PMS Registry
In order to understand if there is other unknown side effect during the clinical trail, the PMS (Post-Marketing Study) will be conducted to learn more treatment experiences on patients, and collect their information for further study.
No. 9 of IRPMA COP Benchmarks regulates that all PMS shall go through JIRB, IRB or Ethics Committee and must be registered on the website of IRPMA PMS registry system. It is to ensure the studies conducted on patients have been approved by JIRB, IRB and protect patient’s right of privacy. The public can also get the information and objective of the PMS through the registry system.
Company Name
Title of Study
Update Date
Novartis (Taiwan) Co., Ltd. A Prospective, Non-interventional, Multi-center, Surveillance Study to Observe the Tolerability of Exjade® (Deferasirox) in Patients with Myelodysplastic Syndrome (MDS) for Chronic Transfusion-Related Iron Overload 2016-01-06
Novartis (Taiwan) Co., Ltd. Retrospective, non-interventional, multi-center study evaluating safety of fingolimod in patients with multiple sclerosis in Taiwan 2016-01-05
Pfizer Inc. Post-Marketing Surveillance study to observe INLYTA® treatment dosing pattern, safety and effectiveness in Taiwan real world routine practice 2015-11-25
Novartis (Taiwan) Co., Ltd. A 12-week treatment, multi-center, randomized, double-blind, double-dummy, parallel group study to assess the efficacy and safety of switching from salmeterol/fluticasone to QVA149 (indacaterol maleate/glycopyrronium bromide) in symptomatic COPD patients 2015-11-23
Novartis (Taiwan) Co., Ltd. An observational, multi-center, prospective, open-label study to assess effectiveness, safety and tolerability of treatment with single pill combination of vildagliptin plus metformin(50mg/500mg, 50mg/850mg, 50mg/1000mg film-coated tablets)in type 2 diabetes mellitus patients in a real-world setting 2015-11-12
Chugai Pharma Taiwan Ltd. Efficacy and safety evaluation of tocilizumab monotherapy in Taiwan population 2015-08-18
Boehringer Ingelheim Taiwan Limited GLORIA-AF: Global Registry, on Long-Term Oral Anti-thrombotic TReatment In
PAtients with Atrial Fibrillation. (Phase II/III)
Bayer Taiwan A non-interventional, global, cross-sectional study to Check Atrial Fibrillation rates in patients 65 years or older by means of a device for opportunistic screening 2015-05-21
Pfizer Inc. A Phase 3b/4 Randomized Double Blind Study Of 5 mg Of Tofacitinib With And Without Methotrexate In Comparison To Adalimumab With Methotrexate In Subjects With Moderately To Severely Active Rheumatoid Arthritis 2015-04-29
Bayer Taiwan Co., Ltd. Xarelto® for Long-term and Initial Anticoagulation in Venous Thromboembolism (VTE) in Latin America, EMEA and Asia 2015-04-29
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