Learn How We Can Help Your Organization to Optimize Science with Technology

Our Domain Focus and Expertise

Technology & Managed Services

Support Digital Transformation Across the Pharma Value Chain

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Clinical Research Services

Accelerate Patient- centric Biopharma and Medical Device Clinical Development

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Manuscript Writing and Research support

Development of all types of manuscripts and end to end research support

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BioTexTers Workflow

Data review

A first stage-review and analysis of the raw data happens
to ensure that it is complete, accurate, and relevant to the manuscript being developed.
We work with closely with our clients to clarify any ambiguities or gaps in the
Data.

Manuscript Planning

Plan the manuscript, including outlining the sections of the
manuscript, identifying key messages, and determining the appropriate target for submission.

Writing & Editing

Based on the manuscript plan, we assign a team of medical writers and editors to draft the manuscript. The writers will use the raw data to write the methods, results, and discussion sections of the manuscript, while the editors will review the manuscript for clarity, accuracy, and adherence
to the target’s guidelines and policies.

Review & Feedback

Once the manuscript is drafted, we share it with our clients for review and feedback. We solicit comments or suggestions for revisions,
which will be incorporated by our experienced editors.

Finalization

Once all revisions have been made and the manuscript has been approved, we finalize the manuscript for submission to the target. This may involve formatting the manuscript, preparing figures and tables, and ensuring that all citations and references are accurate.

Submission & Post-submission Support

We also assist our clients with the submission process, including tracking the status of the manuscript, responding to reviewer comments, and revising the manuscript
as needed – end to end Project Management services are also provided.

Doing the right thing,
at the right time.

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Years Academic experience

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Research publications

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High impact Research Projects

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PhD students

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Scientific Experts

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Patents files and in-pipeline

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International conferences

Portfolio

Medical Writing

We offer a comprehensive range of medical writing services including scientific manuscripts of all kinds, clinical study reports, regulatory documents, prepare research proposals, scientific abstracts and posters.

Scientific Editing

Provide high-quality editing and proofreading services for scientific manuscripts as per requirement of all top rated journals, ensuring that the language is clear, concise, and accurate. Emphasize the use of industry-standard guidelines and checklists for editing.

Publication Planning

Assist pharmaceutical companies in planning the publication of their research findings, including identifying suitable journals and conferences, preparing abstracts and manuscripts, and managing the submission and review process.

Regulatory Writing

Offer regulatory writing services for pharmaceutical companies seeking FDA approval for their products. This includes preparing Investigational New Drug (IND) applications, New Drug Applications (NDAs), and other regulatory documents.

Scientific Consulting

Provide scientific consulting services to pharmaceutical companies, including literature reviews, gap analyses, and recommendations for future research directions. Emphasize experience working with pharmaceutical companies of all sizes and with a range of therapeutic areas.

Medical Communications

Offer a range of medical communications services, including slide decks, training materials, and educational resources. Highlight experience working with medical affairs teams to create engaging and informative content.

Grant Writing

Assist pharmaceutical companies in preparing grant proposals for funding from government agencies and private foundations. Emphasize experience with the grant application process and knowledge of funding opportunities in the pharmaceutical industry.

Translation Services

Provide translation services for scientific manuscripts, ensuring accurate and culturally appropriate translations for international publications. Highlight experience working with translators and reviewers in various languages.

Clinical Trial Design

Provide expertise in designing clinical trials for pharmaceutical companies, including protocol development, statistical analysis planning, and data interpretation. Emphasize experience working with regulatory bodies and adherence to industry standards.

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