ILUVIEN has been has granted marketing authorization in Norway for the treatment of vision impairment associated with chronic diabetic macular edema (DME) considered insufficiently responsive to available therapies and has been approved for reimbursement in Portugal for the same indication.
What does MA stand for?
MA stands for Marketing Authorization
This definition appears very frequently and is found in the following Acronym Finder categories:
- Business, finance, etc.
See other definitions of MA
We have 141 other meanings of MA in our Acronym Attic
- Manual Assist (nursing)
- Manufacturing Approval
- Map Analysis
- Maranhao (Brazil)
- Maranhão (Brazilian state)
- Margin Agreement
- Marijuana Anonymous
- Marin Academy (California)
- Maritime Administration
- Market America (independent entrepenurial corporation founded by James H Ridinger)
Samples in periodicals archive:
An announcement is made by Takeda Oncology Company and Takeda Pharmaceutical Company Limited conditional marketing authorization for ADCETRIS for two indications: (1) the treatment of adult patients with relapsed or refractory CD30 positive Hodgkin lymphoma (HL) following autologous stem cell transplant (ASCT) or following at least two prior therapies when ASCT or multi-agent chemotherapy is not a treatment option, and (2) for the treatment of adult patients with relapsed or refractory systemic anaplastic large cell lymphoma (sALCL).
Lancet Oncology Editor Comments on EU Conditional Marketing Authorization
First Application for Marketing Authorization in European Union
Taro," NASDAQ: TARO) reported today that Taro Pharmaceuticals (UK) Limited ("Taro UK"), its affiliate in the United Kingdom, has been granted a marketing authorization for Etopan XL Tablets 600 mg, Etodolac ("Etopan XL") by the Medicines and Healthcare Products Regulatory Agency, the UK equivalent of the U.
The Mutual Recognition Procedure is a pan-European regulatory procedure to obtain marketing authorizations in European Union countries based on mutual recognition of marketing authorization in one member EU country (Reference Member State).
The European Marketing Authorization for Evoltra[R] (clofarabine) is for "the treatment of acute lymphoblastic leukemia (ALL) in pediatric patients who have relapsed or are refractory to at least two prior regimens and where there is no other treatment option anticipated to result in a durable response.
PhotoCure ASA, Oslo, Norway, has announced that the Australian Drug Evaluation Committee (ADEC) has recommended extension of the current marketing authorization for Metvix to include the treatment of basal cell carcinoma (BCC, the most common type of skin cancer).