Medical Writing

We offer med­ical writ­ing ser­vices for a wide range of doc­u­ments that meet the high demands of the reg­u­la­to­ry process­es involved in the devel­op­ment of drugs, med­ical devices or nutri­tion­al prod­ucts. ICRC-Wey­er has the expe­ri­ence to sup­port you in plan­ning, coor­di­nat­ing and struc­tur­ing your clin­i­cal data. We offer a ful­ly inte­grat­ed med­ical writ­ing ser­vice in com­bi­na­tion with qual­i­fied sci­en­tif­ic con­sult­ing with respect to data pre­sen­ta­tion and interpretation.

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Our writ­ing experts com­bine pro­fes­sion­al writ­ing skills with a thor­ough under­stand­ing of ICH, EMA, FDA, MDR and EFSA  guide­lines and of regulatory/publishing process­es. All our med­ical writ­ers are mem­bers of the Euro­pean Med­ical Writ­ers Asso­ci­a­tion (EMWA).

Medical Writing Services

  • Clin­i­cal Study Protocols

  • Clin­i­cal Inves­ti­ga­tion Plans

  • Clin­i­cal Eval­u­a­tion Plans

  • Clin­i­cal Study Reports

  • Patient infor­ma­tion & Informed eCon­sent Forms

  • Investigator’s Brochures

  • Com­mon tech­ni­cal doc­u­ments (CTD), oth­er formats

  • Tech­ni­cal doc­u­ments for med­ical devices

  • Sci­en­tif­ic com­mu­ni­ca­tion mate­ri­als (mar­ket­ing and train­ing materials)

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Con­tact us and get an impres­sion of our dynam­ic team and way of think­ing. We are look­ing for­ward work­ing with you soon.