List of Services


ProScribe provides writing services to medical, marketing
academic and biotech / allied health organisations.

A list of ProScribe's services is shown below:

 

 
 



Medical

  • Clinical Study Reports 
        - to ICH standard
  • Investigator's Brochures 
        - to ICH standard
  • Clinical Study Protocols
  • Manuscripts for Peer-Reviewed Publications 
        - to CONSORT standard; working with your       company-nominated specialist as appropriate
  • Product Information Sheets /Consumer    
    Medicine
  • Information Sheets
  • Systematic Reviews / Literature Reviews
  • Standard Operating Procedures
  • Monitor's Manual / Case Report
        - Form Completion Guidelines
  • Newsletters
        - for clinical trial site staff, clinical trial       participants, intra-company profile of medical       department
  • Disease Summaries 
        - customised with relevant Australian detail for       therapeutic area training; excellent for       regional staff
  • Drug Summaries
        - utilising ProScribe's "a picture tells       a thousand words" method for rapid       comprehension
  • Ethics Submissions
  • Clinical Trial Summaries
        - for Sales & Marketing colleagues, ethics 
          committees, clinical trial participants
  • Investigator Meeting / Selection Meeting Minutes
  • Preceptorship Training Programs 
        - conducted by specialists in a hospital       environment to provide intensive, customised       therapeutic area training for CRAs and Project       Managers
  • Strategic Plans for Australian Affiliate 
        - for Clinical Research Managers / Medical       Directors seeking to raise the profile of their       department and Australian clinical research to       Head Office colleagues
  • Independent Review of Company Documents 
        - reviewed for grammar, punctuation, clarity       and structure; particularly valuable for       documents where the writer is “too close” to       the information or where documents have       been drafted overseas
  • Websites
        - ProScribe can prepare scientific / medical
          text for websites.  Please contact
          ProScribe for further details


Academia

  • Manuscripts for Peer-Reviewed Publications 
        - to CONSORT standard
  • Abstracts / Posters / Slide Presentations
  • Clinical / Nonclinical Study Reports
        - to ICH / GLP standard
  • Investigator's Brochures
        - to ICH standard
  • Clinical Study Protocols
  • Ethics Submissions
  • Congress / Scientific Meeting Proceedings
        - at the State, National or International level
  • Clinical Trial Manuals
        - for Investigators, Research Coordinators
  • Clinical Trial Summaries
        - for Trial Participants, Ethics Committees,          Hospital Annual Reports and Public Relations       Literature
  • Standard Operating Procedures
  • Systematic Reviews
  • Literature Reviews
  • Patient Education / Support Group Literature
  • Presentations on "Drug Development and Clinical
    Research"
        - for hospital / university staff not involved in       clinical research
  • Preceptorship Training Program
        - coordination of specialised educational              programs, delivered by academic staff in       hospital settings, for fee-paying       pharmaceutical industry staff; an additional       revenue stream for highly regarded academic       institutions
  • Strategic Plans for Attracting Industry
        - Sponsored Clinical Research
  • Websites
        - ProScribe can prepare scientific / medical
          text for websites.  Please contact
          ProScribe for further details
   

Marketing

  • Company Commissioned Articles 
        - a "one stop shop" from inception to completion,       including concept design, planning, writing, editing,       layout and publication
  • Advisory Board Minutes / Presentations
  • Scientific Meeting / Symposia Proceedings
  • Manuscripts for Peer-Reviewed Journals
        - to CONSORT standard; working with your company-      nominated specialist as appropriate
  • Abstracts / Posters / Slide Presentations
  • Medical Communication / Publication Strategic Plans
  • Systematic Reviews
        - now regarded as the highest level of evidence to       provide to prescribers - above randomised, placebo-      controlled trials
  • Clinical Expert Reports
        - working with your company-nominated specialist as       appropriate
  • Treatment Guidelines Publications
        - working with your company-nominated specialists as       appropriate
  • Product Monographs
  • Post Marketing Surveillance Study 
        - Protocols / Reports (as per APMA Code)
  • Competitor Analyses and Reports
  • Disease Summaries 
        - customised with relevant Australian detail; for Sales       Representatives, Product Managers & Patient Support       Groups
  • Drug Summaries 
        - utilising ProScribe's "a picture tells a thousand words"
          method for rapid comprehension
  • Clinical Trial Summaries
        - for Sales Representatives, Product Managers &       Patient Support Groups
  • Preceptorship Training Programs 
        - conducted by specialists in a hospital environment to       provide intensive, customised therapeutic area       training for Sales Representatives, Product       Managers or Registrars.
  • Patient Education / Support Group Literature
  • Websites
        - ProScribe can prepare scientific / medical
          text for websites.  Please contact ProScribe for further 
          details





Biotech & Allied Health

  • Investigator's Brochures
        - to ICH standard
  • Clinical Study Protocols and Clinical Study Manuals
        - for Investigators, Research Coordinators
  • Standard Operating Procedures
  • Manuscripts for Peer-Reviewed Publications
        - to CONSORT standard
  • Clinical Trial Documents
        - required by Regulatory Authorities / Ethics       Committees to conduct clinical trials (eg. CTX, CTN,       IND)
  • Clinical / Nonclinical Study Reports
        - to ICH / GLP standard
  • Abstracts / Posters / Slide Presentations
  • Clinical Consultancy 
        - including evaluation of clinical trial programs and       potential clinical trial investigators / institutions;
          assistance with submissions for regulatory authorities       [e.g. FDA, TGA, EMEA>
  • Preclinical Consultancy
        - including assistance with submissions for regulatory       authorities [e.g. FDA, TGA, EMEA> and the preparation
          of laboratory SOPs, nonclinical protocols and study
          reports to GLP standard
  • Systematic Reviews; Literature-Based Submissions
  • Performance Reports 
        - to demonstrate achievements and attract funding       from major pharmaceutical companies
  • Congress / Scientific Meeting Proceedings
        - at the State, National or International level
  • Websites
        - ProScribe can prepare scientific / medical
          text for websites.  Please contact ProScribe for further 
          details


 

 
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