Medical and Scientific Communication - Overview
Are you bringing a new brand or product onto the market? Are you focused on the post-approval promotional requirements of a product? Does your company have an effective medical communication strategy, means, and channels to disseminate and consume scientific information?
Freyr brings Medical and Scientific Communication CoE expertise to empower the medical affairs and healthcare community. Freyr can be your partner in creating a medical communication strategy and executing it seamlessly to create larger benefits for all stakeholders, i.e., Healthcare Professionals (HCPs), Key Opinion Leaders (KOLs), consumers, and patients.
Freyr provides end-to-end solutions for Medical and Scientific Communication with a dedicated team of professionals who cater to the pharma industry. Freyr boasts of a team of seasoned scientific writers, complemented by an innovative design studio that skillfully crafts scientific content across diverse communication channels. Backed by a proficient Medical, Legal, and Regulatory (MLR) review team, we guarantee the substantiation and Regulatory compliance of content and claims.
Through Medical and Scientific Communication, Freyr creates all promotional and non-promotional assets that disseminate scientific data, clinical outcomes, Product Information (PI) and Instructions For Use (IFU), safety information, and disease and therapy awareness throughout the different phases of a product from pre-clinical, pre-launch to post-launch. Along with the abovementioned assets we also create assets for different target audiences or external stakeholders of the pharmaceutical industry.
Freyr’s Medical and Scientific Communication
Medical and Scientific Communication
- Quality control of the data and scientific information
- Develop or execute submission-related documents
- Support in addressing peer review comments
- Infographics for print and digital media
- Videos with infographics, animations, and demonstrations, including MOA videos and video abstracts
- Ensuring Regulatory compliance with country-specific guidelines established by Regulatory authorities such as FDA, EMA, MHRA, TGA, HSA, PMDA, ANVISA, LATAM, and Health Canada
- Verifying the material's accuracy and completeness of medical and scientific claims

- End-to-end content creation, design, and review services
- Quick TAT, high-quality communication assets
- Compliant with global promo and non-promo guidelines
- Tailored solutions as per client’s needs
- Modular content management
- Claims and reference/literature library management
- Experienced scientific writers and industry experts (Medics, PhDs, and Pharmacists)
- State-of-the-art design studio
- Leader of Regulatory solutions in the pharma industry
- ISO 9001 & 27001 certified
