anyone writing in pharma: how to assess and edit your own documents for clarity and accuracy.
Download the free guideFor study leads and managers: how to plan and run meetings that are worth everyone's time.
Download the free guideFor presenters: simple design rules for slides that communicate your message clearly.
Download the free guideFor conference presenters: how to produce a poster that looks professional and reads clearly.
Download the free guideFor organisers: the planning and organisation behind a successful scientific meeting.
Download the free guideFor researchers: how to disseminate your findings and build your profile beyond the journal.
Download the free guideFor PhD students: how to prepare for writing your thesis, so you know exactly what to expect.
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Sign up for new guidesThe specialists who write these guides also deliver the work: medical writing, regulatory affairs and clinical operations.
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