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Medical Writing Services

By Catherine M Evans PhD, CMPP

Your experienced and reliable partner for high-quality

Face of Catherine M. Evans PhD, CMPP

As a professional medical writer since 2015, I offer services in medical and scientific communications as well as regulatory writing.

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I work with agencies, small biotech and start-ups, large pharma, medical and patient organisations and also individuals.​​

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My working language is English (native speaker).

Catherine M Evans PhD, CMPP

Badge showing status as a Certified Medical Publication Professional (CMPP)
Logo for members of EMWA for 2024
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Medical communications

Every medical affairs project has unique requirements. I love the diversity of work that's driven by the need to adapt communication to the user experience of healthcare professionals.

Field medical and MSL​
  • Interactive toolkits
  • Internal communications

  • Internal onboarding and training

  • Modular global resources

  • Objection handlers​

  • Proactive and reactive materials

  • Scientific platforms and narratives​​​

​​Advisory boards and expert panels

  • Agenda and slide development

  • Attendee invitations and communications

  • Minutes

  • Pre-meeting surveys

  • Tailored reports

​HCPs

  • Animations and infographics

  • Clinical trial explainers

  • Continuing medical education (CME) materials

  • Leave pieces

  • Mechanism of action animations/infographics

  • Multidisciplinary audiences

  • Onsite and online courses/conferences

  • Platforms (publications, disease awareness)

  • Publication extenders

  • Study aids

  • Webinars​​

Scientific communications

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Scientific communications

I craft concise content through language and data visualisation, while maintaining the accuracy and integrity of complex research so that science is communicated effectively.

Manuscripts and publications​​

  • Author management

  • Clinical practice guidelines

  • Clinical trial publications

  • Consensus reports

  • Narrative reviews

  • Management of patient authorship

  • Peer review and resubmission

  • Publication extenders

  • Strategic publication planning

  • Submission

  • Systematic reviews

  • White papers​

​Conferences and symposia​
  • Abstracts

  • Agenda development

  • Onsite materials including biographies

  • Onsite congress support

  • ​Minutes, proceedings and summary reports

  • Posters

  • Slide development and review

  • Speaker management

  • Voting management

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Regulatory writing

Through proactive project management and responsive communication, I drive development of high-quality clinical trial documentation to prioritise patient safety and advance medical innovation.

Documents

  • Clinical trial protocols

  • Clinical trial reports

  • Informed consent forms

Processes

  • Project management

  • Quality control

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More

Some skills and experience span many projects and don't fit neatly in the categories above. Here are some other responsibilities that I am familiar with.

Management​
  • Project management

  • Process development

  • Standard operating procedures

  • Strategic insight to align project with objectives

  • Style guide development

Patient-facing activities​

  • Blog articles and web content

  • Patients as publication authors​

  • Patient support programs

​Services​
  • ​​Document templates

  • Data QC

  • Editorial review

  • Reference mark-up

  • Veeva and Zinc annotation

  • Workshop planning and implementation

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