
Jonathan StevensJonathanStevens
Partner, Life Sciences & Healthcare
Jonathan Stevens is a partner in the Investigations & White Collar Defense practice. Prior to joining the firm's Orange County office, Jonathan was based in the firm’s Washington, D.C. office.
Jonathan was former in-house counsel for a multinational medical device company and has broad experience in the life sciences sector. He focuses his practice on government and internal investigations, regulatory and anti-corruption compliance counseling, and white collar litigation on behalf of pharmaceutical and medical device companies.
Conducted product launch readiness assessment and compliance counseling related to patient-focused initiatives and support programs, including reimbursement/field support, data management, digital patient support platforms, free product and bridge programs for various rare disease companies. Designing and vetting diagnostic and genetic testing programs offered by companies, including rare disease companies, to patients, including the test assay design, physician and patient messaging and disclosures, and data usage. Conducted comprehensive product launch readiness assessments for numerous pharmaceutical companies, tailoring control enhancements to evolving risk profiles associated with particular commercial, medical and market access operational plans and strategies. Conducted numerous global anti-bribery and anti-corruption risk assessment on behalf of pharmaceutical and medical device companies. Conducted numerous product launch readiness assessments on behalf of pharmaceutical companies. Conducted proactive compliance market reviews on behalf of multinational rare disease company in Spain, Portugal, Middle East and Brazilian markets. Conducted anti-bribery and anti-corruption due diligence associated with the multibillion-dollar acquisition of a multinational injectable drug and biosimilar company in the Brazilian market. Conducted anti-bribery and anti-corruption due diligence associated with the multibillion-dollar acquisition of multinational orphan drug company in the Brazilian market. Acted as regulatory advisor on behalf of private credit, direct lenders, finance companies and alternative and specialty lenders in both cross-border and U.S.-focused healthcare transactions.
Conducted product launch readiness assessment and compliance counseling related to patient-focused initiatives and support programs, including reimbursement/field support, data management, digital patient support platforms, free product and bridge programs for various rare disease companies.
"Compliance Lessons from DOJ’s Merit Medical Settlement," Law360, Co-Author
NOVEMBER 3, 2020
"Telehealth Considerations for Medical Device Manufacturers During and After COVID-19," Medical Device & Diagnostics Industry, Co-Author
OCTOBER 20, 2020
"5 Compliance Lessons from Novartis’ FCPA Settlement," Law360, Co-Author
JULY 13, 2020
"7 COVID-19 Compliance Areas for Life Sciences Companies," Law360, Co-Author
MAY 4, 2020
"Key Healthcare Compliance Governance Essentials for Small and Mid-Size Life Science Companies," Orange County Business Journal, Co-Author
OCTOBER 14, 2019
"The Rise of Anti-Corruption Whistleblowers in Latin America," Global Investigations Review, Co-Author
DECEMBER 7, 2018
"Time to Clean Up: As Operation Car Wash Progresses, Are Medical Device and Pharmaceutical Companies Out of Time with Brazilian Authorities?" Paul Hastings Client Alert, Co-Author
MAY 18, 2017
"A Special Type of Government Scrutiny: Pharmaceutical Manufacturer Relationships with Specialty Pharmacies: Part II." Bloomberg Law, Co-Author
APRIL 7, 2017
"A Special Type of Government Scrutiny: Pharmaceutical Manufacturer Relationships with Specialty Pharmacies: Part I," Bloomberg Law, Co-Author
MARCH 29, 2017
- University of Florida Levin College of Law Global Corporate Compliance LAW6090
- Compliance for Innovative Therapies: A Spotlight on Rare Disease Companies CBI West Coast Compliance Congress, PresenterOCTOBER 22, 2019