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pharmaceuticals

26 procedures tracked

Amendment to Regulation (EU) 2018/782

2025/2573(RPS)

Commission Proposal

European solidarity: key to securing medicine access in a shifting geopolitical era

2026/2727(RSP)

1st Reading (EP)

Critical Medicines Act (CMA)

2025/2568(RSP)

1st Reading (EP)

Malaria Combat

2005/2531(RSP)

1st Reading (EP)

Multiple Sclerosis

2007/2570(RSP)

1st Reading (EP)

Medicinal products subject to medical prescription (amendment of Directive 2001/83/EC)

2008/0256(COD)

1st Reading (EP)

Developing Countries: Vaccine Access

2009/2720(RSP)

1st Reading (EP)

Flu Epidemic

2009/2602(RSP)

1st Reading (EP)

Pharma Package & Health

2009/2506(RSP)

1st Reading (EP)

Access to Life-Saving Medicines

2014/2831(RSP)

1st Reading (EP)

Medicine Shortages

2020/2581(RSP)

1st Reading (EP)

Comirnaty Vaccine Authorisation

2022/2941(RSP)

1st Reading (EP)

Granting marketing authorisation under Regulation (EC) No 726/2004 of the European Parliament and of the Council for

2022/2928(RSP)

1st Reading (EP)

The annual renewal of the conditional marketing authorisation for the medicinal product for human use "Veklury -

2022/2661(RSP)

1st Reading (EP)

Gardasil 9: Marketing Objection

2023/2623(RSP)

1st Reading (EP)

2022 Discharge: EMA

2023/2156(DEC)

Adopted

The market of Northern Ireland

2023/0064(COD)

Adopted

EU Global Health Strategy

2023/2642(RSP)

1st Reading (EP)

Respiratory Infections & Drug Shortages

2023/2510(RSP)

1st Reading (EP)

Pharmaceuticals in Environment

2019/2816(RSP)

1st Reading (EP)

EMA Seat Location

2017/0328(COD)

Adopted

2016 Discharge: EMA

2017/2154(DEC)

Adopted

2016 Discharge: IMI 2

2017/2184(DEC)

Adopted

GMP: Human Medicinal Products

2017/2684(RPS)

Commission Proposal

Falsified Medicines

2008/0261(COD)

Adopted

Pharmacovigilance (Amendment)

2008/0257(COD)

Adopted