Scientific, medical, and patient advocacy conferences and meetings represent critical opportunities and inflection points for life science companies throughout the year during all phases of development and the product lifecycle….
The FDA, through the Center for Drug Evaluation and Research (CDER), imposes strict regulations on the pharmaceutical industry for every aspect of drug development and marketing for products in the…
Med Communications’ Scientific Communications staff applied a dedicated work model to provide seamless support for the MI initiatives of a large global pharmaceutical company. A top 10 pharmaceutical manufacturer with…
At Med Communications, publication development and review is a cornerstone of our Scientific Communications offerings. Our comprehensive services span a wide range of publication types, including primary and secondary manuscripts…
With our efficient and flexible staffing models, Med Communications is equipped to navigate uncertainty while maintaining stability for our clients. Our skilled Scientific Communications team of healthcare professionals is agile…
In recent years, digital innovations have led to reimagined customer communications in the pharmaceutical industry. Interactive standard responses offer an enriched presentation of data that leads to a more tailored…
Advisory Boards provide life science companies with the unique opportunity to strategically engage with a forum of Key Opinion Leaders (KOLs) or Key External Experts (KEEs) on a range of…
AMCP formulary dossiers provide managed care organizations and health care decision makers with the information they need for formulary and medical policy coverage or reimbursement considerations. These dossiers include comprehensive…
Med Communications’ Scientific Communications Development and Review team identified significant accuracy issues and referencing errors during a routine review of a client’s existing field medical training slide decks. A rare…
Experience matters, particularly when it comes to producing high-quality, balanced scientific documents. Strict regulations govern every aspect of the U.S. drug development and marketing process to ensure that accurate, fair-balanced,…
