LOBBYIST

Justin Pine

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6ACTIVITIES
1ORGS REPRESENTED
14BILLS

Organizations represented

1

Orgs whose LD-2 filings list Justin as an active lobbyist, sorted by activity volume.

Biotechnology Innovation Organization6 activities

Bills they file on

14
H.R. 16722 mentions
H.R. 12622 mentions
H.R. 9462 mentions
S. 8642 mentions
S. 8541 mention
S. 10971 mention
H.R. 14921 mention
S. 5261 mention
S. 5271 mention
S. 10961 mention
S. 10951 mention
S. 7051 mention
S. 21151 mention
H.R. 43071 mention

Topics in Filings

173

Policy topics Justin files on across all their LD-2 activities.

FY 2025 Appropriations×20
FY 2026 Appropriations×13
Bio COMPETES×11
House GOP RFI on Supply Chain×8
Interagency Patent Coordination and Improvement Act×7
Show all 173 topics (+168 more) ▾
Prescription Pricing for the People Act×6
Preserve Access to Affordable Generics and Biosimilars Act×5
Stop STALLING Act×5
National Coverage Determination×5
BIOSECURE Act×4
Restrictions on Intellectual Property Rights×4
ORPHAN Cures Act×4
Pharmacy Benefit Manager Transparency Act×4
CMMI Authority×4
TRIPS Waiver×3
Development and Procurement Issues×3
Risky Research Review Act×3
Tropical Disease Priority Review Voucher×3
Development and Procurement×3
Funding for Strategic National Stockpile×3
FY 2026 Appropriations Funding for Antimicrobial Resistance×3
Monoclonal Antibody Coverage and Utilization×3
Prohibiting Adversarial Patents Act×2
Protecting Americans Data from Foreign Adversaries Act×2
Patent Eligibility Restoration Act×2
WHO Pandemic Preparedness Accord World Intellectual Property Office×2
Treaty on Intellectual Property×2
Genetic Resources, and Associated Traditional Knowledge World Trade Organization×2
340B Drug Discount Program×2
Executive Order on Access to Affordable Life-Saving Medications×2
Accelerated Approval Artificial Intelligence×2
Biosecurity Infrastructure for Operational×2
Biosimilar Copay×2
Interchangeability and Pharmacy Substitution×2
MINI Act×2
Climate Change×2
House GOP RFI on Data Privacy×2
Decentralized Clinical Trials×2
Promising Pathway Act×2
COVID-19 Lessons Learned×2
FDA Hiring Flexibility Drug Importation Drug Manufacturing×2
Quality & Distribution×2
Advanced Manufacturing×2
Drug Shortages×2
Safe, and Secure American Bioeconomy×2
Supply Chain Integrity and Traceability×2
Patent Thickets×2
Maintaining Investments and New Innovation×2
COVID-19 Pricing Related Provisions×2
Patient Cost-Sharing and Implementation×2
Strengthening Innovation in Medicare and Medicaid Act×2
MCM PRV×2
Advanced Research Projects Agency for Health×2
Alternative Payment Arrangements for Gene Therapies×2
Average Manufacturer Price Calculations×2
Coverage of Accelerated Approval Products×2
Drug Benefit Design×2
Encouraging Innovation Benefit Design to Lower Costs for Seniors Act×2
Pricing and Rebates×2
Value-Based Purchasing×2
National Defense Authorization Act×2
SUPPORT Act×2
Non-Opioid Analgesics×2
Coverage and Reimbursement Orphan Drug Issues×2
Give Kids a Chance Act×2
Pediatric Priority Review Voucher Program×2
R&D Funding for Medical Countermeasures×2
WHO Pandemic Preparedness Accord×2
HELP Copays Act×2
Administration Rebate Rule×2
Medicare Part B Physician-Administered Products×2
Patient Cost-Sharing and Smoothing×2
Protected Classes×2
Support of Patient Premiums and Cost-Sharing Obligations×2
Value-based Contracting and Communications Vaccines and Infectious Diseases×2
Adult Immunization×2
Countermeasures Injury Compensation Program×2
Maternal Immunization×2
MCM Manufacturing & Capacity×2
MCM PRV Reauthorization×2
Vaccine Injury Compensation Program×2
Vaccine Safety and Quality×2
Vaccine Safety net and Vaccine Infrastructure×2
Value of Vaccines and Vaccine Confidence×2
VICP Loopholes×2
Biodefense Research×2
Gene Editing×2
MCM PRV Program×2
HHS Reorganization×2
Pioneering Antimicrobial Subscriptions to End Upsurging Resistance×2
Funding for Biodefense/Biomedical/Emergency Preparedness Research×2
Pharmacy Benefit Managers Artificial Intelligence×1
Patentability of AI-Aided inventions Bayh-Dole Act/Tech Transfer×1
Invent Here×1
Make Here Act×1
Bayh-Dole Act×1
March-In Rights×1
Reasonable Pricing Clause Compulsory Licensing Data Privacy Issues×1
American Privacy Rights Act×1
Inventor Diversity for Economic Advancement×1
Drug Patenting×1
Affordable Prescriptions for Patients Act×1
Medication Affordability and Patient Integrity Act×1
Bill to address patent thickets×1
Title 35 to Address Infringements of Patents Claiming Biological Products×1
Protecting Consumer Access to Generic Drugs Act×1
FTC Orange Book Delisting Initiative×1
Orange Book Listing×1
PTO Proposed Rules on Terminal Disclaimer Practice×1
China Patent Reform×1
Patent Litigation Reform×1
USPTO Request for Comments: Experimental Use Defense 89 Fed×1
Reg 53963 Patenting of Biological Inventions×1
Section 101 Modernization×1
RESTORE Patent Rights Act×1
World Health Organization×1
Program & Oversight×1
American Pandemic Preparedness Plan×1
MCM PRV Program Reauthorization×1
NDAA×1
Reasonable Pricing Clauses in BARDA Contracts×1
CICP×1
White House National Biodefense Strategy×1
WHO Pandemic Preparedness Accord Biosimilars×1
Reimbursement Cell & Gene Therapy×1
FY 2026 Appropriations Data Privacy×1
Diversity & Inclusion×1
Clinical Trial Diversity Drug Evaluation and Review×1
Compounded Medicines×1
PBM Reform×1
VICP×1
CICP Funding for FDA×1
User Fees Funding for Health Resources and Services Administration×1
Funding for Womens Health Research International Reference Pricing Medicaid×1
Medicaid Drug Rebate Program Rule×1
Orphan Drug Tax Credit Pandemic Preparedness×1
Drug Supply Chain Management×1
Supply Chain Issues×1
Temporarily Refundable R&D Credit×1
Medical Countermeasures PRV Reauthorization×1
Lower Costs×1
More Cures Act×1
Vaccine and Antimicrobial Resistance Product Development and Incentives×1
State Strategic Stockpile Act×1
Executive Order on Achieving Efficiency Through State and Local Preparedness×1
Womens Health Research Pandemic Preparedness×1
340B Accountability Act×1
Program Implementation & Oversight×1
BSUFA Negotiations×1
General Cell & Gene Therapy×1
FY 2026 Appropriations Clinical Trial Data in China Data Privacy×1
General Diversity & Inclusion×1
Clinical Trial Diversity×1
General Drug Evaluation and Review×1
Compounded Medicines Drug Patenting×1
FY2025 Appropriations×1
PBN Reform×1
International Reference Pricing Foreign Drug Data Protection Laws×1
Regulatory Harmonization Funding for Antimicrobial Resistance×1
FY 2026 Appropriations International Reference Pricing Issues×1
Medicaid Drug Rebate Program×1
Innovation and Pediatric Drugs Act×1
Orphan Drug Tax Credit×1
CFIUS and Foreign Investment Drug Importation Drug Pricing×1
China Biotechnology Regulations×1
EU Ag-Biotech Policies×1
International Consistency of Regulation for Gene Edited Products×1
Korea Biotechnology Regulations×1
B5 Coalition on Supply Chain Resiliency×1
Medical Supply Chain Resiliency Act×1
Synthetic Biotech Pharmaceutical and Ag Biotech Tariffs US-China Trade Agreement×1
Ag-Biotech Provisions×1
IP Provisions World Health Organization×1

Pulled from the org’s own LD-2 disclosures. See the source filings ↓

Issue mix

LDA general-issue codes weighted by activity count.

Copyright/Patent/Trademark1
Health Issues1
Homeland Security1
Medical/Disease Research/Clinical Labs1
Medicare/Medicaid1
Trade (domestic/foreign)1