Accomplishing access through value communication. That's what we do. PFG MedComm is a strategic market access consultancy that is a certified woman- and minority-owned and led organization that specializes in leveraging value communication to achieve access goals. We’ve transformed the traditional agency model, our unique approach takes a holistic 360° view that considers the entire development lifecycle when planning for market access. Our proprietary process involves anticipating challenges, adapting strategic plans, and accomplishing access through seamless execution combined with wraparound engagement. As a full-service strategic market access agency, our capabilities run the gamut from the earliest stages of clinical planning and strategy through launch, training, and beyond. We are experts in developing end-to-end marketing strategies and tactics across all healthcare stakeholders, ranging from various types of payers (governmental, commercial, employer) and HEOR to healthcare professionals and patients. Our team has a broad range of experience in supporting medical, payer, and HEOR communication strategy across pharmaceutical, biotech, medical device, and digital therapeutic companies. Over the past ten years, the PFG MedComm team has supported over 60+ brands (including 33 launches both US and global) across 50+ indications within 20+ therapeutic categories. Let's talk about what we can accomplish together.

PFG Stealth is a strategic consultancy for startups across the healthcare ecosystem (health tech, biotech, wellness, and medical). Capabilities: Go-to-market strategy, market access, launch planning, health economics and outcomes (HEOR), product development, value communication and value proposition development

As a team lead within the Value Communications groups, provide guidance on strategic scientific communications and publication plans; develop a variety of scientific communications materials including manuscripts, congress abstracts/posters, health authority communications, clinical study reports, and slide decks.

Provide independent freelance medical writing and editing services for pharma projects for various clients including pharmaceutical ad agencies and life sciences firms.

As a scientific Methods Expert, identified key requirements to ensure complete accuracy and compliance of ELN procedures using StarLIMS.

As a Scientific Application Specialist, led the development of Velquest procedures for use in analytical, clinical and preclinical labs at Bristol Myers-Squibb.Worked with scientists, lab managers, and analysts from analytical, clinical and preclinical laboratories at three different BMS sites (US and UK) to define parameters and effective workflow for lab procedures specific to each department.

As an Information Analyst Scientist, developed chemical monographs for publication in the 15th edition of The Merck Index to reflect current scientific, medical and technological uses of compounds for most effective home or medical use.

As the Regulatory Review consult, provided final review and approval of all information in major product websites, and related product collateral. Worked with Promotional Review Committee to review and approve various promotional and marketing materials prior to launch. Performed regulatory review of new websites at proposal stage and in test environment prior to launch, and responsible for regulatory review and audit of existing website content.

Authored a technical report submitted to internal and federal departments for review and implementation in the Microbiology Quality Control Lab.

As a summer intern in Oncology Biology, conducted research to analyze levels of HDAC expression as an indicative factor of cancer development.Project 1 : HDAC expression profiling in pre-cancerous and cancerous tissuesProject 2 : Processing and analysis of clinical trial samples