Your Trusted Partner in Medical Affairs and Medical Education

Our Services

Providing strategic support to commercial teams by delivering medical insights and participating in Promotional Medical Marketing Material (MLR) reviews to ensure adherence to FDA guidelines and industry standards.
Conducting clinical & technical competitive intelligence analyses and developing treatment landscape reports supporting New Product Launch Stretegies for highly competetive markets.
Supporting partners with Standard Operating Procedures (SOPs) and Work Instructions (WIs) to ensure audit readiness and quality standards.
Conducting audits and generating vendor training to ensure compliance with quality standards and performance metrics.
Publication planning support to map out communication plans that deliver key messages to key audiences.

Developing and overseeing drug information content focused on the safety and efficacy of pharmacotherapy for disease treatment, tailored for healthcare professionals.
Creating Continuing Medical Education (CME) materials for healthcare professionals, addressing knowledge, information, and performance gaps while ensuring alignment with learning objectives.
Ensuring scientific accuracy, validity, and regulatory adherence by integrating FDA safety alerts and product label updates into educational materials.
Reviewing systematic literature and the latest clinical guidelines to extract key insights for evidence-based medicine content generation.
Crafting patient-oriented materials that inform individuals about medical conditions, treatment options, and preventive strategies, by translating complex medical concepts.
Developing scientific and academic content, including manuscripts, journal articles, abstracts, posters, and slide decks.
Conducting literature searches and providing fact-checking and editing services for medical content.
Supporting the development of sales training modules and video/podcast scripts.

Medical Information Call Center (MICC)

Drafting and reviewing MICC materials, including Frequently Asked Questions (FAQs), Standard Response Documents (SRDs), and Product Information Requests (PRIs), to address medical inquiries and provide customized responses.
Resolving escalated and complex medical information requests from health care providers, third party payors, and PBMs.
Ensuring effective communication and exchange of safety information related to Adverse Drug Reactions (ADRs) and Product Quality Complaints (PQCs), in collaboration with stakeholders.