Medical Writing
We have experience in merging data and regulatory requirements into compliant documentation across the entire life cycle of the device.
Regulatory documents for clinical investigations
We support you in writing all documents required in a clinical investigation or clinical evaluation process. Our experts utilise templates and forms to ensure the completeness and regulatory compliance of these numerous documents.
Publications
We write scientific manuscripts, conference presentations and marketing materials. We start by evaluating the best strategy to use available data for the specific target group.
Contact us for more information
Meeri Säily
Sales Director, Consulting and Clinical Trials
meeri.saily@labquality.com
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Latest news
25/04/24 17:11
Meet us at RAPS in Berlin on May 6-8!
Visit our booth TB1 in the RAPS exhibition and hear about regulatory affairs services for and MD/IVD manufacturers.Read more
05/04/24 15:04
Meet us in Tomar, Portugal
Labquality will attend SPML's (Sociedade Portuguesa de Medicina Laboratorial) 16th scientific meeting in Tomar, Portugal, from 12 to 13 April 2024.Read more
25/03/24 11:10
Meet us at ECCMID in Barcelona
Visit our booth E5 in the ECCMID exhibition and hear about EQA services for microbiology, as well as CRO services for pharmaceuticals and MD/IVD manufacturers.Read more
14/03/24 17:29
Why Modeling Data Flows Is Needed in Clinical Investigations
data management manager explains how data flow modeling will help keep clinical investigation stakeholders informedRead more
05/03/24 10:37
EQA Coordinator Anna-Riitta Vanhanen Retires After 34 Years of Service
EQA Coordinator Anna-Riitta Vanhanen is retiring in the autumn of 2024 after working at Labquality since 1990. Biochemist Hanna Heikkilä will take over Anna-Riitta's EQA rounds.Read more
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