RegulatoryID Newsletter

Midyear Filing Deadlines to Plan For

RegulatoryID June 2026 monthly newsletter coverMonthly issue
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This month brings ten reporting and registration updates across U.S. and international jurisdictions, with deadlines on June 30 and July 1. The summaries below cover who is affected, what is due and where it is filed. Subscribers get the full requirements, source links and submission details for each.


UNITED STATES

Connecticut PMF Registration & Report Due 6/30

A pharmaceutical manufacturer that employs a pharmaceutical sales representative must register annually with the Department of Consumer Protection (the Department) as a pharmaceutical marketing firm. Registrations must be renewed annually by June 30.

Additionally, pharmaceutical marketing firms must provide the Commissioner of Consumer Protection (the Commissioner) with a report for the previous calendar year describing the activities of pharmaceutical representative(s).

Waterfront homes among autumn trees in Connecticut

Key Date

June 30, 2026

Filing Authority

Department of Consumer Protection


UNITED STATES

Connecticut APRN Report Due 7/1

Drug, device, biological and medical supply manufacturers must report transfers of value made to Advanced Practice Registered Nurses (APRNs) who are independently practicing (i.e., practicing not in collaboration with a physician in the state) by July 1 annually for the preceding calendar year.

Shingle-style homes on the Connecticut shoreline at sunset

Key Date

July 1, 2026

Filing Platform

DCP.DrugManufacturers@ct.gov


UNITED STATES

Massachusetts Pharmaceutical Code of Conduct Due 7/1

Massachusetts pharmaceutical and medical device manufacturers that sell or market prescription drugs or devices in the state must comply with the Massachusetts Marketing Code of Conduct and annually renew their registration by July 1, including payment of the $2,000 fee and compliance attestation. Manufacturers must also submit a transparency/disclosure report by July 1 for reportable payments or benefits of $50 or more made to covered recipients in the prior calendar year, using required Massachusetts company and covered recipient IDs.

Office towers rising over a Massachusetts city in late afternoon light

Key Date

July 1, 2026

Filing Platform

pharmameddata@massmail.state.ma.us


UNITED STATES

Florida Miami-Dade Lobbyist Expenditures Report Due 7/1

Drug, device, biological and medical supply manufacturers must report transfers of value made to Advanced Practice Registered Nurses (APRNs) who are independently practicing (i.e., practicing not in collaboration with a physician in the state) by July 1 annually for the preceding calendar year.

Palm trees along a sunny street in Florida

Key Date

July 1, 2026

Filing Platform

Lobbyist Online Registration Information System


UNITED STATES

D.C. Prescription Drug Marketing Cost Report Due 7/1

Prescription drug manufacturers and labelers that employ, direct or utilize marketing representatives in D.C. must report to the Department of Health their marketing costs for prescription drugs in the District for the preceding calendar year. Reports must be submitted annually via email by July 1.

Washington Monument rising behind office buildings in Washington, D.C.

Key Date

July 1, 2026

Filing Authority

DC.Accessrx@dc.gov


International

EFPIA Disclosures Due 6/30

Under the European Federation of Pharmaceutical Industries and Associations (EFPIA) Code of Practice, members of EFPIA must disclose by June 30, 2026, direct or indirect transfers of value (ToVs) made during the prior calendar year to healthcare professionals (HCPs), healthcare organizations (HCOs) and patient organizations (POs). Commencing 2026, EFPIA requires companies use a standardized template structure for methodological notes accompanying disclosed 2025 ToVs. 

European street corner with cafe awnings and a lit Metropol sign

Key Date

June 30, 2026

Filing Platform

Determined by Associated Code


International

MedTech Europe Disclosures Due 6/30

Under the MedTech Europe Code of Ethical Business Practice Disclosure Guidelines (“Disclosure Guidelines”), MedTech member companies must disclose all educational grants made during the prior calendar year to healthcare organizations (HCOs) registered or based in the MedTech geographic area by June 30. An update to the Disclosure Guidelines requires companies to gear up for a new disclosure process MedTech will instate in 2027.

Wooden houses along a lake in a European alpine village

Key Date

June 30, 2026

Filing Platform

Transparent MedTech


International

Mecomed Disclosures Due 6/30

Member companies of Mecomed must annually disclose educational grants made during the previous calendar year to healthcare organizations (HCOs) and professional conference organizers (PCOs) based or registered in the Mecomed geographic area by June 30 via the Mecomed central platform, Mecomed Disclosure.

Modern glass towers on a Middle Eastern city skyline

Key Date

June 30, 2026

Filing Platform

Mecomed Disclosure


International

Greece Disclosures Under Both Law and Industry Code Due 6/30

Companies engaged in covered interactions with healthcare providers (HCPs) or healthcare organizations (HCOs) based in Greece must annually disclose by June 30 to the National Organization for Medicines (EOF) relevant benefits granted directly or indirectly as required under Greek Law 4316/2014. In practice, the EOF has applied this disclosure obligation to companies producing products under jurisdiction of the EOF, which includes both pharmaceutical products and medical devices. Members of the Hellenic Association of Pharmaceutical Companies (SFEE) must also disclose information regarding relevant transfers of value granted to HCPs, HCOs and patient organizations (POs) by June 30.

Whitewashed village on a cliff above the sea at dusk in Greece

Key Date

June 30, 2026

Filing Platform

Law – EOF Central Platform | Code – Company Website


International

Lithuania Disclosures Under Both Law and Industry Code Due 6/30

Companies with market authorization, or their representatives, in the Republic of Lithuania must submit information about transfers of value (ToVs) provided to healthcare or pharmaceutical specialists and specified legal entities to the State Medicines Control Agency (VVKT) under the Law on Pharmacy by June 30. Additionally, members of the Innovative Pharmaceutical Industry Association (IFPA) and the Medicinal Product Manufacturers Association (VGA) must disclose information regarding relevant ToVs to healthcare professionals (HCPs), healthcare organizations (HCOs) or patient organizations (POs).

Red tiled rooftops of an old town in Lithuania

Key Date

June 30, 2026

Filing Platform

Law – vvkt@vvkt.lt | Code – Company Website


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