The OPIS Medical Affairs Unit is team of experienced people with on average 15 years of experience and professionally qualified with scientific/medical degrees (MDs, PhDs).
Medical writers have strong scientific knowledge in most major therapeutic areas and possess a deep understanding of applicable regulations/guidelines to work in close collaboration with sponsors, methodologists and operational teams internationally.
OPIS provides the following services:
- Preparation of clinical trial documentation
- Study synopsis and protocol development
- Investigator Brochures
- Informed consent forms, letter to GP, patient cards, and other patient material
- Preparation/adaptation of clinical documentation in local language
- Clinical Study Reports
- Manuscripts and publications
Our Medical Affairs Unit offers medical support, in close collaboration with our biometrics team to ensure high-quality data and on-time reporting of study deliverables
Our Medical experts are also involved in the development of scientific manuscript and abstracts, publications and posters. Literature searches/reviews as necessary to obtain background information for the development of documents.
OPIS offers medical-scientific oversight of research activities:at OPIS the Medical Review is performed by an experienced Medical Advisor (physician) on critical study data (medical review of eligibility, concomitant medication/medical conditions, review of subject safety-related data, SAE narrative review, medical data coding and review) according to the requirements of the sponsor. OPIS Medical Affairs team is used to work within multidisciplinary project teams in compliance with regulatory requirements for quality management, in order to increase data quality and integrity of any clinical trial to the level required for valid conclusions on product performance.
Whether you are Sponsor, a Clinical Research Professional or an Investigator contact us to learn more about how we can help.