Stay Up to Date on The Latest News Regarding Covid-19 |
Wells Health Group is a Health Policy Consulting and Government Relations Firm Based in Washington D.C.
WHG Helps Clients Navigate an Unprecedented Number of New Federal Emergency Regulations - The COVID-19 Reality & Beyond
Wells Health Group Areas of Expertise
COVID-19 Reality - New Federal Regulations - Post Outbreak & Beyond
WHG Specializes In Health Policy Consulting For Life Science Companies To Help Maximize Stakeholder Value:
|
WHG Helps Clients Navigate an Unprecedented Number of New Federal Emergency Regulations
|
COVID-19 Reality - Impact on Budget Neutrality
|
Wells Health Group - Innovators in Health Policy
WHG's innovative approach to health policy consulting is built on a two-step sequential process founded on 70+ years successful healthcare industry and government relations experience:
WHG provides clients a systematic and targeted engagement by working sequentially through interconnected groups of analytics to verify solid sustainable health policy strategies and reimbursement pathway tactics.
|
Why Our 70+ Years Industry & Government Relations Experience Matters
- Because we come from the healthcare industry - WHG is uniquely positioned to best understand our client’s challenges and develop targeted government relations’ strategies.
- Because of our government relations experience representing industry we knew it was critical for WHG to have a Washington D.C. presence.
- Because WHG is strategically located on Pennsylvania Avenue between the Capitol and the White House and just six blocks for the main HHS building, WHG has been able to more readily access face-to-face meetings at multiple levels of the HHS Agencies and on Capitol Hill.
- Because WHG's previous years of Washington D.C. presence with face-to-face meetings at multiple levels of the HHS Agencies and on Capitol Hill, we are a known entity and know how to leverage virtual access to multiple levels of the HHS Agencies and on Capitol Hill.
The U.S. healthcare delivery system, unlike any other industry and unlike any other country's healthcare system is:
Pre and Post Pandemic Outbreak - Health policy decision-making guidance and reimbursement methodologies are primarily driven by federal government initiatives (HHS, CMS, CDC, FDA & NIH) and generally adopted by commercial payers.
|
Pandemic Health Policy Challenges That Effect CMS Reimbursement, CDC Guidance, FDA Market Access and NIH Infectious Disease Research
On February 4, 2020, the HHS Secretary determined that there is a public health emergency that has a significant potential to affect national security or the health and security of United States citizens living abroad, and that involves the virus that causes COVID-19. On the basis of this determination, the Secretary then declared that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of the virus that causes COVID-19.
In continuing response to the COVID-19 pandemic, on March 24, 2020, and based on the February 4, 2020 HHS EUA determination, the HHS Secretary declared that circumstances exist justifying the authorization of emergency use of medical devices, including alternative products used as medical devices, due to shortages during the COVID-19 outbreak. EUAs for home collection kits reference this declaration. |
The Emergency Use Authorization (EUA) authority allows FDA to help strengthen the nation’s public health protections against CBRN threats by facilitating the availability and use of MCMs needed during public health emergencies.
Under section 564 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), the FDA Commissioner may allow unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions caused by CBRN threat agents when there are no adequate, approved, and available alternatives. |
FDA Emergency Use Authorization (EUA), FDA Approval or FDA Clearance allows for commercialization. It does not mean that a product is covered or eligible for reimbursement by Medicare, Medicaid, or commercial insurance.
FDA assigned product categories determine a companies commercialization pathway; Emergency Use Authorization (EUA), FDA Approval or FDA Clearance
FDA approved or authorized indications for use and FDA product coding can result in downstream consequences with significant reimbursement pathway implications.
FDA controlled regulations affect CMS controlled policies determining site of care utilization, benefit category, coverage criteria and payment mechanisms.
|
CMS reimbursement processes, CDC guidance, FDA regulations and NIH expanded research
Federal Regulations are not intuitive and can lead to uncertainties and market access complications especially during the HHS Emergency Use Authorization (EUA) authority
Federal Regulations are not intuitive and can lead to uncertainties and market access complications especially during the HHS Emergency Use Authorization (EUA) authority
Wells Health Group Consulting Services
Health Policy Consulting - WHG's innovative approach is built on a two-step sequential process.
Strategy Analytics - Comprehensive Medicare, Medicaid and commercial insurance reimbursement pathway analysis.
Reimbursement Pathways – We identify the foundation of reimbursement hurdles and opportunities.
|
DC Based Government Relations - WHG understands the nuances of how the Administration, Congress and Federal Agencies shape healthcare policy.
The WHG team’s years of healthcare industry and government relations experience positions us uniquely to best understand our client’s challenges and develop targeted government relations strategies.
Health Policy Legislation - In Congress at least 6 different full committees and their respective subcommittees have appropriations, jurisdiction and oversight responsibility over healthcare.
Health Policy Implementation - HHS - CMS - FDA have multiple centers, offices and administrative contractors with regulatory oversight and often-overlapping jurisdiction over healthcare reimbursement coding, coverage and payment methodologies.
|
Evaluating CMS Reimbursement Pathways, CDC Guidance and FDA Market Access Corridors - One of the most critical and challenging analytics of healthcare M&A due diligence
WHG can help clients prepare for a successful due diligence process.
How well is the client positioned for funding or coverage challenges and the inevitable shift from fee-for-service to value-based payments?
WHG understands the health policy challenges and misconceptions that can affect transactions.
WHG help's clients evaluate a transaction’s potential to maximize stakeholder value based on real-life experiences.
|